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Search Jobs by Category
| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Principal Scientist I/II - DMPK |
Minimum Requirements
· Ph.D. in a DMPK-related field plus at least 8 years experience in the pharmaceutical industry and in the DMPK discipline
· Experience in representing the DMPK discipline on cross-functional drug discovery project teams
· Demonstrated ability to influence, mentor and supervise staff working toward project progression and candidate delivery
· Thorough knowledge of the DMPK discipline and a successful track record of the application of DMPK principles to drug discovery
· Proven ability to develop and enhance a DMPK area of specialism
· Familiarity with DMPK-related lead identification and optimization techniques
· Familiarity with and commitment to the pragmatic application of DMPK data to the optimization of lead compounds
Skills and Competencies
· Strong leadership attributes and ability to leverage maximum potential from DMPK staff and to influence cross-functional drug discovery project team members
· Excellent team player and ability to work effectively with a variety of personalities
· Breadth and depth of knowledge of the DMPK discipline as it applies to the discovery and selection of high quality candidate drugs
· Strong scientific, strategic and organizational competency in discipline
· Breadth of knowledge and experience in the drug discovery arena
· Demonstrated ability to critically evaluate drug discovery problems and apply physico-chemical and DMPK tools and principles to achieve solutions
· Ability to martial and apply multi-disciplinary resources to achieve drug discovery goals
· Developed expertise in a specific sub-discipline of DMPK with the ability to communicate and apply this expertise to drug discovery challenges
· A focus on speed and delivery while maintaining quality of results
· Excellent verbal and written communication skills
Preferred Background
· Expertise in the principles of DMPK, in the application of experimental techniques to optimize and characterize the disposition of drugs and in managing senior level staff
 |
| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Translational Strategist - Infection Research |
| Degree level required and minimum years experience:
· A strong candidate would typically have a Ph.D. or M.D./Ph.D. and 10 or more years of experience, or equivalent experience, of which a minimum of 6 years should be in the pharmaceutical industry or other relevant setting
· Experience in anti-bacterial discovery and development is desirable
Competencies (knowledge and skills):
· Internally and externally recognized expertise in a scientific, technical or organizational area and the capacity to apply literature and theoretical concepts to the advancement of Infection portfolio goals.
· Possess strong problem solving skills and the ability to, on the basis of their own experience and analytical skills, ascertain the value of and initiate the use of new techniques for solving problems within and beyond their immediate project.
· Have a complete understanding of the AstraZeneca drug discovery and development process.
· Understand and work towards the AstraZeneca business objectives.
· Be highly productive: consistently generating high quality results within established time frames, even in areas of limited precedent.
· Possess strong knowledge and understanding of relevant database and scientific support software.
· Be a proactive communicator with excellent verbal and written communication and listening skills. Solicit opinions and feedback from others. Deliver presentations that are well thought out, informative and convincing. Able to present work at internal and external meetings when appropriate.
· Able to direct scientific staff and manage their performance.
· Able to effectively negotiate, persuade and influence others in a matrix environment.
· Capable of proposing and implementing scientific, technical or organizational ideas and initiatives.
· Able to manage multiple tasks efficiently, consistently generating high quality results within established time frames, even in areas of limited precedent.
Behaviors:
· Fosters environment of scientific excellence, innovation, productivity and timeliness, leading by example. Is reliable, has strong work ethic, and shows respect for colleagues
· Demonstrates leadership.
· Mentors and provides development opportunities for matrix or direct reports.
· Demonstrates commitment to team goals and consistently demonstrates influence in team & project meetings, advising project teams with respect to technical solutions and potential new approaches for consideration. Seeks solutions to issues that affect team morale and effectiveness
· Proactively shares expertise and ideas and is viewed as a resource by colleagues. Actively seeks to give advice and encouragement to the scientific community, promoting self as an approachable resource.
· Expands personal skills and knowledge as required to be effective. Demonstrates flexibility, open-mindedness, and adaptability. Projects creditability and professionalism. Is candid and honest in discussions
· Act in accordance with all AstraZeneca policies on personnel, SHE, best laboratory practice, etc.
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| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Principal Scientist; Medicinal Chemist |
| * Ph.D. in Chemistry
* 4-10 years experience post-PhD.
* Demonstrated ability to supervise and mentor other scientists preferably at the Ph.D. level.
* Must have thorough knowledge in synthetic organic and medicinal chemistry coupled with a proven track record in drug discovery.
* Must be familiar with lead identification optimization techniques employing parallel synthesis technology and rational drug design and virtual screening approaches to lead optimization.
* Must be familiar with the pragmatic application of DMPK data to the optimization of lead structures
* Experience in leading multi-disciplinary research groups through drug discovery efforts is preferred.
|
| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Associate Director DMPK (In Vitro) |
| Minimum Requirements:
· Ph.D. in a DMPK-related field plus at least 8 years experience in the pharmaceutical industry and in the DMPK discipline
· Experience in representing the DMPK discipline on cross-functional drug discovery project teams
· Demonstrated ability to influence, mentor and manage staff working toward project progression and candidate delivery
· Thorough knowledge of the DMPK discipline and a successful track record of the application of DMPK principles to drug discovery
· Proven ability to develop and enhance a DMPK area of specialism
· Familiarity with DMPK-related lead identification and optimization techniques
· Familiarity with and commitment to the pragmatic application of DMPK data to the optimization of lead compounds
Skills and Competencies:
· Strong leadership attributes and ability to leverage maximum potential from DMPK staff and to influence cross-functional drug discovery project team members
· Excellent team player and ability to work effectively with a variety of personalities
· Breadth and depth of knowledge of the DMPK discipline as it applies to the discovery and selection of high quality candidate drugs
· Strong scientific, strategic and organizational competency in discipline
· Breadth of knowledge and experience in the drug discovery arena
· Demonstrated ability to critically evaluate drug discovery problems and apply physico-chemical and DMPK tools and principles to achieve solutions
· Ability to martial and apply multi-disciplinary resources to achieve drug discovery goals
· Developed expertise in a specific sub-discipline of DMPK with the ability to communicate and apply this expertise to drug discovery challenges
· A focus on speed and delivery while maintaining quality of results
· Excellent verbal and written communication skills
Preferred Background:
· Expertise in the principles of DMPK, in the application of experimental techniques to optimize and characterize the disposition of drugs and in managing senior level staff
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Scientist - Neuroscience Biology |
| ·PhD plus minimum 2 years of post-doctoral research experience, demonstrated ability to implement independent research as evidenced by a strong publication record related to the desired core discipline.
Preferred Background:
·Behavioral Neuroscience or comparable discipline.
|
| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Alliance Administrator |
| Skills and Experience
? Undergraduate degree. BS in life sciences preferred.
? 2-3 years pharmaceutical/biotech strongly preferred.
? Knowledge of the pharmaceutical business, process and activities preferred.
? Knowledge of the disease areas, drug development activities and commercial processes within AZ preferred.
? Strong proficiency in Microsoft Office
? Excellent time management and organizational skills, detail orientation, and ability to multi-task in a high volume environment with shifting priorities.
? Strong interpersonal skills
- Contract management experience preferred.
Knowledge (Preferred)
? Understanding of the terms within a collaboration agreement
? Understanding of the process of establishing collaborative research ventures
? Understanding of AZ?s Discovery organisation
? Appreciation of EU, US funding systems
? Appreciation of other AZ Functions? activities
? Awareness of applicable RA research areas
? Awareness of drug discovery process
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Associate Director; Corporate Affairs-Brand |
| ? BS/BA degree in public relations or affairs, communications, marketing, or related field
? Minimum of 7-10 years experience in public affairs
? Previous track record for developing strategy for corporate affairs, direct media/spokesperson experience, interfacing with leadership within an organization
? Demonstrated success and effectiveness at delivering required outcomes in positions with ever-increasing levels of responsibility, authority, accountability and organizational impact
? Demonstrated understanding of and ability to perform effectively and successfully in the industry and in the environment in which it operates.
Skills and Competencies:
? Role-models leadership in the broader AstraZeneca context and is inspirational in translating AZ?s vision and what it means for his/her work unit
? Listens attentively and responds constructively to the needs, viewpoints, and interests of others. Effective communicator: verbal and written.
? Demonstrates strategic thinking, planning and strategic influencing capabilities. Communicates an aligned, clear vision for the future role of his/her own work unit with clearly focused priorities
? Effective team leadership and management abilities. Strives to improve cross-functional working and eliminate non-value adding activities
? Strong developer of organization, team, and individual. Expresses consistent commitment to company?s objectives, priorities and values by visible actions.
? Takes initiative, makes decisions, operates independently and is an effective team member, operates interdependently, builds consensus decisions
? Demonstrates general business literacy, knowledge and acumen along with demonstrated proficiency in functional/technical/professional discipline.
? Demonstrated ability to set and successfully manage to a budget.
? Comfortable and competent problem-solver; solution-oriented; not constrained by process or precedent
? Demonstrates ability to be influential by identifying key stakeholders, adapting approach to gain their commitment and delivering business objectives
Preferred Background:
? Pharmaceutical corporate affairs or product public relations experience in top pharma company
? PR agency experience desirable
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Brand/Country/SET Procurement Manager ? US Engineering |
| ? Degree or equivalent professional qualification
? Relevant work experience, including experience within Procurement
? People management experience
? Energetic and self motivated
? Strong written and verbal communication skills
? Oral and written fluency in Business English
? Ability to use a range of influencing techniques
? Proficiency in Microsoft Word, Power Point and Excel
? Proved ability to manage multiple projects/tasks effectively
? Proven experience of change management
? Demonstrated success working in a team environment
? Strong analytical skills
? Industry and commodity experience
? Professional Procurement qualification
? Proficiency in Procurement and other business related systems, e.g. ERP, Ariba
? Financial Analysis: Dun & Bradstreet reports and Credit Scoring
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Sr. Staff Veterinarian |
| Minimum Requirements
?DVM (or equivalent) and licensed to practice in the US or equivalent
?License to practice in at least one state in the United States
?ACLAM board certification or board eligibility
?1 to 5 years of laboratory animal medicine experience, with record of increased responsibilities and accomplishments, in either a pharmaceutical or academic environment
?Knowledge of regulatory requirements for the care and use of animals in research
?Experience working in a matrixed multidisciplinary environment and knowledge of the drug discovery and development process
?Effective communication, organizational and technical skills
?Strong interpersonal skills with an ability to collaborate and work in teams
?Ability to motivate others, positively influence people, and work in a team environment
|
| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Intern - Site Services and Logistics |
| Currently pursuing a four-year Bachelor degree in Architectural Engineering, Interior Design or Facilities Planning and Management. Would also consider Architecture, Construction Management or Civil Engineering majors. · Courses: Computer Aided Design, Technical drawing, Building Design and Construction · PC proficiency: AutoCAD, MS Office, MS Outlook Skills and Competencies: · Above average to excellent computer skills in AutoCAD, MS Office, MS Outlook; · Ability to read and understand architectural building floor plans, blueprints and construction documents; · Organized work environment skills and good understanding of documentation requirements; · Strong attention to detail; · Demonstrated analytical and troubleshooting skills, excellent safe work habits; · Strong oral and written communication skills; · Ability to follow procedures as dictated by SOP (standards of operation); · General working knowledge of laboratory or commercial building systems.
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Post-Graduate Intern |
| The minimum education, training and experience requirements for the role are:
-A Masters degree and/or a Ph.D. candidate in pharmaceutical sciences or chemical engineering (or related disciplines).
-Completed coursework with the necessary credits for a Masters or Ph.D. degree preferably with electives that would provide a sound theoretical background in the fields of statics, mathematical modelling, material properties etc.
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Patient Safety Principal Scientist Compliance and Support |
| Minimum Requirements ?Education and Experience:
?Qualified to degree level in biosciences or an equivalent healthcare or pharmaceutical industry background with proven competence in Patient Safety/Clinical Development
?At least 5 years Patient Safety and/or Clinical Development experience
?High level of technical competence, with an ability to balance this with industry standards to achieve business goals
?Proven leadership skills, able to resolve conflict
?Able to work with a high degree of autonomy
?Able to work effectively as a member of a cross-functional or global team
?Comprehensive understanding of Patient Safety regulatory obligations
?Able to represent AstraZeneca externally where required
?Able to acquire and assimilate knowledge in different disciplines, disease and therapeutic areas
?Demonstrable professional excellence ? adds value by applying expertise proactively
?Proven good communication skills with ability to work across cultures
?Able to influence whilst maintaining independent and objective views
?Maintains high ethical standards, including a commitment to AstraZeneca values and behaviors
?Good attention to detail
?Good time management
?Fluent in English
?Computer literate
Organizational Behaviors:
?Passion for Customers
?Drives Performance
?Works Collaboratively
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Procurement Leader - Commercial Procurement Account Mgmt |
| ? College degree required
? Minimum 10 years? work experience
? At least 5 years? experience of people management, including managing teams of senior professionals and managers and establishing performance expectations
? At least 5 years? customer facing or selling experience
? Exceptional skills in strategic influencing, collaboration, communications, and conflict management
? Project background in most, if not all, key categories of commercial spend, such as Agency, Media, Market Research, Medical Education, Conferences, Print, Premiums and Direct Marketing.
? Strong analytical skills, business acumen, drive for results and customer focus
? Energetic and self motivated
? Strong written and verbal communication skills
? Oral and written fluency in Business English Proficiency in Microsoft Word, Power Point and Excel
? Proved ability to manage multiple projects/tasks effectively, with proven prioritization skills
? Proven experience of change management
? Demonstrated success working in a team environment
Preferred Background:
? Advanced degree preferred in Science, Marketing or business related discipline
? Experience leading and participating on cross-functional and/or global teams
? Exposure to AZ Commercial functions and responsibilities.
? 3 years direct experience in purchasing, project and program management
o Procurement process knowledge, agreement management, financial analysis, market analysis, supplier analysis, supplier diversity, supplier management, technology utilization, strategic planning and integrated supply chain experience
o Proficiency in Procurement and other business related systems, e.g. ERP, Ariba
? Financial Analysis
- Dun & Bradstreet reports
- Credit Scoring
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Patient Safety Principle Marketing Company Support & Process Improvement |
| Minimum Requirements ?Education and Experience
?Qualified to degree level in biosciences or an equivalent healthcare or pharmaceutical industry background with proven competence in Patient Safety/Clinical Development
?At least 5 years Patient Safety and/or Clinical Development experience
?High level of technical competence, with an ability to balance this with industry standards to achieve business goals
?Proven leadership skills, able to resolve conflict
?Able to work with a high degree of autonomy
?Able to work effectively as a member of a cross-functional or global team
?Comprehensive understanding of Patient Safety regulatory obligations
?Able to represent AstraZeneca externally where required
?Able to acquire and assimilate knowledge in different disciplines, disease and therapeutic areas
?Demonstrable professional excellence ? adds value by applying expertise proactively
?Proven good communication skills with ability to work across cultures
?Able to influence whilst maintaining independent and objective views
?Maintains high ethical standards, including a commitment to AstraZeneca values and behaviors
?Good attention to detail
?Good time management
?Fluent in English
?Computer literate
Organizational Behaviors
?Passion for Customers
?Works Collaboratively
?Drives Performance
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Strategic Project Mgr |
| Minimum Requirements:
5-7 years of commercial pharmaceutical industry experience
Minimum of 3 years of project management experience.
Exceptional interpersonal, communication, leadership, and facilitation skills
Demonstrated proficiency in all Microsoft applications
Bachelor?s degree in Business, Business Administration, Marketing, Communication, Organizational Design, Human Performance, or other relevant discipline
Preferred Background:
- Pharmaceutical Marketing, Marketing Research, Change Management, or other relevant Commercial experience
- 5+ years of strategic/process/change management business consulting experience
- Demonstrated ability to lead and produce results in a matrix environment: ?Lead without Authority?
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Medical Director- Patient Safety- Respiratory and Infection/GI Therapy Area |
| Requirements ? Education and Experience
? Medical degree
? At least 2 years of clinical experience post-registration/certification
? High level of medical competence, with an ability to balance this with industry standards to achieve business goals
? Two or more years of Drug Development/Pharmacovigilance experience obtained while working in industry and/or academia
? A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities is preferred
Skills and Capabilities
? General medical/therapeutic area knowledge
? Ability to acquire and assimilate knowledge in different disciplines, disease and therapeutic areas
? Ability to influence whilst maintaining independent and objective views
? Excellent communication, interpersonal and organizational skills
? Attention to detail
? Delivery focus
Organizational Behaviors
? Integrity and high ethical standards
? Excellent team-working skills
? Ability to appreciate diversity and work as equals with global and cross-functional teams
? Customer-focused
? Demonstrable leadership skills in directing the work of others
Problem solving
? Manage a wide range of problems, requiring complex judgments and innovative solutions, needing well-developed conceptual thinking and thus having a high level of business risk management
? Access external resources for advice and respond to external events by adjusting plans or developing new approaches to working
Leadership Capabilities:
? Passion for Customers
? Thinks Strategically
? Acts Decisively
? Drives Performance
? Works Collaboratively
? Develops People and Organization
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Cardiac |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in cardiology/cardiovascular disease
· MD background with strong expertise in cardiology, ideally drug-induced cardiac injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Cardiac |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in cardiology/cardiovascular disease
· MD background with strong expertise in cardiology, ideally drug-induced cardiac injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Hepatic |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in hepatology
· MD background with strong expertise in hepatology, ideally drug-induced liver injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record.
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Renal |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in nephrology
· MD background with strong expertise in nephrology, ideally drug-induced kidney injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record.
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Scientist Bio Science |
| Minimum Requirements
?PhD plus minimum 2 years of post-doctoral research experience, demonstrated ability to implement independent research as evidenced by a strong publication record related to the desired core discipline.
Preferred Background
?Behavioral Neuroscience or comparable discipline.
Reporting Relationship
?Direct Reports ? none initially
?Indirect Reports - supervise a team of up to two colleagues
Leadership Capabilities
Passion for Customers: Understands one?s customers and uses that insight to provide value
Thinks Strategically: Quickly identifies and acts on opportunities, combining forethought with action. This is based on an understanding of the external environment and its impact on AZ.
Acts Decisively: Makes and acts on decisions quickly and effectively and fosters the same in others. This is based on an underlying courage to enable risk taking for the business.
Drives Performance: Holds self and others accountable for the achievement of performance expectations. Creates an environment that enables others to perform at their best.
Works Collaboratively: Actively creates and promotes cross boundary collaboration with the aim of archive better business results. Boundaries can exist between individuals, geographies, cultures, teams, functions or organisations.
Develops People and Organisation: Demonstrates and genuine commitment to the time and effort needed to develop oneself and others.
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Brand/Country/SET Sourcing Mgr-US FM Hard Services |
| ? Degree or equivalent professional qualification
? Sourcing Experience
? Energetic and Self Motivated
? Strong written and verbal communication skills
? Proficiency in Microsoft Word, Power Point and Excel
? Proved ability to manage multiple projects/tasks effectively
? Demonstrated success working in a team environment
? Strong analytical skills
? Strong organisational skills
? Proficiency in Procurement and other business related systems, e.g. ERP, Ariba
? Financial Analysis, e.g.: Dun & Bradstreet reports and Credit Scoring
|
| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Senior Associate Scientist ? Compound Management |
| Minimum years experience:
?Typically 3 or more years experience in a Biotech / Pharmaceutical setting post Bachelor's Degree or equivalent
Competencies (knowledge and skills):
?Well-developed understanding of theoretical aspects of discipline and a high level of ability in experimental techniques.
?Regularly demonstrates capacity to apply literature and theoretical concepts to the advancement of project goals.
?Strong knowledge and understanding of relevant database and analytical software.
?Independent planning, execution and interpretation of experiments that contribute significantly to project goals.
?Able to develop logical positions and convince others.
?Highly productive: consistently generates high quality results within established time frames.
?Strong problem solving skills and the ability to, on the basis of their own experience and analytical skills, initiate the use of new techniques and to ascertain their value in solving problems relating to their immediate project.
?Collects, analyzes, and summarizes data for reports and patents, and presents data at project and/or team meetings.
?Delivers presentations that are well thought out, informative and convincing. Able to present work at internal meetings and external meetings when appropriate.
?Communicates effectively with colleagues at all levels, showing well-developed verbal and written communication skills, coupled with an ability to listen, resulting in clear and succinct messages and accurate interpretation of feedback.
?Communicates relevant information from meetings or literature to colleagues.
?Identifies and rapidly informs supervisor and colleagues of issues critical to attainment of project goals and is realistic in ability to overcome problems.
?The ability to manage multiple tasks efficiently.
Behaviors:
?Is reliable, has strong work ethic, and respect for colleagues.
?Commitment to team goals.
?Willingly shares expertise and ideas and is viewed as a resource by colleagues.
?Is candid and honest in discussions.
?Demonstrates flexibility, open-mindedness, and adaptability.
?Act in accordance with all AstraZeneca policies on personnel, SHE, best laboratory practice, etc.
?Expands personal skills and knowledge as required to be effective.
?Projects creditability and professionalism
?Fosters environment of scientific excellence, innovation, productivity and timeliness by example.
Leadership Capabilities:
Passion for Customers: Understands one?s customers and uses that insight to provide value
Thinks Strategically: Quickly identifies and acts on opportunities, combining forethought with action. This is based on an understanding of the external environment and its impact on AZ.
Acts Decisively: Makes and acts on decisions quickly and effectively and fosters the same in others. This is based on an underlying courage to enable risk taking for the business.
Drives Performance: Holds self and others accountable for the achievement of performance expectations. Creates an environment that enables others to perform at their best.
Works Collaboratively: Actively creates and promotes cross boundary collaboration with the aim of archive better business results. Boundaries can exist between individuals, geographies, cultures, teams, functions or organisations.
Develops People and Organisation: Demonstrates and genuine commitment to the time and effort needed to develop oneself and others.
|
| Johnson & Johnson Family of Companies |
Miami |
FL |
11/19/2009
|
| Medical Director Complaint Handling & Safety Surveillance |
| M.D. degree is required for this role. Knowledge and experience within cardiology/radiology and/or drug safety or related activities is required. Five years experience in medical device/pharma vigilance activities is preferred. Basic knowledge of the medical device marketplace associated with successful experience in one or more of the following: clinical, regulatory, quality, customer service or technical applications is required. Ability to travel as needed or requested is required. The ability to use computers and computer based software is required. Current or previous leadership and management experience is preferred. |
| Johnson & Johnson Family of Companies |
|
MO |
11/19/2009
|
| Kansas City, MO: Professional Sales Specialist - LifeScan, Inc. |
| This position requires a 4 year degree, as well as, a minimum of 2 years of outside sales experience preferred. 3-5 years of sales experience in a healthcare professional sales environment or experience in professional diabetes care or related healthcare fields strongly preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. This position may require overnight and/or weekend travel. Excellent written and oral communication skills are essential. Preference will be given to candidates living within 30 miles of the territory, with documented history of proven sales success in outside sales, pharmaceutical, or medical products industry. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| 2009 Fall R&D Co-op |
| Candidate must be enrolled in an accredited college/institution and be in good academic standing Student must be pursing a BS or Graduate Degree in Mechanical Engineering, Materials Science and Engineering, Bioengineering, Electrical or related field. Must be available to work full time (40 hours/week) during the 2009 Fall semester. This position will be located in Somerville, NJ. |
| Johnson & Johnson Family of Companies |
Jacksonville |
FL |
11/19/2009
|
| SENIOR RESEARCH OPTOMETRIST |
| A minimum of an OD degree is required. A MS degree or Formal Corneal and Contact Lens residency program is preferred. A minimum of 2 years experience in clinical research of contact lens products is preferred. Very good oral and written communication skills are required. Knowledge, understanding and application of principles, concepts and practices of clinical research are preferred. Strong organizational, communication and analytical skills are preferred. The ability to manage multiple projects simultaneously is required. Experience with studies under IRB (Investigative Review Board) / Ethics Committee / or FDA (Food and Drug administration) review is preferred. Proficiency in Word, Excel, PowerPoint is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Jacksonville |
FL |
11/19/2009
|
| Manager Clinical Affairs |
| A minimum of a Bachelor's degree is required with a minimum of 8+ years of experience in the Clinical Research of medical devices or pharmaceuticals, or 12+ years equivalent work experience in the Clinical Research of medical devices or pharmaceuticals. Pharmaceutical specific experience is preferred. A degree in a science related discipline is preferred. Supervisory responsibilities or experience is an asset. Complete understanding and application of principles, concepts and practices of clinical research procedures will be required. Knowledge and experience with Good Clinical Practice (GCP) is required. Experience working with Regulatory Agencies is required. Opthalmic experience is an asset. Strategic and tactical Clinical and Business knowledge to gain approval and ensure maintenance of legal marketing status of all products will be required. Strong communication, organizational and interpersonal skills are needed. Broad based technical knowledge and skills in diverse areas of business (e.g. R&D, Operations, QA, laboratories, marketing, etc.) are an asset. Ability to effectively negotiate and influence peers, affiliates and Regulatory agencies to ensure that regulatory and business needs are met will be needed. Must have flexibility to provide innovative approaches to gain marketing approvals globally. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Cincinnati |
OH |
11/19/2009
|
| Quality Systems and Compliance Specialist |
| Minimum of a BS or BA in Business, applied Sciences, Quality or an Engineering-related discipline or equivalent work experience is required. CQA certification is strongly preferred. CQE and/or CRE Certification is also preferred. A minimum of 7+ years of total work experience in Regulatory Affairs and/or Quality Assurance in a medical device or pharmaceutical environment is required. Strong auditing skills are required. Experience managing or participating in internal audit programs is also required. Strong Project Management skills, excellent verbal and written communication skills, influencing management skills are required. Knowledge of ISO-GMPs is required. Knowledge of GLP, GCP Quality Systems and international requirements is preferred. Knowledge of design and development, labeling and manufacturing systems is required. Knowledge of continuous improvement principles is preferred. Experience and/or interactions with a Regulatory agency is preferred. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! Johnson & Johnson is committed to diversity and invites all interested candidates to apply for positions of interest. EOE M/F/D/V Please note: In order to be considered eligible for an interview, candidates must apply online through the appropriate web portal. |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Principal Scientist Veterinary Surgeon - Somerville, NJ |
| A DVM/VMD (from an AVMA (American Veterinary Medical Association) approved and accredited program) or equivalent degree is required. Board Certification is strongly preferred but not required. Surgical residency training and/or industry experience (minimum 3 years in industry without residency) is required. Scientific publications are required. Experience working in a team environment is required. Highly motivated, self-starting, and strong verbal and written communication skills are required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Staff Process Engineer |
| A minimum of a Bachelor's degree and a minimum of 9 years of engineering related experience OR a Masters degree and a minimum of 7 years of engineering related experience OR a Ph.D. and a minimum of 4 years of engineering related experience is required. Complex understanding of polymer and engineering fundamentals is required. Experience in a highly regulated industry is required. Experience in the medical device or pharmaceutical industry is an asset. A clear mastery of statistical and experimental engineering techniques is required. Proficiency with Microsoft Office, specifically Excel is required. Experience with Microsoft Project is preferred. Experience with balloon catheter process and polymer bonding is preferred. Experience with Six Sigma/Process Excellence Tools, Training, and/or Certification is preferred. Experience managing complex projects is required. Excellent verbal and written communication skills are required. This candidate will have strong analytical/problem solving skills. Ability to work on cross functional teams is required. The ability to develop and lead teams, strong collaborative skills, and the ability to negotiate and influence are required. This position will require that you be based in Menlo Park, CA and travel 10% of the time internationally and domestically. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Director Health Economics and Reimbursement SNS (Selective Nerve Stimulator) |
| A minimum of a Masters degree in biomedical science, health service research, business or economics is required. Post doctoral experience is also desirable. Health services research and clinical epidemiology experience preferred. At least 5 or more years experience in HE&R function in pharma, biotech, device or other relevant health care environment required. At least 2 or more years experience in device reimbursement required. Strong knowledge of the US and EMEA healthcare system. Prior experience interfacing directly with Evidence-based medicine and Research and development teams. Knowledge of the needs and expectations of regional payers, insurers and commercial customers in our strategic markets. Strong knowledge of evidence generation and value proposition strategy development used in R&D new product development process in order to provide support for price and market access. Experience in leading cross- functional teams to deliver and communicate evidence generation strategy and customer requirements. Experience with the methods and research tools used in Outcomes research, including clinical epidemiology, health economics and health series research. Ability to author, co-author, publish, referee and critique manuscripts relevant to product value. Demonstrated ability to provide constructive and innovative input into complex problems. Good judgment in business decision making. Ability to create a strategic plan by integrating short-, mid-, and long-term objectives. Ability to clearly communicate to a variety of audiences, both big picture ideas as well as technical details. A proven track record of being able to integrate their own thinking and activities into the work of other teams. Experience of developing concise and audience-focused communications, both written and for presentation. Project management experience. Ability to lead and support change. Significant accomplishments and leadership demonstrated internally; externally recognized as a credible peer/leader. Excellent communications and presentation skills; Excellent interpersonal skills. Ability to represent J&J in a leadership capacity at a variety of external forums. Customer centricity - ability and appreciation to clearly understand that customer and their unique needs; ability to translate understanding into effective development and delivery of relevant solutions. Must have skills in the following: Collaboration and teaming; Strategic Thinking; Ability to make sound business decisions; Intellectual Curiosity; ability to be results oriented. Up to 20% US-based travel is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Sr Engineer - R&D |
| BS degree in relevant discipline and at least five years of related engineering experience is required; or MS degree in relevant discipline and at least three years of related engineering experience. Experience in the medical device industry would be a requirement. Must possess the basic understanding of engineering fundamentals. English communication skills, written and oral is required.Experience with executing design control deliverables is also required. Experience with Cardio Vascular Products will be required in this role.If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Glendora |
CA |
11/19/2009
|
| PROGRAM MANAGER |
| QUALIFICATION REQUIREMENTS: The ability to lead a cross functional product development team is a requirement for this role along with the ability to strategize and plan for product development objectives. It will be a requirement to have experience with Stage Gate Product Development Process. Experience working with Design History Files is an asset along with knowledge of Regulatory or Clinical Requirements. NPD in Medical Device experience is a requirement. EDUCATION and/or EXPERIENCE: BA/BS or equivalent; and at least 4 years of related experience and/or training; or equivalent combination of education and experience. Master's degree or Ph.D. in the applicable field of Engineering would be an asset.If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
NJ |
11/19/2009
|
| R&D Co-Op- Fall 2010 |
| Candidates must be working towards a B.S., M.S., or PhD degree in Chemical Engineering, Materials (Science) Engineering, Biological or Biomedical Engineering, Biology, Chemistry, Pharmaceutical Sciences, or other related concentration. Candidates must possess a 3.0 GPA or higher. Candidates must be authorized to work in the U.S. for any employer. |
| Johnson & Johnson Family of Companies |
Glendora |
CA |
11/19/2009
|
| TEST LAB SUPERVISOR |
| Education and/or Experience: a Bachelors Degree in Electrical/Mechanical Engineering or related field with a minimum of 5 years industry experience and 3 years medical device experience. It is also required to have System Engineering experience in multi-disciplinary products ( Software and Hardware). Knowledge and experience in development processes and in documentation writing is an asset in this role. Lead, design, develop, and implement test equipment and test specifications is required.Strong knowledge of one or more of the following standards such as ASTM, UL, IEC 60601-1, ISO 8536-4 and ISO 10555-1 & -5 is preferred.Knowledge of GMP and other regulatory requirement is also preferred for this position.OTHER SKILLS and ABILITIES:Test Lab Supervisor will be expected to have strong analytical reasoning with excellent communication skills.Test Lab Supervisor will have the knowledge, skill and ability to provide technical support to project teams.If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Scientist, Biosurgicals R&D |
| A minimum of a Bachelors degree is required, with a Masters degree or Ph.D. in Biochemistry, Molecular Biology, Cell Biology, Immunology or a related discipline is preferred. A minimum of 1 year of related experience is required. Must have the ability to independently design and execute experimental studies, analyze and interpret study results. In-depth knowledge and development experience in hemostasis and thrombosis, and materials design for blood-contacting applications is required. Must be able to effectively document data in notebooks, in oral presentations and writing reports. Proven track record of research and multi tasking in a Research & Development environment. Familiar with IP evaluations and product development is preferred. Previous experience in technology evaluations: an understanding of general biotechnology principles are preferred. Awareness and understanding of advanced bioanalytical techniques and test method development and validation processes are preferred. If you want to explore the many small company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today. |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Staff Scientist - Analytical Chemistry |
| A minimum of a Ph.D. in Polymer Science, Polymer Chemistry, or Material Science/Engineering with 5+ years of related experience, or equivalent, is an asset. Experience with materials used in the medical device industry is an asset. Experience in new product development processes is preferred. A background in polymer chemistry, processes and bulk polymer characterization techniques thereof (Thermal Analyses, Microscopy, Spectroscopy, Chromatography) is required. Must be able to combine characterization methods and/or adapt new methods in order to solve problems. A working knowledge of surface science processes and techniques is an asset. Good communication and presentation skills must be evident; patents, peer review publications and presentations is a plus. Must be able to communicate detailed polymer characterization data to a diverse group of technical and non-technical associates involved in the product development process. Strong interpersonal and leadership skills are essential. Ability to work in team environment, be further mentored by senior scientific fellows, and mentor junior staff members is necessary. This position is located in Somerville, NJ. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Indianapolis |
IN |
11/19/2009
|
| Indianapolis: Professional Sales Specialist II: LifeScan, Inc. |
| This position requires a 4 year degree, as well as, a minimum of 2 years of outside sales experience preferred. 3-5 years of sales experience in a healthcare professional sales environment or experience in professional diabetes care or related healthcare fields strongly preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. This position may require overnight and/or weekend travel. Excellent written and oral communication skills are essential. Preference will be given to candidates living within 30 miles of the territory, with documented history of proven sales success in outside sales, pharmaceutical, or medical products industry. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Associate III (Clinical Research) |
| A minimum of a Bachelors degree is preferred; high school graduation plus some additional training/education is required. Previous experience working in a doctor's office or hospital setting preferred. Experience working as a site coordinator, highly desirable! Must possess excellent written and verbal communication skills. Ability to analyze and organize information and data. Working knowledge of Microsoft Office, including Word, Access, Excel and Outlook. Ability to use internet to perform basic research. No travel is required. |
| Johnson & Johnson Family of Companies |
Branchburg |
NJ |
11/19/2009
|
| MANAGER, DATA MANAGEMENT - Bridgewater, NJ |
| A minimum of a Bachelor's Degree or higher in a Scientific or Medical field is required. A minimum of 6 or more years experience in Clinical Data Management is required (8 or more years experience is strongly preferred). The candidate should have demonstrated data management expertise including EDC development and experience in managing data management tasks across multiple clinical trials. Experience with project management is a plus. The candidate must have the ability to develop and maintain excellent working relationships with regulatory, clinical personnel, and external data management suppliers. Excellent written, oral, communication and organizational skills. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Senior Quality Engineer |
| A minimum of a Bachelor's degree in Engineering, Life Science, Physical Science or a related field is required, with an Advanced degree is preferred. A minimum of 4+ years of Quality Engineering experience is required. Experience in the medical device, pharmaceutical or other highly regulated industry is required. New product development experience is required. Supplier quality engineering experience is a plus. Experience with the development of Electro-mechanical devices is an asset. Knowledge of IEC 60601-1 is preferred. Knowledge of ISO and/or cGMP regulations is required. Strong knowledge in Quality Systems Regulations (QSR) preferred. ASQ certifications (CQE, CQM, CRE or CQA) is preferred. Six Sigma Green Belt or Black Belt is desired. Knowledge in Statistics, Sampling Planning, Reliability, Computer System Validation and Process Validation is an asset. Candidate must be able to communicate effectively at all levels within Quality as well as cross functionally with departments such as R&D, Operations, Purchasing, Marketing and Medical Affairs. This position may require up to 20% travel. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
San Angelo |
TX |
11/19/2009
|
| Controls/Computer Integrated Manufacturing Engineer |
| A minimum of a Bachelors degree in a Computer Science/Engineering, Electrical Engineering, or Computer Integrated Manufacturing discipline with at least two years of programming or design experience is required. Required skills include demonstrated ability to contribute in a team environment supporting 24x7 production operations and continuous improvement programs from a technical improvement standpoint. The ability to supervise personnel would be an asset. In addition, the ability to manage and report project budgets and schedules is a must. Fluency with process/operating specifications and engineering processes and practices is required. Fluency with GMPs, regulations, project management tools (MS Project) would be desired. Knowledge of spreadsheets, word processing and associated software is required. Knowledge of MS Access would be preferred. The candidate should posses a strong work ethic, be self-motivated and able to work with little supervision. Technical competences should include: Object oriented programming is required preferably in .Net framework (VB and/or C#) or VB6 Development environment. Visual Studio 2005/2008 would be preferred, Database experience in Oracle or MS SQL Server highly desired. HMI/ operator interface development - FIX32, IFIX, or RSView preferred. Web programming - ASP/ASP.net, HTML preferred. Basic knowledge with Windows 2000, XP, and/or Vista required. This position will be based in San Angelo, TX. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| Supervisor, Operations - 3rd Shift |
| A minimum of a High School diploma is required. Bachelor's degree preferred. A minimum of 3 years of experience in Logistics, Operations or a related field is required. A minimum of 2 years of experience managing people, including conducting and delivering performance appraisals is also required. Experience in inventory management, including managing cycle counts, maintaining inventory records and performing inventory adjustments are preferred. Experience using Warehouse Management Systems (i.e. MARC Global) is preferred. Knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook) is required. Experience with Ariba Procurement System is preferred. Experience with Materials Resource Planning (MRP) Systems is preferred. Experience applying Six Sigma/Process Excellence Tools, Training and/or Certification preferred. Experience working in an Automated Distribution Center environment is preferred. An APICS certification is preferred. Knowledge of Service Level Agreement (SLA) requirements is preferred. Prior experience working in a real-time/fast-paced environment required. Must have strong leadership, interpersonal, analytical and organizational skills. Must have excellent collaboration, customer service and oral/written communication skills. Experience partnering with all levels of management in a cross-functional team environment is required. Must be able to work 3rd shift (11:00 pm - 7:30 am). The ability to work in a refrigerated environment at 2 to 8 C (35 to 46 F) for 2 hours or more at a time and in a freezer at -30 to -20 C (-4 to -22 F) for up to 1 hour at a time is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Staff Quality Engineer - Irwindale, CA |
| A minimum of a Bachelor's degree in Engineering, Physical, Biological, or natural sciences, along with a minimum of 8+ years of quality, manufacturing, or research and development experience in a medical device or other regulated industry is required. An MBA, Master's, or advanced degree in an applicable field of study is an asset. An American Society for Quality (ASQ) certification is an asset. Experience or knowledge of Six Sigma, Lean Manufacturing, or Process Excellence tools is desirable. Must have the ability to use broad knowledge of regulatory, technical, and business requirements to conduct due diligence assessments. Project management experience or skills ensuring fulfillment of new product development requirements is required. Development and implementation of Quality standards applicable to the medical device or other highly regulated industry required. Knowledge of Quality and Operations systems and processes, including GMP, in a regulated industry is required. A knowledge of Quality Systems Regulations (QSR) requirements as they relate to medical devices is required. Auditing experience is an asset. Knowledge of Quality Engineering, design control, and verification and validation (V&V) tools and methodologies required. The ability to effectively communicate with internal and external personnel at all levels of the organization will be needed. Well-developed influencing and negotiation skills and the ability to effectively train and mentor a diverse array of employees at all levels of the organization will be needed. Business and financial acumen an asset. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! Due to technical upgrades, this requisition is replacing requisition # 0903032. Any candidates who have already applied to requisition # 0903032 are already being considered, therefore, you do not need to apply. |
| Johnson & Johnson Family of Companies |
Charlotte |
NC |
11/19/2009
|
| Georgia/North Carolina/South Carolina: Regional Product Marketing Manager: Ortho-Clinical Diagnostics, Inc. |
| To be considered for this role, candidates must possess: A minimum of a Bachelors degree is required. A minimum of five years of medical diagnostic industry experience including sales, product management, and/or technical experience is preferred. Excellent communication, presentation and writing skills are required. Demonstration of leadership and organization/planning skills are very desirable. Experience in infectious disease diagnostics is strongly preferred.A valid driver's license issued in one of the 50 States paired with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Newark |
NJ |
11/19/2009
|
| Newark, NJ: Regional Transfusion Medicine Manager: Ortho-Clinical Diagnostics, Inc. |
| To be considered for this position, candidates must possess: A BS/BA degree in scientific, business discipline, or equivalent experience required. MBA a plus. Diagnostic field sales experience with an emphasis on Blood Bank system and technology selling preferred. Advanced knowledge of customer blood banking processes, along with a working knowledge of the appropriate OCD blood banking products (ID-MTS gel and Provue automation) a plus. Clinical experience or related activities a plus. Knowledge of Microsoft Word, Excel, PowerPoint and Outlook required. A valid driver's license and clean driving record required. Ability to travel as necessary or required, which will include overnight and/or weekend travel. Excellent written, and oral communication skills required, with strong presentation skills preferred. Self directed and self motivated, with a proven track record of career success. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Rochester |
NY |
11/19/2009
|
| Program Manager |
| A minimum of a BS or higher degree in Biochemistry, Chemistry, Bioengineering or related field is required. Five years or more years of relevant technical experience with two or more years in a cross functional leadership role. Cross-functional technical or project leadership experience utilizing a phase-gate process to deliver new products into a regulated industry is required. Knowledge of project management tools and processes including facility with Microsoft Project is an asset. Experience with product project portfolio management is an asset. Design for Six Sigma experience is an asset. Experience in medical diagnostics or device industry is an asset. Experience with technical leadership of assay/reagent development is preferred and knowledge of Quality System Regulation, ISO, FDA and other regulatory requirements for medical device or diagnostic products is strongly preferred. Project Management Professional certification and/or MBA degree would be an asset. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Minneapolis |
MN |
11/19/2009
|
| Lab Specialist (Minneapolis Area) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. This position will based in Minneapolis, MN Area. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Tupelo |
MS |
11/19/2009
|
| Lab Specialist (Tupelo, MS) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. This position will be based in the Tupelo, MS Area. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| LAB SPECIALIST, MEMPHIS, TN AREA |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Dallas |
TX |
11/19/2009
|
| Lab Specialist (Western Texas) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Salt Lake City |
UT |
11/19/2009
|
| Salt Lake City, UT: Full Line Sales Representative: Ethicon Endo-Surgery, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as an Associate Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Boston |
MA |
11/19/2009
|
| Lab Specialist (Boston South/Providence, RI) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position.This position will be based in the Boston South/Providence, RI area. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Taunton |
MA |
11/19/2009
|
| Manager, Clinical Research |
| Minimum of a Bachelors degree in Science or related Health Field is required in this role with a Masters Degree in Science/related Health Field preferred. Also preferred is an, MBA. 10 years industry experience with 7 years experience in the Pharmaceutical or Medical Device industries is required. Strong leadership skills and the ability to develop successful strategies while fully understanding the complex environment of the assigned program. Experience in multiple functional areas strongly preferred (Clinical, Marketing, R&D, Sales)Significant project management experience with cross-functional, cross-company and international project teams. Clinical trial experience is strongly preferred and international trial experience is a plus.Strong ability to communicate clinical information (concepts and results) in oral and written communication to experts (e.g., KOL, FDA reviewers) and to product development team members (e.g., clinicians, marketing personnel, engineers)Understanding of the contribution of scientific and medical affairs goals to company business strategiesExperience drafting or reviewing technical documents (e.g., Clinical protocols/reports, design FMEAs, IOVVs). Appropriate knowledge of GMP, GCP and regulations required.Proven insight into the integration of science, regulatory, and business principles as it pertains to the successful development of multi-center clinical studies.Understanding of reimbursement landscape in the US and OUS is beneficial.Prior experience in strategic roles, along with excellent written and oral communication skills, and experience presenting to senior management also required.Ability to foster a strong collaborative team environmentDemonstrated ability to collaborate and work effectively in a fast-paced matrix environmentDemonstrated negotiation and conflict resolutions skills, including the ability to influence without clear reporting authorityStrong professional diplomacy Strong organizational skills (e.g., able to manage multiple institutions and/or projects). If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Washington |
DC |
11/19/2009
|
| LAB SPECIALIST (WASHINGTON, DC AREA) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position.This position will be based in the Washington, DC area. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Charleston |
WV |
11/19/2009
|
| LAB SPECIALIST (WEST VIRGINIA) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. This position will be based in West Virginia. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Warsaw |
IN |
11/19/2009
|
| Quality Engineer II |
| A minimum of a Bachelors Degree, preferably in a technical discipline, or a minimum of 2+ years of Engineering or Quality experience related to this role is required. A minimum of 2+ years experience within a regulated environment is required, or 1+ year experience in a regulated environment with an advanced degree. Experience in an FDA regulated environment is an asset. Process Excellence, ASQ, Lean Manufacturing training and/or certifications are an asset. Process validation and verification activity experience is an asset. Risk analysis techniques, including FMEA (Failure Modes and Effects Analysis) or other methods, is required. Problem solving techniques including root cause analysis and cause and effect analysis are an asset. Statistical techniques and methods are an asset. Blue print reading and interpretation including Geometric Dimensioning and Tolerancing (GD&T) is an asset. Must have strong negotiation skills and the ability to apply good manufacturing/laboratory practices (GMP and GLP). Working knowledge of QSR and ISO 13485 (ISO9001/EN46001) quality system requirements are an asset. Prior project management experience would be preferred. Working knowledge of Microsoft Word and Excel are required, with Access, Project, and PowerPoint knowledge an asset. Excellent written and oral communication skills will be required. The ability to work independently and partner with a cross-functional team is required. The qualified candidate for this hands-on position should be able to use Quality Engineering principles, tools, and practices to develop and optimize systems and processes that are aligned with the overall business and quality vision. Will require the ability to lift up to 25 pounds. This position will require 10-20% travel. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! Due to technical upgrades, this requisition is replacing requisition # 0901213. Any candidates who have already applied to requisition # 0901213 are already being considered, therefore, you do not need to apply. |
| Johnson & Johnson Family of Companies |
Las Vegas |
NV |
11/19/2009
|
| Lab Specialist Northern Arizona (Flagstaff, AZ or Las Vegas, NV locations) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position.This position will be based in the Northern Arizona area (Flagstaff, AZ or Las Vegas, NV locations). If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! . If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Sacramento |
CA |
11/19/2009
|
| Lab Specialist (Northern California) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position.This position will be based in Northern California. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Clinical Research Associate II (in-house) |
| A minimum of 3 years related CRA experience at medical device or pharmaceutical company required. A minimum of a Bachelors degree is required, preferably in a related field. CRA certification is preferred. Must possess excellent written and verbal skills. Must possess working knowledge of medical terminology and clinical research applications. Ability to interact and work with other departmental personnel and work as a contributing team member. Must be detail-oriented with strong organizational skills. Must have strong basic understanding of research methodology and FDA regulations. Must be able to work independently. Must be innovative, creative and flexible and able to effectively identify and resolve problems. Familiar with MS Office, including Word, Access, Excel and Outlook. Ability to use internet to perform basic research. 40-50% travel is required. |
| Johnson & Johnson Family of Companies |
Raynham |
MA |
11/19/2009
|
| Disposable Products Group Lead (2nd Shift) |
| Minimum of a High school Degree or equivalent required. Minimum 5 years of business experience preferably in Production, Operations, Procurement, Manufacturing, Supply Chain and/or related discipline. Previous experience working in a regulated environment required. This is a second shift position and requires the ability to work second shift (3:30 PM to midnight). This position requires the ability to work overtime (third shift) and weekends as needed. This position is located in Raynham, MA and does not provide relocation assistance or transportation assistance. Ability to read and write English required. Demonstrated leadership qualities required. Ability to effectively communicate and work with all Operators and Production Support Associates required. Proven track record of success is required. Ability to continuously monitor and meet daily quality standards, production metrics and efficiencies while complying with QSR, ISO and Safety regulations is required. Ability to interpret & follow detailed process specifications with no supervision is required. Ability to work in an open work area and in a clean room environment on a daily basis is required. Ability to work well independently and on small or large teams is required. Intermediate to expert level proficiency in Microsoft Office (Outlook, Excel and Word) required. Ability to lift 25 pounds and to stand and sit for extended periods of time is required. Ability to prioritize and coordinate multiple tasks and projects in an environment of competing priorities is required. Previous experience working with MRP or ERP system preferred. Experience managing workflow processes and daily production schedules strongly preferred. Experience working in Medical Device, Disposables and/or Clean Room environment is highly preferred. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Fort Washington |
PA |
11/19/2009
|
| Associate Director, Clinical Studies |
| A Doctoral degree in psychology, public health, outcomes research, or related scientific discipline is required. A minimum of 4 years of clinical and/or outcomes research experience including claims, clinician-rating, self-report, and/or biometric measures is required. Expertise in behavioral approaches/therapies within wellness and prevention is preferred. Hands-on statistical analysis skills using SPSS and/or SAS, including multivariate modeling is preferred. Excellent written and oral communication skills are required. Experience with publication record including data-based publications, poster and/or podium presentations at scientific conferences is required. Evidence of strong innovation skills preferred. |
| Johnson & Johnson Family of Companies |
Rochester |
NY |
11/19/2009
|
| ENGINEER II |
| A minimum of a Bachelors degree in Engineering or an equivalent scientific discipline is required. A minimum of 2+ years of related engineering experience is required. An Advanced degree in a relevant discipline and 3+ years of related engineering experience is preferred. Basic understanding of engineering fundamentals is required. Experience in a highly regulated industry is required. Experience in the medical device or pharmaceutical industry is an asset. Knowledge of FDA, cGMP is an asset. Knowledge of PLC, vision (camera), SCADA and HMI systems is required. Experience in manufacturing and quality systems or related applications (OTIS, QERTS, SAP) is strongly preferred. Experience with Six Sigma/Process Excellence Tools, Training, and/or Certification is preferred. Proficiency with Microsoft Project is preferred. Excellent verbal and written communication skills are required. Strong analytical/problem solving skills are a must. The ability to work on cross functional teams is required. This position will be based in Rochester, NY in manufacturing operations. |
| Johnson & Johnson Family of Companies |
St. Louis |
MO |
11/19/2009
|
| St. Louis, MO: Clinical Sales Representative - Ethicon, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least two years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Operating room medical device sales experience is preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Spokane |
WA |
11/19/2009
|
| LAB SPECIALIST- Spokane, Washington Area |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is strongly preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 70% travel will be required for this position. This position will based in Spokane, Washington Area. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Ann Arbor |
MI |
11/19/2009
|
| Ann Arbor, MI : Full-Line Sales Representative-Core: Ethicon Endo-Surgery, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Albany |
NY |
11/19/2009
|
| Albany, NY - Full Line Sales Rep - Ethicon-Endo Surgery |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Irwindale |
CA |
11/19/2009
|
| ENGINEER II |
| BS in Mechanical/Materials Engineering with minimum of 4 years of Medical Device Experience or MS in Mechanical/ Materials Engineering with minimum of 2 years of Medical Device Experience.Demonstrated proficiency with solid modeling tools, such as Solidworks and other engineering analysis tools.Experience with design of catheters, Sheaths, and/or related accessories are required.Must have at least one example of completing product development life cycle on any disposable medical deviceMust have a strong background of creating Engineering Drawings using Autocad.Must have demonstrated innovation through Patents/Publications or any other technical Reports.Experience with Extrusion, Plastic Part Design, Machining and Molding is a plus.Experience with minimally invasive surgical or catheter based devices is a plus If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Raynham |
MA |
11/19/2009
|
| Document Management Supervisor |
| Minimum of a Bachelor Degree with 4 years of experience in Quality Systems and Electronic ERP, Document and Change Management Systems in a regulated industry OR an Associate Degree with 8 years of experience in Quality Systems and Electronic ERP, Document and Change Management Systems in a regulated industry required. Supervisory experience required. Experience working with MS Office (Outlook, Word and Excel) required. Ability and willingness to assess and learn to use new tools and technologies to accomplish work are required. Ability to identify and apply quality and compliance regulations, standards, and requirements as they apply to Document Management is required. Excellent organizational skills required. Must be conscientious and attentive to detail, balanced with big-picture thinking. Must be resilient, adaptable and deal effectively with change. Strong verbal/written communications skills are required. Strong time management skills, including the ability to multi-task and prioritize work in a dynamic environment are required. Must work efficiently under pressure in order to meet demanding deadlines. Must be able to demonstrate a capacity to influence by expressing and promoting ideas, taking a clear stand on issues and making oneself understood and respected. Must be comfortable with ambiguity and uncertainty. Strong team-building skills, with the ability to function as a team player or leader on cross-functional teams is required. Ability to set tactical direction to support strategic initiatives required. Experience working in medical device industry is preferred. Experience managing transformational change and authoring and maintaining procedures and work instructions is preferred. Experience working with SAP ERP systems is preferred. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Skillman |
NJ |
11/19/2009
|
| MARKETING RESEARCH SUMMER INTERN |
| An applicant for this position should be a candidate for an MBA or MS in a Marketing Research program, with a strong academic record. The qualified candidate must be enrolled in an MBA or other business-related graduate program and planning to obtain your degree in or before July 2011. Other key qualities for success in these positions includes: The ability to think strategically and creatively. Exceptional communication and interpersonal skills. Results oriented with willingness to take responsibility and initiative. Excellent analytical skills and the ability to unbundle issues. The ability to be a team player. We have internship opportunities in Fort Washington, PA and Skillman, NJ locations. The candidate must be willing and able to intern in one of those locations. |
| Johnson & Johnson Family of Companies |
Los Angeles |
CA |
11/19/2009
|
| 2010 MBA Marketing Summer Intern, CA |
| Graduate student pursuing a MBA or Master's degree (concentration in Brand Management or Marketing is preferred). You must be enrolled in an MBA or other business-related graduate program and planning to obtain your degree in or before July 2011. Candidate must possess excellent creative instincts and strong leadership skills. Candidate must have permanent work authorization in the U.S. Candidate must be willing to work in the Los Angeles, CA location. |
| Johnson & Johnson Family of Companies |
Skillman |
NJ |
11/19/2009
|
| 2010 MBA Marketing Summer Intern, NJ |
| Graduate student pursuing a MBA or Master's degree (concentration in Brand Management or Marketing is preferred). You must be enrolled in an MBA or other business-related graduate program and planning to obtain your degree in or before July 2011. Candidate must possess excellent creative instincts and strong leadership skills. Candidate must have permanent work authorization in the U.S. Candidate must be willing to work in one of the following locations: Skillman NJ or Morris Plains, NJ. |
| Johnson & Johnson Family of Companies |
Fort Washington |
PA |
11/19/2009
|
| 2010 MBA Marketing Summer Intern, PA |
| Graduate student pursuing a MBA or Master's degree (concentration in Brand Management or Marketing is preferred). You must be enrolled in an MBA or other business-related graduate program and planning to obtain your degree in or before July 2011. Candidate must possess excellent creative instincts and strong leadership skills. Candidate must have permanent work authorization in the U.S. Candidate must be willing to in Fort Washington, PA. |
| Johnson & Johnson Family of Companies |
Irwindale |
CA |
11/19/2009
|
| Senior Complaints Analyst |
| A minimum of a Bachelor's degree in an Engineering, Life Sciences, Scientific, Nursing, or related discipline is required. A minimum of 5+ years experience in a highly regulated industry is required, with experience in an FDA (Food & Drug Administration) regulated environment required. Experience in an ISO (International Organization for Standardization) environment preferred. Knowledge of GP (Good Practices) requirements from manual to electronic processes and HIPPA (Healthcare Information Patient Privacy Act) is preferred. Proficiency with Microsoft Office, specifically with Microsoft Excel is required. Experience with Statistical Software packages (Minitab or other) is preferred. Complaint management/input system experience such as Seibel, Oracle, or a similar system is a plus. Knowledge of Medical Device, MDR (Medical Device Reporting), MDV (Medical Device Vigilance), and/or worldwide reporting is preferred. Experience working on CAPAs is an asset. Familiarity with tracking and trending processes is considered an asset. Outstanding written and verbal skills, as well as great interpersonal skills are required. An individual with strong Leadership Skills, experience with Project Management, and who is investigative and analytical is strongly preferred. This position will require 10% travel and will be based in Irwindale, CA. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Los Angeles |
CA |
11/19/2009
|
| Product Director - Retin-A Micro |
| A BA/BS degree is required. An MBA is strongly preferred. A minimum of five years of progressive marketing and/or sales experience in the healthcare industry is required. Previous forecasting and profit and loss management responsibility is required. Product management experience is required. Knowledge of dermatology market is preferred. This position requires up to 30% Domestic Travel. |
| Johnson & Johnson Family of Companies |
Miami |
FL |
11/19/2009
|
| Miami, FL: Territory Manager: Mentor Corporation, Unit of Ethicon, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of 2 years of medical device sales experience is preferred. Operating Room sales is also a plus. Skills in relationship selling, with strong customer service and interpersonal abilities. Experience selling to surgeons and operating room environment is preferred. Must work independently and take initiative. Must be able to work with minimal supervision and have strong results orientation. Plastic surgery experience is preferred. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
MA |
11/19/2009
|
| CLINICAL ACCOUNT SPECIALIST- Hartford, CT |
| Bachelor's Degree (or equivalent), RN, PA-C, CNP is required. MBA preferred. 2 years of experience working (i.e., sales, clinical, management, etc.) in an Operating Room and/or Catheter Lab environment is required. Candidates must have a valid driver's license issued in one of the 50 States and a clean driving record. Ability to travel up to 30% is necessary, which may include overnight and/or weekend travel. Candidates must have excellent written and oral communication skills as well as the ability to excel within a results and performance driven environment with a balanced base and variable compensation package. Ability to wear protective lead in the lab is required. Experience in the cardiology/cardiovascular medical device industry, preferably with EP experience is preferred. Candidates with documented leadership awards and achievements are also preferred. Prior management development classes are a plus. Preference will be given to candidates living within 30 miles of the posted geography. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
New York |
NY |
11/19/2009
|
| New York, NY: Clinical Sales Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least two years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Operating room medical device sales experience is preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today |
| Johnson & Johnson Family of Companies |
Irving |
TX |
11/19/2009
|
| Senior Polymer Engineer |
| A minimum of a Master's or advanced degree in a scientific, engineering, or related discipline is required, with a PhD preferred. A minimum of 5+ years of experience in polymer chemistry or a related discipline is required. Knowledge of product design in relation to Medical Device Directives, ISO13485 and 21CFR820 regulations and standards is required, with knowledge of QSR, Canadian Medical Device Regulations, and Japanese Medical Device Regulations an asset. Hands-on experimentalist background with experience in polymer characterization and silicone chemistry is an asset. Understanding of material characterization, structure-property, and utilization towards intended application is an asset. Experience in medical device product development is required. Experience in medical device process development and regulatory process is an asset. Knowledge of Design/Process Excellence (Six Sigma, Lean, etc.) is an asset. Knowledge of Biostatistics, FEA, and Solidworks is an asset. A demonstrated ability to work independently and in team-oriented environments, embracing change, risk, and flexibility will be needed. Must be capable of handling multiple projects/tasks at the same time as well as the ability to listen to customers' needs and develop solutions to meet their requirements. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Diamond Bar |
CA |
11/19/2009
|
| Project Manager, Regulatory Affairs (Diamond Bar, CA) |
| A minimum of a Bachelor's degree in Engineering, Physical or Biological science is required. An MS/Advanced degree is preferred. A minimum of 5+ years experience in the medical industry (Medical Device or Pharmaceutical) is required. A minimum of 5+ years experience in Regulatory Affairs or Quality Assurance of Medical Devices is required. Previous experience with global regulations and regulating agencies is required. Experience developing 510K submissions is required. Experience developing PMA submissions for class III medical devices is highly preferred. Prior experience developing IDE submissions is preferred. Experience conducting submission negotiations with the FDA, including pre-submission identification of requirements and strategy and post submission negotiations is required. Previous experience in labeling and promotional material review is a plus. This position will require 10-15% international and domestic travel. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Santa Barbara |
CA |
11/19/2009
|
| Associate Director, Business Analytics (Mentor Corporation Santa Barbara, California) |
| BS or BA required. Concentration business, marketing, finance, statistics, mathematics, or related field preferred. Advanced degree or MBA preferred. A minimum of 8 years of progressive experience in forecasting, business analytics, finance, market research, portfolio analysis, or a related field is required. Experience in the medical device, hospital specialty, or healthcare field is preferred. A minimum of 3 years experience managing people required. Proficiency in Microsoft EXCEL, PowerPoint, Crystal Ball, or Risk is required. Excellent leadership, collaboration, communication and analytical skills are required. Must be able to influence and impact others through building and defending arguments and reaching consensus of opinion. Excellent verbal and written presentation skills are required. Must be able to understand and translate data into actionable insights to support decision-making. Must be results-driven with ability to lead a team and create a productive environment for employees to consistently maintain high performing standards. Strong listening and project planning skills are required. Experience in creating market models and revenue forecasts is required. Deep knowledge of qualitative and quantitative marketing research methodologies and related statistics required. Working knowledge of industry primary, secondary data and competitive intelligence data is strongly preferred. Demonstrated success in creative problem solving and team partnership is required. This position is based in Santa Barbara and requires 30% travel as needed. |
| Johnson & Johnson Family of Companies |
Irving |
TX |
11/19/2009
|
| Maintenance Mechanic (1 of 2) |
| A minimum of a High School diploma is required. Trade school degree preferred. A minimum of 5 years of HVAC, Plumbing and/or Electrical experience is required. Experience as a Maintenance Mechanic in a commercial environment (i.e. manufacturing, industrial) is required. Prior experience in a GMP (Good Manufacturing Practice) or other regulated environment is preferred. Universal EPA certification for refrigerant recovery is required. Experience with CMMS (Computer Maintenance Management Systems) is required. Experience with MP2 is preferred. Basic electrical skills required. Basic computer knowledge is required. Must have excellent communication and practical problem-solving skills. Must have the ability to follow SOPs (Standard Operating Procedures). Knowledge of local and national building codes preferred. The ability to lift and/or move up to 50 pounds is required. Must be a team player and be able to work with minimal technical supervision. Must be able to work a staggered day shift (7:00 a.m. - 3:30 p.m., 11:00 a.m. - 7:30 p.m.), with weekend work and some overtime, requiring rotating on-call duties for any emergencies or alarms during off hours. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Santa Barbara, CA: Inside Sales Representative: Mentor Corporation |
| To be considered for this role, candidates must meet the following criteria: Bachelor's degree from a four-year college or university, and one to two years related experience preferred. Inside sales experience within the aesthetics or medical device industry strongly preferred. Knowledge of clinical, surgical techniques and procedures, and medical terminology. Skills in demonstrating a professional phone manner. Must work independently and plan extensively to meet goals. Ability to maintain accuracy, consistency and quality in a fast-paced, multitask environment. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Garden City |
NY |
11/19/2009
|
| Long Island, NY: Account Manager - Ortho-Clinical Diagnostic |
| At Johnson & Johnson we are responsible to our employees, the men and women who work with us throughout the world. Everyone must be considered as an individual. We must respect their dignity and recognize their merit. To be considered for this role, candidates must meet the following criteria: A minimum if a Bachelor's degree. A BA/BS in business or health science is preferred. A minimum of 2 years of outside business to business sales experience is preferred. Valid drivers license and clean driving record is required. Ability to travel as necessary or required, which may include overnight and/or weekend travel. Excellent written and oral communication skills is required. Prior capital equipment sales experience is a plus. If you want to explore the many small-company environments behind the big-company inpact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
New York |
NY |
11/19/2009
|
| New York, NY:- Professional Sales Specialist - LifeScan, Inc. |
| This position requires a 4 year degree, as well as, a minimum of 2 years of outside sales experience preferred. 3-5 years of sales experience in a healthcare professional sales environment or experience in professional diabetes care or related healthcare fields strongly preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. This position may require overnight and/or weekend travel. Excellent written and oral communication skills are essential. Preference will be given to candidates living within 30 miles of the territory, with documented history of proven sales success in outside sales, pharmaceutical, or medical products industry. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Tool Room Technician |
| A minimum of a High school diploma, GED or equivalent required. Vocational, technical or apprenticeship training preferred. A minimum of 3 years of Millwright, HVAC, Pipefitter, Electrician and/or Machinist experience is required. Experience as a Mechanic in a commercial environment (i.e. manufacturing, industrial) is preferred. General maintenance experience preferred. Experience managing a tool crib or parts distribution preferred. Prior experience in a GMP, GLP ISO, QSR or other regulated industry is preferred. Must be a certified Forklift Operator or be willing to become certified. Must possess a current and valid driver's license. The ability to read and understand blueprints is preferred. Knowledge of Microsoft Office (Word, Excel, Outlook) preferred. Experience navigating in a Microsoft Windows environment required. Experience with Material Management software (i.e. CribMaster), Purchasing Systems (i.e. Ariba) and CMMS software (i.e. Maximo) preferred. Must have strong communication and interpersonal skills. Must be a team player and be able to work with minimal technical supervision. The ability to work occasional overtime, weekends and some holidays is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Atlanta |
GA |
11/19/2009
|
| Atlanta, GA: Account Manager: Ortho-Clinical Diagnostics, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum if a Bachelor's degree is required. A Bachelors degree in business or health science is preferred. A minimum of 3 years of outside business-to-business sales experience is preferred. Valid drivers license and clean driving record is required. Ability to travel as necessary or required, which may include overnight and/or weekend travel. Excellent written and oral communication skills are required. Prior capital equipment sales experience is a plus. If you want to explore the many small-company environments behind the big-company inpact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Athens |
GA |
11/19/2009
|
| PROCESS DEVELOPMENT CHEMIST (POST-DOC) |
| Doctoral degree (Ph.D.) in organic chemistry or related field, with 0-2 years of relevant work experience. |
| Johnson & Johnson Family of Companies |
Providence |
RI |
11/19/2009
|
| Providence, RI: Clinical Sales Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least two years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Operating room medical device sales experience is preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today |
| Johnson & Johnson Family of Companies |
Syracuse |
NY |
11/19/2009
|
| Syracuse, NY - Full Line Sales Rep - Ethicon-Endo Surgery |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Director, Medical Writing - Janssen AI, LLC |
| A minimum of a Bachelor's degree in a science or communication discipline with a minimum of 10 years medical writing experience in the clinical or laboratory setting, OR an Advanced Degree with 7 years medical writing experience in a clinical or laboratory setting preferred. Excellent leadership and management experience. Good understanding of experimental methods, research design, and statistical analysis. Ability to analyze medical data and interpret its significance within a pharmaceutical setting. Ability to interpret, analyze, and present statistical data obtained in a clinical trial. Advanced scientific, technical reading, writing and editing skills. Excellent oral communication skills. Proficient computer and word processing skills. Use of templates and experience with document management systems. Up to 5% yearly travel may be required (International as well as Domestic). If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Head of Biometrics (Senior Director) - Janssen AI, LLC |
| A Ph.D. degree in Biostatistics or closely related field is required. A minimum of 15 years of pharmaceutical experience with at least 5 years of management level experience. International experience is strongly desired. Excellent verbal and written communication skills. Must have a working knowledge of filing regulatory documents and complex statistical methods that apply to all phases of clinical trials. Strong attention to detail and accuracy is a must. Ability to effectively present information to senior management, regulatory authorities, public groups, and other departments. Demonstrated ability to integrate planning efforts across departments to ensure organizational effectiveness. Ability to cultivate internal and external relationships based on trust and respect in anticipation of future working relationships. Demonstrated ability to proactively maximize relationships to enable successful collaboration. Demonstrated ability to facilitate a beneficial resolution of conflict. Ability to articulate a clear vision and help others understand their relationship between their roles, the roles of others and the overall goals of the organization; ability to articulate the reason behind organizational changes and demonstrate flexibility, energy and resilience throughout change efforts. Demonstrated ability to work cooperatively within and outside the organization to accomplish the best outcomes; ability to work in diverse teams to optimize decision-making. Demonstrated ability to provide coaching and feedback to foster professional development while also supporting business goals. 10-15% International and Domestic travel is required. |
| Johnson & Johnson Family of Companies |
Philadelphia |
PA |
11/19/2009
|
| State College, PA:- Professional Sales Specialist - LifeScan, Inc. |
| This position requires a 4 year degree, as well as, a minimum of 2 years of outside sales experience preferred. 3-5 years of sales experience in a healthcare professional sales environment or experience in professional diabetes care or related healthcare fields strongly preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. This position may require overnight and/or weekend travel. Excellent written and oral communication skills are essential. Preference will be given to candidates living within 30 miles of the territory, with documented history of proven sales success in outside sales, pharmaceutical, or medical products industry. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Global Marketing Director Bapineuzemab - Janssen AI, LLC |
| A minimum of a BA/BS is required with an advanced degree preferred. 10 or more years of progressive marketing experience is required, preferably in the pharmaceutical or devices industry. Extensive line marketing experience (prefer strong US experience in an infusion/biological setting), senior brand responsibility, product launch experience, and team leadership is also required. Ideally will have demonstrated success in establishing new markets/new paradigms. Minimum of 2 years strategic global marketing leadership experience. Line marketing experience demonstrating commitment to innovation through deep customer insights is key. Demonstrated track record leading highly matrixed, cross-functional work teams composed of high-level managers and executives. Experience with global R&D programs required. Extensive experience accomplishing objectives through people. Position requires significant domestic and some international travel (approximately 50%). |
| Johnson & Johnson Family of Companies |
Garden City |
NY |
11/19/2009
|
| Long Island, NY: Breast Care Specialist: Ethicon Endo-Surgery, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Baltimore |
MD |
11/19/2009
|
| Baltimore, MD: Breast Care Specialist: Ethicon Endo-Surgery, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Tampa |
FL |
11/19/2009
|
| Tampa, FL- Clinical Sales Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least two years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Operating room medical device sales experience is preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today |
| Johnson & Johnson Family of Companies |
White Plains |
NY |
11/19/2009
|
| Westchester, NY- Full Line Sales Rep - Ethicon-Endo Surgery |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Central Islip |
NY |
11/19/2009
|
| Clinical Account Specialist Long Island, NY |
| Bachelor's Degree (or equivalent), RN, PA-C, CNP is required. MBA preferred. 2 years of experience working (i.e., sales, clinical, management, etc.) in an Operating Room and/or Catheter Lab environment is required. Candidates must have a valid driver's license issued in one of the 50 States and a clean driving record. Ability to travel up to 30% is necessary, which may include overnight and/or weekend travel. Candidates must have excellent written and oral communication skills as well as the ability to excel within a results and performance driven environment with a balanced base and variable compensation package. Ability to wear protective lead in the lab is required. Experience in the cardiology/cardiovascular medical device industry, preferably with EP experience is preferred. Candidates with documented leadership awards and achievements are also preferred. Prior management development classes are a plus. Preference will be given to candidates living within 30 miles of the posted geography. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Jacksonville |
FL |
11/19/2009
|
| SENIOR RESEARCH OPTOMETRIST |
| A minimum of a Bachelors Degree in Optometry, Doctoral Degree in Optometry, PhD in Vision Sciences or MD with specialty in Ophthalmology is required. Post-graduate degree or residency in cornea and contact lenses preferred. A minimum of one year working experience in clinical research of contact lens products or vision science is preferred. It is required for the candidate to have patient care experience. General knowledge, understanding and application of principles, concepts and practices of clinical research are preferred. Working efficiently under pressure, ability to manage multiple projects simultaneously is required. Strong organizational, communication and analytical skills is required. Familiarity with Optics and Wavefront aberrations are preferred. MS/PhD in Physiological Optics is preferred. |
| Johnson & Johnson Family of Companies |
Portland |
ME |
11/19/2009
|
| Portland, ME- Full Line Sales Rep - Ethicon-Endo Surgery |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Associate Director, Regulatory Affairs (Santa Barbara, CA) |
| A minimum of a BA/BS degree and RAC certification are required; an advanced degree is strongly preferred. A minimum of 5 years experience in a senior Regulatory Affairs and/or CMC role within Biotech and/or Pharmaceuticals is required. Regulatory Project Management experience is required. Experience in biologics is required. Experience in preparing BLAs in eCDT format is required. Strong knowledge of regulatory requirements (21 CFR Parts 312, 600, 601, 610 and 820) and CMC experience are required. Experience selecting and managing outside vendors is required. Experience processing electronic submissions is required. Global experience is preferred. Travel approximately 25%, but can go up to 80% during peak times with regular travel to manufacturing facility in Madison, WI. PMP certification is preferred. |
| Johnson & Johnson Family of Companies |
San Antonio |
TX |
11/19/2009
|
| San Antonio, Texas - Territory Assistant: Ethicon Products, Unit of Ethicon, Inc. |
| Qualified candidates will have a minimum of a Bachelors Degree coupled with at least 2 years of solid Business to Business sales with demonstrated results. Candidates should have experience in product sales to a highly educated/high profile customer base. Candidates with Medical Device, Surgical or Capital equipment experience are preferred. Must be willing to work in an Operating Room environment. Candidates must have a valid driver's license and clean driving record (no more than 2 moving violations and/or accidents within a 6 month period and no more that 3 in a 3 year period). A current method of effectively targeting accounts and achieving results through a daily action plan. Important: This job requires the candidate to be willing to relocate and/or travel at any given time based on the needs of the company within the geographical sales region. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Springfield |
MA |
11/19/2009
|
| Worcester, MA: Energy Sales Specialist - Ethicon-Endo Surgery |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Raynham |
MA |
11/19/2009
|
| Supplier Quality Engineer I |
| A minimum of a Bachelor's degree is required, preferably in an Engineering, Life Science, or a related discipline. This position will require a minimum of 0-2+ years experience (including internships, co-ops, or other related experience). A Masters/Advanced degree is an asset. Other experience that is an asset, but not required, will include: Experience in a highly regulated industry is an asset. Experience in the Medical Device industry is preferred. Experience in the Pharmaceutical industry is an asset. FDA and ISO regulations knowledge is an asset. Auditing knowledge is an asset. Strong communication, teamwork, and problem solving skills will be needed. Knowledge in root cause analysis skills are an asset. Experience or knowledge with machining manufacturing processes and injection molding an asset. Six Sigma, Lean, or ASQ Certification and trainings an asset. This position will require up to 20% travel. |
| Johnson & Johnson Family of Companies |
Columbia |
SC |
11/19/2009
|
| Columbia, SC: Breast Care Specialist: Ethicon Endo-Surgery, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
San Antonio |
TX |
11/19/2009
|
| San Antonio, TX: Associate Sales Representative: Ethicon Endo-Surgery, Inc. |
| To be considered for this role, a Bachelor's degree is required. The ability to travel as necessary, depending on geography (potentially overnight and/or weekends) and willingness to relocate nationally within the first year of employment is required. Two years of outside selling experience is preferred. Candidates must have a valid driver's license in one of the 50 states and clean driving record, as well as excellent written and oral communication skills. Candidate's must either be in active military service or within 12 months of active service or within 12 months of receiving their college degree. Candidates with documented successful sales performance (high growth, results vs. plan), the ability to target accounts and achieve results through a daily action plan and the ability to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributor reps) and KOLs, is preferred. Self-starters with strong time management and planning skills are also a plus. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| Maintenance Technician III |
| A minimum of a High School diploma, GED or equivalent degree required. Associate's degree in a technical discipline preferred. Technical school courses and/or previous factory training in Conveyer Systems or building mechanical/electrical/HVAC systems maintenance preferred. A minimum of 5 years of Conveyor Systems maintenance experience required. Experience in the following areas preferred: Programmable Logic Controllers (PLCs), rolling stock (forklift), building mechanical/electrical/HVAC systems. Prior experience in a FDA regulated industry preferred. Packaging machine maintenance experience preferred. Knowledge of maintenance programs and documentation preferred. The ability to work with tools (i.e. hand tools, power tools, etc.) is required. Experience operating a forklift and willingness to become certified as a Forklift Operator required. Must have the ability to follow policies, Standard Operating Procedures (SOPs) and complete work tasks accurately and efficiently. Must have excellent verbal communication skills and demonstrated collaboration skills with team members and management. The ability to lift at least 50 pounds on a repetitive basis, stand and/or walk on concrete floors 90% of the time and bend, twist and perform repetitive tasks are required. The ability to work from heights (i.e. ladders, platforms, and lifts) and under low clearance equipment required. Must be able to work 3rd shift and be available to work other shifts (1st or 2nd). The ability to work overtime, weekends and holidays as needed by business is required. Must be available for rotating on-call duties. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Raynham |
MA |
11/19/2009
|
| Polish Operator I |
| A minimum of a High school diploma, G.E.D. or equivalent required. A minimum of 1 year of experience working in a machine shop or production line environment, machining precise finished products is required. Experience working in a Medical Device manufacturing environment preferred. Experience working in a Good Manufacturing Practice (GMP) or other regulated environment preferred. Experience working in an environment that has gone through Lean process changes preferred. The ability to be flexible to change and support change during a Lean process transformation is required. Grinding or buffing experience preferred. Basic mechanical skills required. Experience with routine machine inspection preferred. Experience with measuring devices preferred. Knowledge of blueprint reading and geometric tolerance dimensions preferred. Basic computer skills required. The ability to work independently and in a team environment is required. Ability to communicate effectively (read, write, and speak) in English is required. Basic math skills, with the ability to add, subtract, multiply, divide, compute percentages and work with decimals required. The ability to perform and record measurements with drop indicators, venires and gauges is required. The ability to stand and/or walk more than 50% of the time is required. Ability to lift up to 25 pounds unaided is required. Must be able to work 3rd Shift (9:30 PM - 6:00 AM, Sunday through Thursday). The ability to work occasional overtime and holidays is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Providence |
RI |
11/19/2009
|
| Providence, RI: Hernia Sales Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: Excellent written and oral communication skills, a Bachelor's degree, valid driver's license issued in one of the 50 States and clean driving record, 3+ years experience in field sales, preferably medical device and/or capital equipment. Operating room/surgical sales experience strongly preferred. Documented successful sales performance (high growth, results vs. plan). Experience in product sales to a highly educated / high profile customer base. Ability to target accounts and achieve results through a daily action plan. Ability to travel as necessary or required, which may include overnight and/or weekend travel. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Denver |
CO |
11/19/2009
|
| Denver, CO - Alternate Care Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today. |
| Johnson & Johnson Family of Companies |
Omaha |
NE |
11/19/2009
|
| Omaha, Nebraska - Hernia Sales Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: Excellent written and oral communication skills, a Bachelor's degree, valid driver's license issued in one of the 50 States and clean driving record, 3+ years experience in field sales, preferably medical device and/or capital equipment. Operating room/surgical sales experience strongly preferred. Documented successful sales performance (high growth, results vs. plan). Experience in product sales to a highly educated / high profile customer base. Ability to target accounts and achieve results through a daily action plan. Ability to travel as necessary or required, which may include overnight and/or weekend travel. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Charlotte |
NC |
11/19/2009
|
| Charlotte, NC - Alternate Care Sales Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Kansas City |
MO |
11/19/2009
|
| Kansas City, MO: Full-Line Sales Representative-Core: Ethicon Endo-Surgery, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Houston |
TX |
11/19/2009
|
| Houston, TX: Alternate Care Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is preferred required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today. |
| Johnson & Johnson Family of Companies |
Seattle |
WA |
11/19/2009
|
| Seattle, WA: Alternate Care Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is preferred required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today. |
| Johnson & Johnson Family of Companies |
Chicago |
IL |
11/19/2009
|
| Chicago, IL - Alternate Care Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today. |
| Johnson & Johnson Family of Companies |
Tampa |
FL |
11/19/2009
|
| Tampa, FL: Alternate Care Sales Representative: Ethicon Products, Unit of Ethicon Inc |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Miami |
FL |
11/19/2009
|
| Miami, FL: Alternate Care Sales Representative: Ethicon Products, Unit of Ethicon Inc |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Ann Arbor |
MI |
11/19/2009
|
| Ann Arbor, MI : Clinical Sales Representative: Ethicon Products, Unit of Ethicon, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least two years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Operating room medical device sales experience is preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Raleigh |
NC |
11/19/2009
|
| Senior Quality Assurance Engineer |
| A minimum of a Bachelor's degree in Engineering, Science, Technology or a related discipline is required, with a minimum of 5+ years experience in a highly regulated industry required, with experience in the medical device or pharmaceutical industry preferred. A minimum of 3+ years experience as a Quality Engineer is required. CQE or equivalent certification is an asset. Experience with Chemical Processing, Chemistry, or in a related lab area is an asset. Thorough understanding of FDA Quality System Regulation, MDD, ISO 13485:2003, quality engineering methodology, and quality management principles are an asset. Working knowledge of Standards applicable to Medical Device Industry are an asset. Experience with medical device product design and manufacturing processes is an asset. Knowledge of statistical tools and techniques is an asset. Experience in analytical problem solving is an asset. Proven accomplishment in Quality System Auditing is an asset. FDA Notified Body experience as a team member is an asset. Personal computer and software applications experience, including e-mail, Internet applications, Word processing, spreadsheet, and database work is required. Statistical Analysis program, Minitab, or other statistics software experience is required. Must be able to work within a team and handle multiple tasks. Experience with dimensional tools (e.g. rulers, optical comparators, calipers, micrometers, pin gauges) and balances/scales is an asset. This position is located in Raleigh, NC. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Birmingham |
AL |
11/19/2009
|
| Birmingham, AL: Core Sales Representative: Ethicon Endo-Surgery, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as an Associate Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Philadelphia |
PA |
11/19/2009
|
| Philadelphia, PA: Alternate Care Sales Representative: Ethicon Products, Unit of Ethicon Inc |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Boston |
MA |
11/19/2009
|
| Boston, MA: Alternate Care Sales Representative: Ethicon Products, Unit of Ethicon Inc |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Phoenix |
AZ |
11/19/2009
|
| Phoenix, AZ: Alternate Care Sales Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Albuquerque |
NM |
11/19/2009
|
| Spring Semester Co-op, Ethicon Endo Surgery (ABQ) |
| In order to be eligible for a 2010 Fall R&D Co-op position, candidate must be enrolled in an accredited college/institution and be in good academic standing pursuing a Bachelors or Masters degree in Mechanical Engineering, Biomedical Engineering or related field. Only students in their Sophomore year or above will be considered. A minimum GPA of 3.0 is strongly preferred, with demonstrated leadership/participation in campus programs and/or community service activities. Students must be available to work during session indicated and must be authorized to work in the United States and not require sponsorship in the future. To learn more about Ethicon Endo-Surgery, please visit our website at www.ethiconendo.com. |
| Johnson & Johnson Family of Companies |
Skillman |
NJ |
11/19/2009
|
| Associate Scientist, Preclinical Studies (BetaLogics) |
| M.S. or B.S. with a minimum of 2 years relevant experience in scientific discipline is required. Must show basic understanding of laboratory techniques associated with work assignments. Schedule experiments in the lab and perform research in a timely, competent manner. Able to independently solve routine problems and develop solutions. Recommend modifications to methodology and understand the impact of those modifications on the broader research area. Able to review, analyze, and interpret data, especially as requires in-depth evaluation of various factors of increasing and/or changing complexity. Prepare technical reports, summaries, written protocols, and analysis. Interact with employees inside and outside of the immediate working group in a collegial, professional manner, sharing information and expertise. Foster communication and collaborative teamwork. Provide guidance to new or junior personnel. May serve as liaison to wider internal or external scientific community. Knowledge of GLP is an asset. |
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| Memphis, TN: Professional Sales Specialist, Lifescan Inc. |
| A minimum of a 4 year degree is required. Two years of outside sales experience is preferred. 3 years of sales experience in a healthcare professional sales environment or experience in professional diabetes care or related healthcare fields strongly is preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. This position may require overnight and/or weekend travel. Excellent written and oral communication skills are essential. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Chicago |
IL |
11/19/2009
|
| Chicago West, IL : Territory Manager: Mentor Corporation, Unit of Ethicon, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of 2 years of medical device sales experience is preferred. Operating Room sales is also a plus. Skills in relationship selling, with strong customer service and interpersonal abilities. Experience selling to surgeons and operating room environment is preferred. Must work independently and take initiative. Must be able to work with minimal supervision and have strong results orientation. Plastic surgery experience is preferred. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Manager, Clinical Data Management - Janssen AI, LLC (1 of 2) |
| High School diploma required. Med Tech background preferred. BS/BA degree preferred. A background in Life Sciences is a plus. A minimum of 5+ years of data management experience within a pharmaceutical and/or health care environment required. Electronic data capture experience preferred. Experience managing external vendors is required. Knowledge of FDA regulatory requirements is strongly preferred. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Senior Clinical Budget Analyst - Janssen AI, LLC |
| A Bachelor's Degree is required. Working knowledge of the clinical development process and 2+ years of experience in clinical budget development and management are required. Must possess an understanding of clinical trials, regulatory affairs, quality assurance, clinical trial materials, budgeting and routine contracts. Previous experience with industry benchmarking database(s) is strongly preferred. Excellent communication skills (both oral and written) are required. The ability to work effectively in cross-functional teams is required. Strong and proven negotiation and problem resolution skills are also required. Strong business acumen and an innovative spirit are required. Strong inter-personal and collaboration skills are required. Must possess the ability to accomplish substantial tasks with minimal supervision. Experience in assisting and drafting of legal contracts and familiarity of clinical budget development and negotiation is required. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Senior Clinical Contract Analyst - Janssen AI, LLC |
| A Bachelor's Degree is required. A certificate of completion of formal course in Paralegal studies is preferred. Certification of Notary Public is a plus. Working knowledge of the clinical development process and 2+ years of experience in clinical budget development and management are required. Must possess an understanding of clinical trials, regulatory affairs, quality assurance, clinical trial materials, budgeting and routine contracts. Excellent communication skills (both oral and written) are required. The ability to work effectively in cross-functional teams is required. Strong business acumen and an innovative spirit are required. Strong inter-personal and collaboration skills are required. Must possess the ability to accomplish substantial tasks with minimal supervision. Familiarity of clinical budget development and/or negotiation is required. |
| Johnson & Johnson Family of Companies |
Cincinnati |
OH |
11/19/2009
|
| STAFF DESIGN ENGINEER - ELECTRICAL |
| BS degree in electrical engineering, or related field is required. MS degree is preferred. At least 8 years of experience in the planning, design, and commercialization of electrical or electro-mechanical systems, including embedded software is required. The ideal candidate will have a demonstrated track record of driving technically appropriate solutions and the effective use of new technology. DFSS or similar certifications preferred. Medical products or other highly regulated industry is an asset. Technical leadership and project management, particularly with globally outsourced projects is an asset. RF Analog products with experience in design, test and interconnecting/cabling is a requirement for this role. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
San Francisco |
CA |
11/19/2009
|
| San Francisco/Sacramento, CA: Alternate Care Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is preferred required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today. |
| Johnson & Johnson Family of Companies |
San Francisco |
CA |
11/19/2009
|
| Senior Database Administrator (Contract) |
| A minimum of 3 years of experience as MySQL DBA on Unix/Linux on MySQL 4.1 and/or 5.0. Excellent knowledge and experience in InnoDB & MyISAM is required. Experience in DB backup, recovery, replication, High Availability is required. Experience as an Oracle DBA (RMAN, standby server) is nice to have. Excellent skills in SQL and scripting languages (Perl/Python/Unix Shells, etc.) is desired. Nagios or Cacti monitoring work is a plus. This role will require 24/7 pager rotation. |
| Johnson & Johnson Family of Companies |
Los Angeles |
CA |
11/19/2009
|
| Associate Director, Statistical Programming (Cougar Biotechnology) |
| BS degree in statistics, biostatistics, mathematics, computer science, or other relevant scientific areas is required; a MS or PhD degree in relevant areas is preferred. A minimum of 10 years of SAS programming experience with 5 or more years of clinical trials experience is required. This position requires 8-10 years of experience in the pharmaceutical/biotech industry. Ability to work with cross-functional teams a must. Good oral communication skills required. Prior experience managing a group is required. Prior work experience in the oncology area is preferred. Additionally, it is preferred that the candidate have excellent programming skills in SAS and/or S+ and other related tools; applied knowledge and understanding of clinical development programs and industry trends such as e-submission process and CDISC; and basic knowledge of software development life cycle, 21CFR Part 11, and other FDA regulations. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Global Commercial Leader - Janssen AI, LLC |
| Bachelor's degree required; advanced degree preferred. A minimum of 14 years of progressive marketing experience preferably in the pharmaceutical or devices industry; extensive line marketing experience (prefer strong US experience in an infusion/biological setting), senior brand responsibility, product launch experience, and team leadership required. Ideally will have demonstrated success in establishing new markets/new paradigms. A minimum of 2 years strategic global marketing leadership experience required. Demonstrated track record leading highly matrixed, cross-functional work teams composed of high-level managers and executives. Experience with global R&D programs preferred. Extensive experience accomplishing objectives through people. Position requires significant domestic and some international travel. |
| Johnson & Johnson Family of Companies |
Irving |
TX |
11/19/2009
|
| Lean Manufacturing Engineer |
| A minimum of a Bachelor's degree in Mechanical, Industrial, Electrical or Chemical Engineering required. A Master's degree preferred. A minimum of 3 years experience of process improvement experience required. Black Belt Certification required. PMP Certification preferred. Advanced computer skills and use of software applications such as iGrafx or similar software is required. Must have excellent analytical and statistical skills. Knowledge of Lean Manufacturing principles, including: Value Stream Mapping, Kaizen, One-Piece Flow, Kanban, Cellular Manufacturing, Six Sigma, Set-up Reduction, Visual Management, required. Must have proven initiative, creativity, assertiveness and leadership abilities. Must be able to work under pressure, achieving consistently high results through individual and team efforts. Must have excellent interpersonal, influencing, communication, presentation, listening, negotiating and problem-solving/decision-making skills. Must have the ability to set priorities and achieve objectives. Project management and cost/benefit analysis experience required. Capacity Planning experience, including productivity measurements, manpower planning and material flow, is required. Must have the ability to read, analyze and interpret common scientific, technical journals and financial reports. Must have the ability to write reports with technical emphasis. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Senior Manager, Internal Communications |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Mgr, Clinical Operations (Process Management & Training) |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr Mgr, Clinical Operations (Process Management & Training) |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr Software Engineer, Cognos Reporting |
|
| Millennium Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Clinical Program Manager |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Associate Director, CMC Regulatory |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Associate Director/Director, Molecular Medicine |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr. Manager, Regulatory CMC |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Scientist I/Scientist II, Molecular Technologies |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| MGR II, REGULATORY AFFAIRS |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Associate Director, Regulatory CMC |
|
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Scientist I, Chemical Engineer |
| - A Ph.D. degree with 1+ years of pharmaceutical industry experience; an MS degree with 3+ years of pharmaceutical industry experience; or a BS degree with 6+ years of pharmaceutical industry experience. Degrees with a life science concentration required, with a preference for concentrations in chemical engineering or chemistry.
- A demonstrated understanding and working knowledge of chemistry and chemical engineering fundamentals; advanced technical knowledge and experience in API process development, process scale-up, troubleshooting, and optimization; applied kinetics, thermodynamics, and transport fundamentals; as well as familiarity with modern laboratory instrumentation (HPLC, GC, FTIR, Raman, FBRM, DSC, TGA, XRPD, etc), automation tools, and laboratory/plant implementation of PAT
- Experience with modeling complex, physicochemical systems; data analysis; statistical design of experiments; QbD concepts, and fluency with common physical property and process modeling tools (Aspen, Dynochem, Matlab, etc.)
- A track record of successful laboratory and pilot-scale development in the areas of reaction engineering, catalysis, crystallization, separation technologies, drying, and micronization
- The ability to successfully interact, lead, and collaborate within an interdisciplinary team environment comprised of organic, physical, and analytical chemists; project team members; and manufacturing personnel
- Experience with the management of external scientific activities and CRO/CMO relationships
- Proven communication (verbal and written) and interpersonal skills
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Associate Director, Analytical Development |
| - A Ph.D. in the life sciences with a preference for a concentration in analytical chemistry
- 8+ years of current, related and practical experience in the pharmaceutical industry
- Experience with HPLC, GC, spectroscopy, and GMP
- 5+ years experience direct management and supervisory experience
- Excellent leadership, teamwork and organizational skills
- Excellent verbal and written communication skills
- The ability to collaborate effectively with other scientists in a multidisciplinary project team environment
- Past success while working in a fast-paced, goal-oriented, team environment
- Innovative and detail oriented, exhibiting a sound scientific approach to data interpretation and experimental design
- Established scientific credentials with strong theoretical understanding of analytical chemistry and the pharmaceutical development process
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr Scientist, Chemical Development |
| - A Ph.D. degree with 6+ years of current and relevant academic, post-doctoral, or industrial process chemistry experience; an MS degree with 7+ years of industrial process chemistry experience; or a BS degree with 10+ years of industrial process chemistry experience. Degrees should have a life science focus with a preference for a concentration in Chemistry, Organic Chemistry, Process Chemistry or Medicinal Chemistry
- The proven ability to successfully interact, lead, and collaborate within an interdisciplinary team environment comprised of organic, physical, and analytical chemists; chemical engineers, project team members; and manufacturing personnel
- A track record of innovation, self-starting and success working in a multi-disciplinary team under defined timelines
- Experience operating under GMP guidelines with a preference for a working knowledge of quality principals
- Working knowledge of NMR and HPLC
- Experience interacting with contract research (CRO) and contract manufacturing (CMO) organizations
- The ability to communicate ideas across an organization through effective verbal and written communication skills
Although Vertex does not have an active opening, we are interested in establishing relationships with well qualified and talented individuals for future opportunities in our Chemical Development group in Cambridge, MA.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company?s strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex?s product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Scientist II, Analytical Development |
| - A Ph.D., Master's, or Bachelor's degree in the life sciences or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry
- 3+ years (PhD), 5+ years (MS) or 8+ years (BS) current, relative industry experience working in drug substance and drug product support
- A broad understanding of the drug development process, including clinical design, chemical development, and formulation development, especially how these processes impact analytical method development, validation, and method transfer
- Working knowledge of the risks that exist in all aspects of method development, validation and transfer and the ability to use risk analysis and quality-by-design (QbD) approaches to develop robust methods, design appropriate validation protocols to validate methods for their intended use, and ensure successful method transfer are essential
- Experience working with in ICH and FDA method validation guidelines with preference for the ability to identify areas overlooked by these guidelines
- Hands-on GMP experience with a preference for a background in developing GMP friendly methods
- Skilled in HPLC, LC-MS, GC, GC-MS, FT-IR, UV-VIS, KF, NMR, dissolution and other instruments
- The ability to work successfully in team/matrix environment as well as independently
- The ability to work in a fast pace environment, to manage priorities, and to maintain timelines for multiple projects
- Excellent written and verbal communication skills
Although Vertex does not have an active opening, we are interested in establishing relationships with well qualified and talented individuals for future opportunities in our Analytical Development group in Cambridge, MA.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company?s strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex?s product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Senior Financial Analyst |
| Minimum Requirements
-Bachelors? degree and 3+ years of experience in Financial Analysis
-Strong leadership and communication skills. This position requires frequent interactions with various levels throughout the organization.
-Solid presentation skills. Ability to present financial and nonfinancial data together effectively.
-Flexibility to adjust to changing pace and needs of the organization.
-Ability to work independently and exercise judgment.
-Ability to develop and improve financial and business processes.
-Ability to work in collaborative environment
-Proven financial leadership
Desired skills/background
-Accounting experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Senior Scientist- Solid State Method Development |
| SKILLS/ABILITIES:
? Solid state chemistry applied to pharmaceuticals
? Experimental design and statistical analysis for Analytical Chemistry
? Computer applications and proficiency
? cGMPs, ICH Guidelines and Compendial Requirements
? Project planning and management
? Oral and written communications
? Mentoring of staff
PERSONAL ATTRIBUTES:
? Motivated self starter
? Team player
? Ability to lead small scientific group
? Committed to quality
? Well organized, efficient worker
? Good interpersonal skills
? Good problem solver
? Creative, innovative thinker
? Developer of people
? Easily adaptable to change
? Brings closure to work in a timely manner
EDUCATION AND EXPERIENCE:
PhD in Chemistry or materials science in related field with 7+ years of experience, Masters Degree in Chemistry with 10+ years of experience, or Bachelors Degree in Chemistry with 12+ years of experience or equivalent.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
San Diego |
CA |
11/19/2009
|
| Temporary Scientific Associate (Analytical Development) |
| * Requires a BS degree in Chemistry and 5+ years of relevant experience or MS degree in Chemistry and 3+ years of relevant experience.
* Must have analytical chemistry experience in a pharmaceutical or related field.
* Must have experience using HPLC/GR instruments.
* Chemical Manufacturing & Control (CMC) environment experience is highly preferred.
* Highly self-motivated, you must have good communication skills both written and verbal, be able to multitask, be flexible and have the ability to work in a flexible cross-functional team environment.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Regulatory CMC Manager |
| ? Demonstrates expert knowledge of FDA regulations, guidelines, and precedents related to drug product development, including Quality by Design (QbD) initiatives
? Knowledge of EU, Canada and ROW regulations, guidelines and precedents
? Proven ability to impact team decision making
? Ability to communicate with all levels within the company and can act as liaison / representative both internally and externally
? Exhibits project management skills necessary to perform complex tasks independently and work on multiple projects simultaneously
? Has a proven track record of successful interaction with regulatory authorities and in preparation of major regulatory submissions
? M.S. (or equivalent degree) and 4+ years of relevant work experience
? B.S. (or equivalent degree) and 6+ years of relevant work experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr Scientific Associate, Analytical Development |
| - A Master's or Bachelor's degree in the life sciences or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry
- 0 - 4 years of academic experience in a chemistry or analytical chemistry laboratory setting with some previous related industry experience preferred
- Familiarity with, or a desire to gain a working understanding of, HPLC, LC-MS, GC, GC-MS, FT-IR, UV-VIS, KF and other instruments used in the analysis of pharmaceutical products
- An interest in and passion for establishing a career in analytical development and the biopharmaceutical industries
- The ability to work successfully in both a team environment as well as independently
- Excellent written and verbal communication skills
- Established organizational skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr. Systems Analyst |
| Necessary technical skills:
? Experience implementing and supporting proven middleware technologies.
? Languages: SQL, PL/SQL, scripting languages
? Databases: Oracle 10g
? OS: Unix, Linux, Windows
? ETL Tools: Data Loader, SQL*Loader
? Use of API?s in data processing following coding standards
Preferred technical skills (a plus):
? Applications: Oracle E-Business Suite11 i (11.5.10.2), specifically Oracle Process Manufacturing and Oracle supply chain modules
? Developer Tools: Oracle Developer Forms, Oracle Developer Reports, Oracle Discoverer (9i, 10g), Oracle Alerts, Oracle Workflow builder, BI Publisher (XML Publisher), Web ADI
Technical and Communication Skills:
? Ability and desire to learn quickly and in a self-paced environment
? Hands on experience with Oracle 11.5.10 HR, OPM, and Supply Chain Management
? Ability to work within a fast-paced small team to deliver quality results
? Ability to work interactively with users, management and support team.
? Team contributor with good communication skills and strong analytical, problem solving skills.
? Expertise in Oracle 11.5.10 financials modules like Oracle General Ledger, Oracle Payables, Oracle Assets, Oracle purchasing, Cash Management, Project Accounting is a plus
Preferred Education and Experience Levels:
? B.S and 5 years relevant work experience.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr. Medical Writer |
| Ph.D. (or equivalent degree) and 2 ? 5 years of relevant work experience, or M.S. (or equivalent degree) and 3 ? 6 years of relevant work experience, or B.S. (or equivalent degree) and 4 ? 8 years of relevant work experience
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Manager |
| ?Proven ability to manage teams working on complex tasks
?Proven ability to design and/or execute procedures and communicate those procedures to others
?Demonstrates an in-depth understanding of applicable regulations
?Displays ability to influence within technical area of expertise
?Proven ability to manage projects of moderate scope and complexity
?Exhibits understanding of technical disciplines beyond own specialty area
?Proactively identifies and resolves problems
?Demonstrates strong oral and written communication skills
?B.S. (or equivalent degree) and 6+ years relevant work experience
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Director, Clinical Planning and Trial Activation |
| *
Must possess demonstrated clinical planning and process improvement experience, as well as experience in strategic planning and achieving results in a growth-oriented environment
*
Ability to influence senior management and partner with various internal departments
*
Experience in demonstrating leadership, influence and collaboration in a matrix-managed environment
*
Solid management experience and the ability to hire and develop staff, as well as leverage resources from within function
*
Proficiency with the application of Project Management tools, methodologies, practices, risk analysis, decision analysis and contingency planning
*
Strong consultative, listening and analytical skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Buyer |
| Knowledge of Microsoft Office required. Experience with Oracle preferred. Bachelor's Degree preferred.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Systems Analyst-Enterprise Content Management |
| Preferred Education and Experience Levels
B.S and 5 years relevant work experience.
Knowledge/Skills Needed:
? Experience working in IT in regulated environments
? Must have excellent technical troubleshooting skills
? Good system analysis, design skills and familiar with SDLC methodology, particularly IQ, OQ, PQ
Technical
? Experience in ECM technologies such as Trackwise, QUMAS DocCompliance and Documentum (Content Server, eRoom)
? Experience in portal technology development and standards (JSR168, WSRP)
? Object-Oriented design skills: Java, JDK 1.4.x J2EE (JSP's, Servlet's, Tag Libraries) XML, XML Schema.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Director, National Accounts |
| - A Bachelor's degree with a preference for an MBA or PharmD
- 10 + years experience in pharmaceutical and/or biotechnology industries
- 4 + years of National Account experience, including experience managing large accounts as well as major pharmacies, medical, actuarial, and case management organizations
- 4 + years of direct management experience with a preference for experience managing a field based manage care organization
- In-depth knowledge of current trends in regulation and reimbursement modalities as well as managed care and payor landscapes
- Highly successful and demonstrated experience implementing pull-through programs
- Ability to multi-task as well as be strategic, creative and innovative in a dynamic, fast paced matrix team environment
- Ability to complete projects and achieve goals on time while delivering high quality results
- Possess strong initiative and ability to identify issues and create solutions
- Outstanding customer relationship, interpersonal and communication skills with the established ability to effectively communicate across diverse audiences and influence cross functionally
- Strong analytical skills with the proven ability to effectively analyze data sets to determine trends and establish strategies
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| QA Associate, Quality Systems |
| A B.S. in a scientific or allied health field (or equivalent) and 0 ? 3 years of relevant work experience in the Biotech or Pharmaceutical industry
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Temp QA Specialist |
| Bachelor's degree or equivalent in the Sciences. 5-7 years experience.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Clinical Data Manager |
| Bachelor?s degree in related science/technical discipline
Minimum of 3-5 years data management experience in Pharmaceutical/Biotechnology industry.
Knowledge and experience with Electronic Data Capture (EDC) system and other data management systems.
Ability to juggle multiple tasks and priorities.
Analytical and problem-solving skills, with good attention to detail.
Excellent communication skills (oral and written) and interpersonal skills.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Regulatory Project Manager |
| PREFERRED EDUCATION AND EXPERIENCE:
BS or BA is required. A minimum of 5 years experience in an FDA-regulated industry is required including a minimum of 3 years project management experience.
Vertex Pharmaceuticals |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate/Senior Research Associate: Target validation and Protein Expression |
| The position requires a BS or MS in Biology or a related field with a minimum 2 years of practical experience in a research laboratory. Industry or academic experience and previous work in biochemical, cancer, immunological, cell culture and molecular biology techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate/Senior Research Associate: Target function ? MAb assays - Agensys, Santa Monica, CA |
| The position requires a BS or MS in Biology or a related field with a minimum 3 years of practical experience in a research laboratory in the required activities. Industry experience and previous work in biochemical, immunological, cell culture and cell-based techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Translational Research - Agensys, Santa Monica, CA |
| Candidate consideration requires a BS/MS in molecular and cellular biology or similar field with a minimum of 3 years of relevant laboratory experience. Industrial experience in Oncology drug discovery is preferred. Successful candidates will have strong written and oral communication skills and be self-motivated. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Target Validation and Protein Expression, Agensys - Santa Monica, CA |
| The position requires a BS or MS in Biology or a related field with a minimum 2 years of practical experience in a research laboratory. Industry or academic experience and previous work in biochemical, cancer, immunological, cell culture and molecular biology techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Target Validation and Protein Expression, Agensys - Santa Monica, CA |
| The position requires a BS or MS in Biology or a related field with a minimum 2 years of practical experience in a research laboratory. Industry or academic experience and previous work in biochemical, cancer, immunological, cell culture and molecular biology techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate ? Antibody Production, Hybridoma, Agensys - Santa Monica, CA |
| ?X BSc or MSc in Cellular Biology, Biology, Bioprocess Engineering or related field. ?X Minimum of 2 years relevant experience. ?X Extensive mammalian tissue culture experience, preferably gained in an antibody production environment. ?X Knowledge of antibody production from hybridoma or recombinant cells. ?X Excellent verbal and written communication.?X Excellent organizational skills.Additional skills (useful but not essential):?X Experience with wave form bioreactors?X Experience with stirred tank bioreactors |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Medical Director, Medical Science - Oncology |
| M.D. degree, Board Certified or Board Eligible in Designated SpecialtyMinimum three years clinical experienceMinimum two years laboratory or clinical research experience and five years experience in the pharmaceutical industry or equivalent academic experience.Strong working-knowledge of regulatory procedures and guidelines (preferably US)Effective team player in a matrixed R&D environmentAble to work independently on all aspects of assigned projectsExcellent presentation and writing skillsExcellent organizational skills |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Medical Affairs Director, Latin America |
| REQUIREMENTS:- A minimum of five (5) years in a Medical Director Role.- Medical Degree; must have a License of Medical Doctor & Board certification in at least one specialty with basic medical science and research experience. - Strong people management skills- Basic marketing skills as well as understanding business practices and technical terms in business. - Business acumen, a bottom-line orientation, strong management and leadership skills. - Must have proficiency in both Spanish and English (Portuguese a plus) in order to interact with the other team clinicians at the corporate headquarters in the US, as well worldwide. - Present, discuss, negotiate & persuade the global team in English- Self motivated, both strategic and tactical in his/her thought process and capable of becoming rapidly engaged in the company?s business- High degree of self-direction, with the ability to quickly make decisions and accept responsibility for outcomes |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Director, Regulatory Affairs- Agensys, Santa Monica, CA |
| Bachelor?s degree in life sciences, Chemistry, Biology preferred. Advanced degree is a plus. 8-10 years previous biotechnology and/or pharmaceutical drug development experience. Scientific knowledge in chemistry, general biological/physical science and ability to apply that knowledge to regulatory issues and product development. Recognized as an expert in regulatory strategy and submissions. A minimum of 5 years regulatory affairs experience preferably involving direct contact with the FDA; full knowledge of FDA & ICH regulations and guidelines, and the ability to provide interpretations of that information to others. Proven record of successful IND/NDA submission and negotiations with the FDA. Strong organizational skills with the ability to manage large projects and provide regulatory guidance/training to others in the department as needed. Proven ability to prioritize and multi-task with minimal supervision based on interactions with project team members. Excellent written and oral communication skills, with writing ability to meet regulatory requirements and standards. Ability to communicate effectively and maintain effective working relationships. Must be able to positively influence direct Agensys staff and colleagues and groups within Astellas global organization. Highest integrity with respect to professional standards and maintenance of proprietary, confidential information. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Associate Director, Pharmacovigilance QA Lead |
| 1. Minimum B.A/B.S. in science (biology, chemistry, pharmacy) or relevant related field of study. 2. Minimum of 5-to-9 years experience in pharmaceutical or biotechnology industries, including safety quality assurance and management experience 3. Ability to work independently and also within teams are essential4. Ability to travel up to 20% domestically and/or internationally 5. Working knowledge of FDA and international regulations (e.g., Volume 9a) 6. Ability to interact and communicate effectively with various levels of management. 7. Excellent communication and project management skills 8. Computer skills to include Microsoft Office (Power Point, Visio, Excel), Access and Project 9. Excellent facilitation, negotiation, problem-solving, and conflict resolution skills 10. Initiates and maintains extensive contacts within both internal and external networks 11. Excellent oral and written communication skills including the ability to present formally and informally within area of expertise to a diverse set of audiences, including senior management and external customers |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Senior Director, Quality Assurance |
| 1. Minimum BA / BS or equivalent, advanced degree preferred, with 15 years of industry experience, 10 years of QA experience, and minimum of 6 years managing staff.2. Comprehensive knowledge of GxP and other regulations for pharmaceuticals and biologics and understanding of global quality standards and regulatory authority inspection trends relating to product development, submission and commercialization. Demonstrated knowledge and experience with quality oversight of global clinical trials and pharmacovigilance operations. Demonstrated ability to establish local and regional Quality policies and to influence the development and implementation of global Quality policies in support of the quality system.3. Effective written and oral communication and interpersonal skills, facilitation, negotiation and influencing skills with an demonstrated ability to drive, champion and negotiate organizational support for strategic initiatives, projects or programs, both internally and externally within Astellas group and with external stakeholders. Plays a key role in the identification and implementation of long-term business planning strategies, assuring quality is taken into consideration.4. Demonstrated ability to provide leadership for key strategic issues and significant QA policies, practices and processes with respect to quality compliance with minimal executive management oversight. 5. Demonstrated experience in making decisions to resolve the most complex problems and in providing sound compliance advice and direction in a manner that has a significant impact across the Astellas Group and external stakeholders.6. Demonstrated ability to anticipate, proactively respond to trends, and/or shifts in the external environment (e.g., regulatory, business partner relationships, industry standards) and to predict impact to quality assurance and/or Astellas business.7. Track record of effective management and development of quality assurance professionals. Demonstrated ability to both lead and manage the Quality Assurance department, comprised of multiple functional quality assurance units. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Manager/Sr Manager, Market Research |
| REQUIREMENTS:- Bachelor?s degree is required, Master?s degree preferred.- Must have a minimum of 3-6years successful experience in the pharmaceutical or other related healthcare field in the area of market research and analysis. Strong, proven experience in qualitative and quantitative methodologies is required.- Extensive computer proficiency with desktop software in a Windows environment required: Microsoft Word; Microsoft Excel; Power Point required. - Excellent skills are required in the following areas: organization, written and verbal communication, accuracy and personal initiative.- Experience in forecasting, market model development is a strong positive.- Supervisory experience is a plus |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Senior Director, IT Account Management and Shared Services |
| ? Advanced Degree or equivalent experience required.? Ten plus years related experience required. Pharma industry preferred.? Extensive knowledge and skill through broad and/or deep experiences in IT. ? Strong communication and interpersonal skills, capable of motivating and influencing teams.? Perform at the highest levels and able to make decisions independently.? Able to translate between technical and business leaders at the highest levels.? Viewed as credible, and well respected by the business and IT organizations.? Accountability in building and maintaining positive and cooperative working relationships. ? Collaboration and cross functional facilitation skills.? Demonstrated understanding of project management, quality assurance, and IT best practices.? Proficiency with commercial applications that are designed to support enterprise wide business capabilities. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Clinical Studies, Manager |
| B.S./B.S.N., RN, M.S. in life sciences or Pharm D. with at least five years clinical trials management or equivalent experience. Must have excellent interpersonal skills, written and verbal communication skills, administrative skills and computer ability as well as working knowledge of protocols, clinical drug development process and clinical study design and planning. Must have sufficient therapeutic area and drug knowledge to support internal and external presentations. Requires proven time management and project management skills. Must also have proven leadership ability, knowledge of FDA/GCP/ICH requirements and familiarity with the pharmaceutical industry. Moderate (20% - 40%) travel required.Manages clinical studies; does not supervise employees. Manages relationships internally and externally. |
| sanofi pasteur |
Swiftwater |
PA |
11/19/2009
|
| Manufacturing Tech V |
| BS Degree in a related field and 2 - 4 years experience preferred or 10 years or more equivalent work experience. Trackwise, SAP and deviation experience a plus. |
| sanofi pasteur |
Swiftwater |
PA |
11/19/2009
|
| Manager, Process Integration US |
| Bachelors Degree in a Life Science. 5-10 years Pharmaceutical/Biological laboratory experience in a GMP compliant Quality Control laboratory, including previous management experience. Proven team collaboration experience is essential with a focus on customer service. |
| sanofi pasteur |
Swiftwater |
PA |
11/19/2009
|
| Manager, Manufacturing Staff US |
| BS degree in Life Sciences or Engineering with relevant experience in manufacturing of biological products. 3-5 years experience in manufacturing and/or development departments. Working knowledge of cGMP's. Must have knowledge of continuous improvement techniques and problem solving skills. Excellent verbal and written communication skills. Working knowledge of SAP, validation and analytical experience is preferred. Candidate must be able to work overtime and flexible hours, including weekends. |
| sanofi pasteur |
Swiftwater |
PA |
11/19/2009
|
| Library & Information Access Intern |
| College science background in Biology or Chemistry or Library/Information Science.
- Minimum overall GPA of 3.2
- Full-time matriculating student who has completed sophomore year at an accredited college or university
- Demonstrated leadership skills
- Excellent communication and organization skills
- Strong proficiency with MS Office applications
- Good interpersonal skills a must
- Good attention to detail
- Database, information science or library background a plus, especially cataloging. |
| sanofi pasteur |
Swiftwater |
PA |
11/19/2009
|
| Biostatistician |
| Ph.D. in Statistics or related field or equivalent experience; 3-5 years (MS. and 5-7 years) relevant pharmaceutical/vaccines industry experience.
At least 2 years experience using SAS software, especially base, statistics, and graphics.
At least 2 years experience designing clinical trials.
At least 2 years experience developing statistical analysis plans and statistical methods sections for protocols.
Demonstrated use of sample size estimation and power calculation tools/software.
Very good oral and written communication skills.
Demonstrated ability to work independently and to work in a multidisciplinary team.
Experience with non-inferiority trials, a plus.
Author or co-author of publications, a plus.
NDA, BLA, or CTD submission experience, a plus. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Biologist |
| This position requires candidate to be currently enrolled in a BS level program in Biology, Microbiology, Virology. Successful candidates will possess superior communication and interpersonal skills. Laboratory experience is preferred. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # BIO002391. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Chemical Engineer |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001968. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Chemist |
| This position requires candidate to be currently enrolled in a BS program in Chemistry or Biochemistry. Ideal candidate will possess superior communication and interpersonal skills. Laboratory experience is preferred. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002018. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Development Program |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Mechanical Engineering, Industrial Engineering, Chemistry/ Biochemistry, Biology/ Microbiology, or Supply Chain Management. Ideal candidate will possess superior communication and interpersonal skills, a team player with the ability to work independently. Must be graduating between August 2009 and August 2010. Must be willing to be assigned to different jobs and potentially different sites over the first two years of employment. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002036. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Engineer |
| This position requires candidate to be currently enrolled in a BS program in Mechanical, Industrial, Electrical Engineering or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # ENG002103. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Merck Technical Rotation Program |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Chemistry/ Biochemistry, Biology/ Microbiology. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002035. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Staff Chemical Engineer |
| This position requires candidate to be currently enrolled in a MS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002019. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Senior Chemical Engineer |
| This position requires candidate to be currently enrolled in a PhD program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002024. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Senior Chemist |
| This position requires candidate to be currently enrolled in a PhD program in Chemistry or Biochemistry. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002034. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Chemical Engineer |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001998. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Chemical Engineer |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001988. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Chemical Engineer |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001978. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Biologist |
| This position requires candidate to be currently enrolled in a BS level program in Biology, Microbiology, Virology. Successful candidates will possess superior communication and interpersonal skills. Laboratory experience is preferred. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # BIO002401. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Manufacturing Development Program |
| This position requires candidate to be currently enrolled in a MS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Mechanical Engineering, Industrial Engineering, Chemistry/ Biochemistry, Biology/ Microbiology, or Supply Chain Management. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002049. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Manufacturing Technical Rotation |
| This position requires candidate to be currently enrolled in a PhD program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002053. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003868. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003878. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003888. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003898. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003908. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Science Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Biology, Microbiology, Virology, Chemistry or Biochemistry. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ADM003932 Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003918. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003928. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Merck Manufacturing Science Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Biology, Microbiology, Virology, Chemistry or Biochemistry. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ADM003942. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Graduate Intern |
| This position requires applicant to be currently working toward a working toward graduate degree in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Statistics or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000318. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Senior Research Chemist (Continuous Recruitment) |
| Required PhD in Chemistry or Biochemistry is required. Degree completion no later than end of 2010 required. DesiredSome relevant experience via a co-op, internship, or independent research is preferred for consideration. If you, like us, strive for excellence in all you do, consider joining our team of talented and dedicated individuals from diverse backgrounds who are united in bringing Merck's finest achievements to people around the world. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers/university/ to create a profile and submit your resume for requisition # CHE002098. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| MMD PhD Biology College Recruiting |
| · PhD Biology, Microbiology, Virology· Strong personal character and ethics· Superior Communication and Interpersonal Skills· Excellent Academic Achievement, Analytical Ability· Ability to work effectively with others as well as independently· U.S. citizen or lawful permanent resident of U.S.· Laboratory experience is preferred Opportunities exist in manufacturing areas and include opportunities in process validation and manufacturing technical areas. Opportunities are available in analytical, biological, and vaccine development. Each of these opportunities provides a challenging environment to learn and contribute. The successful candidate will be expected to carry out research on assigned problems in the above listed areas, including applied development, problem solving, process / product improvement and laboratory testing in the above listed areas. Many analytical techniques are used, including both in vivo and in vitro methods, to characterize complex biological products and systems The candidate is expected to work in a team environment and provide all essential understanding toward addressing mechanisms responsible for product safety, efficacy and stability. Responsibilities will also include the analysis and interpretation of data for problem solving and predictive purposes. A company-wide program is available to facilitate individual development planning to prepare the individual for increasing responsibility according to either technical or management tracks support career path planning. This may include movement to other divisions of Merck & Co., Inc. Those who join Merck can look for substantial early responsibility, the opportunity to develop and apply state-of-the-art technologies, chances for growth and advancement in an informal, varied work environment. Specific openings in MMD are as follows:Global Vaccines Technology and Engineering (West Point, PA, Elkton, VA) is responsible for process implementation, validation and maintenance for biological processes. Specific needs are in the Bioanalytical area which is responsible for assay development and support.At Merck we believe you can develop faster if we give you real challenges right from the onset. In MMD, we encourage you to move between functional groups so that you get hands-on experience in many aspects of our operations.If you are the kind of individual who thrives on challenge and possess the technical, leadership and business skills that are of value to our business, we invite you to apply. Please go to www.merck.com/careers and enter your profile and resume for requisition BIO002450 so that we can keep track of you through the whole recruiting process. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Chemical Engineer |
| Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002008. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Whitehouse Station |
NJ |
11/19/2009
|
| MMD MS Chemistry College Recruiting |
| QualificationsThis position requires candidate to be currently enrolled in a MS program in Chemistry or Biochemistry. Ideal candidate will possess superior communication and interpersonal skills. Laboratory experience is preferred. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002122. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating day shift (6AM-6PM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001961. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Lab Animal Vet |
| Education Requirement: DVM or VMD Required:At least 2 years post-doctoral training or experience in laboratory animal science is required along with team orientation. Must possess strong leadership and interpersonal skills. Must communicate effectively with all personnel within department and members of the Merck Research Lab Research community. Demonstrates ability to coordinate activities and careers of subordinates. Desired:Diplomate status, ACLAM is preferred or relevant specialty with an AVMA recognized veterinary specialty organization. At least 4 but no more than 8 years experience or MS/PhD in the specialty of laboratory animal care. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world.We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # LAB000108. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm Representatives Please Read Carefully:Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Process Scientist (Adjuvants) |
| The desired candidates will posses a M.S. or PhD in Chemical Engineering or Chemistry (physical and/or analytical) with 1 to 5 years experience (graduate work may count toward this experience). Proven industrial experience with modeling and characterization of aluminum-containing adjuvants in highly desired. To succeed in this role, the candidate will be highly qualified and have a clear understanding of how physical, chemical and engineering properties of processes relate to controlled formation of precipitated particles and to their structure and properties. The candidate should also be familiar with analytical techniques such as X-ray diffraction, FTIR, and/or NMR. Experience with aluminum-containing adjuvant characterization and identification techniques is considered a plus. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #BIO002469. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Specialist |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 3 years of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends, and to complete several months of training on first shift. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001974. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends, and to complete several months of training on first shift. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Manufacturing Supervisor |
| Required Education:High School or GED Preferred:B.S. with emphasis in Science or Engineering Experience RequiredMinimum 2 years working experience in cGMP or equivalent environment. Willingness to work off-shift or weekends. Computer literacy in MS Office, Word, Outlook, Excel. PreferredcGMP experience in a sterile, bulk or finished pharmaceutical environment. Supervisory experience in a heavily regulated industry (ex. FDA, Military, Nuclear, Petro-Chemical). Manufacturing plant experience in operational capacity. Experience working within a Union environment. Experience with working in SAP or other Enterprise software. Technical writing experience related to investigations in to mfg process variation. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000345. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. ZZ5ML |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Senior Manufacturing Supervisor |
| Educational Requirements:High School or GED Required Experience/Skills:Minimum 3 years of Supervisory experience. Minimum 2 years working experience in cGMP environment. Willingness to work off-shift or weekends. Computer literacy in MS Office, Word, Outlook, Excel. Preferred: Education:B.S. with emphasis in Science or Engineering. Experience:cGMP experience in a sterile, bulk or finished pharmaceutical environment. Supervisory experience in a heavily regulated industry (ex. FDA, Military, Nuclear, Petro-Chemical). Manufacturing plant experience in operational capacity. Experience working within a Union environment. Experience with working in SAP or other Enterprise software. Technical writing experience related to investigations into manufacturing process variation. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000338. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. ZZ5ML |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Staff Engineer - Fermentation Process Support |
| Required:Bachelor degree in Engineering or Science field 2 years experience in an engineering or operations position supporting a manufacturing process through one or more of the following roles: process improvements, monitoring process performance, investigating atypicals and implementing corrective actions, creating standard work for operations, and assisting in troubleshooting of the process. Preferred:Experience with technical support of a GMP (good manufacturing practices) manufacturing process BS degree in Chemical Engineering, Biotechnology, Chemistry/Biochemistry Experience in bioprocess manufacturing Experience with fermentation and/or purification processes for production of proteins Supervisory experience Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002156. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Staff Engineer |
| Education:· B.S in Engineering, Biological Sciences, Chemistry or Physics. M.S. in Engineering, Biological Sciences, Chemistry or Physics preferred.Required:· Minimum of 4 years work experience required; with 2 years of work experience specifically in the field of validation. Specific experience in at least one of the following areas is required:· Filter performance qualification using Filter Integrity testers, bubble point, and diffusive flow testing. Experience in validation desired; alternatively, experience in engineering or operations is acceptable with use of sterilizing filters, tangential flow filtration, ultra filtration, and vent filters.· Container/ Closure Integrity testing using microbial ingress and helium leak testing. Experience in validation desired; alternatively, experience in engineering or operations using welders, sealers, and aseptic fluid transfers using sterile bags and manifolds is acceptable.· Experience in a GMP or ISO13485 laboratory performing microbiology, environmental monitoring or engineering development work. Support the GVTE / BSV Lab Coordinator, with performing instrument qualification, metrology, SOP development , creating training material, lab notebook review, performance of internal audits (chemical hygiene, safety, 5S, GMP), and carrying out improvements activities and corrective actions in response to audits.Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ENG002123. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Environmental Services Manager |
| Requirements: Bachelor's required. Concentrations in an environmental discipline highly preferred. Relevant professional certifications and/or Six Sigma Green Belt a plus. Minimum 10 years applied environmental professional work experience in a pharmaceutical, chemical or manufacturing environmental, coupled with 3 years in a position of environmental program leadership. Proficient in federal and state and regulatory programs. Excellent leadership, program management, project management, and organizational skills. Excellent verbal and written communication skills. Excellent interpersonal and negotiation skills. Proficiency in MS Word, MS Excel, MS Powerpoint. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ENV000114. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Supplier QA Relationship Manager |
| Education:BS/BA degree in an Engineering, Science, or Business field. Required:Minimum 6 years experience in commercial, business, quality, technical or manufacturing operations functions. Must have strong demonstrated interpersonal and communication skills. Must have demonstrated personal networking and relationship building skills. Ability to work independently with all levels of the organization is required. Familiarity with regulatory requirements that govern GMPs (e.g. CFR and Eudralex). Travel to supplier locations to develop and manage the supplier/Merck relationships is a key enabler of success with this position. The travel expectations are ~ 10% to 25%. Experience writing SOPs, Policies, and/or Guidelines. Ability to use Microsoft Excel to enter data and use formulas to calculate information. Experience developing PowerPoint slides and delivering presentations to management. A key responsibility of this position is to serve as the primary point of contact for coordination, oversight, problem solving and communication with MMD's suppliers. Must have tangible experiences, either internal or external to Merck, associated with relationship building and networking. Preferred:Technical writing skills, and experience with data management, collection and analysis. A strong knowledge of and broad experience in Quality Assurance. Experience in conducting or participating in atypical process investigations is preferred, as working with suppliers to resolve problems and implement corrective actions using problem solving techniques is a key expectation. Experience developing process flowcharts and using Microsoft Visio. Familiarity with the MMD Quality Management Systems (QMS). Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001949. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Supplier QA Data Management Coordinator |
| Education:BS/BA degree in an Engineering, Science, or Business field. Required:Minimum 5 years experience in commercial, business, quality, technical or manufacturing operations functions. Familiarity with regulatory requirements that govern GMPs (e.g. CFR and Eudralex) Experience writing SOPs, Policies, and/or Guidelines. Ability to use Microsoft Excel to enter data and use formulas to calculate information. Experience developing PowerPoint slides and delivering presentations to management. Excellent analytical and computer skills, including software packages used in the maintenance and analysis of data. Excellent interpersonal and communications skills. Ability to work independently with all levels of the organization along with strong planning/organization skills. Preferred:Experience using Lean Six Sigma tools, particularly Black Belt or Green Belt certification. Familiarity with the MMD Quality Management Systems (QMS). Experience operating a database to enter, store, retrieve, and trend data and well as document management (e.g. MIDAS, Documentum, Panagon). Experience developing process flowcharts and using Microsoft Visio. Familiarity with Microsoft Project to assist in developing project plans and timelines. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001933. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Site Compliance Specialist |
| Education:A Bachelor of Science in a life science (such as Biology, Chemistry, etc.) or an appropriate Engineering field is required; candidates with majors in other fields will not be considered. A major in Biology, Microbiology, Biochemistry, Virology, or Engineering is preferred. Required:At least two (2) years of experience, in broad based quality control and/or quality assurance audits or inspections, or other experience in a variety of manufacturing, packaging, testing, or technical support areas. Desired:Experience in bulk vaccine manufacturing or other bulk vaccine support area is desirable. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001929. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Co-op- Viral Vaccine Engineering Services |
| This position requires applicants to be pursuing degree in Chemical, Mechanical, or related Engineering discipline. A Grade Point Average (GPA) of at least 3.0 is preferred. Candidate must be available for full time employment (40 hours per week) for a period of 6 months targeted to begin in March 2010. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities" create a profile and submit your resume for requisition #ADM004026. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Co-op Global Vaccine Technology & Engineering |
| This position requires applicants to be pursuing degree in Chemical or related Engineering discipline, with a focus on technical support or related field. A Grade Point Average (GPA) of at least 3.0 is preferred. Candidate must be available for full time employment (40 hours per week) for a period of 6 months targeted to begin in March 2010. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities" create a profile and submit your resume for requisition #ADM004028. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Bio-Process Technician |
| Education: Bachelor degree in Life Science or Engineering OR Associates degree in Life Science or Engineering and 2 years experience working in the FDA regulated industry. Required:Must be able to lift 50 lbs Must be willing to be vaccinated/blood tested for titer for products manufactured within the facility Must be flexible to work different shifts Preferred:Experience in biological and/or vaccine processing preferred Experience performing aseptic/sterile operations Experience with GMP's (Good Manufacturing Practices) Mechanical aptitude and ability to analyze equipment and take appropriate corrective action Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # PRO007545 Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Validation Manager - Formulation and Filling |
| Qualifications:Minimum of a B.S. in Engineering or Science required. M.S. or PhD. in Engineering or Science will be considered. Preferred fields of study include Chemical Engineer, Biochemical Engineer, or Biological Sciences. Minimum of 8 years with all or some of experience in a sterile validation or Quality experience required (can be obtained through a combination of post-graduate education and work-related experience). Minimum of 6 years of the above noted experience is required if MS or PhD degree has been attained Demonstrated leadership and teamwork skills, excellent analytical abilities, proven written and verbal communications skills. Experience preparing regulatory submissions and managing interactions during regulatory inspections required. Ability to gain cross-functional consensus and skilled in conflict resolution. Knowledge of PDA Technical Reports, active member of PDA or other recognized industry group, is preferred. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002102. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Release Coordinator |
| EducationA Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. RequiredAt least three (3) years of relevant post-degree work experience in a manufacturing or research environment or a related field. Strong analytical, problem solving, oral and written communication skills, leadership, and attention to detail. Solid understanding of regulatory requirements and GMPs. PreferredAseptic gowning may be required. Tites may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000134. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Release Associate |
| Required:B.S. degree with a technical emphasis in an appropriate scientific or engineering field. At least one year of relevant post-degree work experience in a laboratory, manufacturing, or quality position. Evidence of leadership skills coupled with good oral and written communication skills, i.e. effective presentation of concepts and ideas, as well as interpersonal and conflict resolution skills. Attention to detail, flexibility and an awareness of production and attendant quality control problems. Preferred:Familiarity with manufacturing batch records is a key skill necessary for success in this position; prior batch record experience is a strong plus. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000124. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Sr. Engineer/Scientist - Manufacturing Process Technical Support |
| Minimum Qualifications: Bachelor's degree in Chemical, BioChemical or Bioprocess Engineering with 5 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR Master's degree in Chemical, BioChemical or Bioprocess Engineering with 2 years experience in a GMP Biopharmaceutical manufacturing or research and development environment Preferred Qualifications:Experience providing technical support of a GMP manufacturing process, specifically in protein purification and/or fermentation. Experience writing technical documentation: such as change controls, protocols, operating procedures. Experience with commissioning, qualification, and validation of biopharmaceutical equipment and processes. Demonstrated expertise in bioprocessing unit operations such as fermentation, chromatography, tangential flow filtration Demonstrated ability to lead a group of individuals in task oriented assignments such as technical investigations, root cause analysis, equipment installation Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002082. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Process Engineer/Scientist - Pharmaceutical Manufacturing Process Support |
| Basic Qualifications: Bachelor's degree in Chemical, BioChemical or Bioprocess Engineering with 7 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR Master's degree in Chemical, BioChemical or Bioprocess Engineering with 5 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR PhD in Chemical, BioChemical or Bioprocess Engineering Preferred Qualifications:Experience leading and developing people and teams Experience and expertise in protein purification or fermentation Project management experience Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002084. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Instrumentation Technician |
| Required:High School Diploma or GED Effective calibration/troubleshooting skills Ability to communicate and work in a highly effective team environment Ability to manage multiple priorities and advance several tasks in parallel Demonstrated mechanical aptitude Operation/use of general hand and power tools, instruments and testing apparatus common to the electronic and instrumentation fields Ability to read P&ID's, electrical drawings, blueprints, PLC ladder logic, etc Asset:Experience in aseptic or GMP/regulated manufacturing environment Ability to work with and troubleshoot computer control equipment, including Programmable Logic Controllers (PLCs) and Distributed Control Systems (DCS) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # PRO007495. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Manufacturing Supervisor |
| Please note that this positon is a rotating shift position: 12 Hour Rotating Shift(2 Days on - 2 Days Off then 5 days on)Hours will be 6 AM - 6PM and/or 6PM - 6AM Qualifications (Required): Manufacturing SupervisorEducation:High School or GED Experience/Skills:Minimum 2 years working experience in cGMP or equivalent environment Willingness to work off-shift or weekends Computer literacy in MS Office, Word, Outlook, Excel Qualification (Preferred):Manufacturing Supervisor Education:B.S. with emphasis in Science or Engineering Experience cGMP experience in a sterile, bulk or finished pharmaceutical environment. Supervisory experience in a heavily regulated industry (ex. FDA, Military, Nuclear, Petro-Chemical) Manufacturing plant experience in operational capacity Experience working within a Union environment Experience with working in SAP or other Enterprise software Technical writing experience related to investigations in to mfg process variation Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000327. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. ZZ5ML |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating day shift (6AM-6PM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000131. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating day shift (6AM-6PM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000137. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000141. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000133. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Operations Coach - Cap & Inspect Production Leader |
| Required: Minimum 2 years coaching/supervisory experience. Minimum 4 years experience in a manufacturing role in an FDA regulated environment Bachelor Degree in Engineering or Science field Asset:Manufacturing experience with automated vial capping and/or inspection equipment Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000389. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Staff Biochemist |
| Education Minimum Requirement: Master's Degree or a Bachelor's degree with a minimum 2 years of industry experience Required Experience and Skills: Experience with mammalian cell culture and cell-based potency assays, both on a large scale Basic knowledge of MS Word and Excel Desired Experience and Skills: Experience with automation, ie Backman instrumentation Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # BIO002470. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Whitehouse Station |
NJ |
11/19/2009
|
| Global Payroll Lead |
| Required:A minimum of ten (10) years experience working in a business environment. A minimum of five (5) years managing a global payroll function/operation. A minimum of five (5) years managing people and vendors. Desired:A minimum of two (2) years payroll experience in 2 regions outside the US Business process improvement experience (Six Sigma preferred). Knowledge of ERP (SAP preferred). Certified Payroll Professional (CCP) designation. A minimum of 2 yrs experience working in a shared services environment. Fluency in French. Broad understanding and knowledge of HR business processes. Solid oral and written communication and interpersonal skills. Education Requirement:Bachelor's degree required, masters preferred. A concentration in HR highly desired. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # HUM001307. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Project Scientist |
| Education:BS in Biological Sciences Required. MS in Biological Sciences Preferred Required experience: 3 years post-bachelors degree experience in supply for therapeutic proteins/vaccines/biologics (may be combination of post-graduate education and/or work-related experience.) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #PRO007555. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Staff Biochemist |
| Education:BS in Biological Sciences Required. Required experience: 1 to 3 years post-bachelors degree experience in analysis and supply of biologics (may be combination of post-graduate education and/or work-related experience.) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #PRO007589. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Senior Engineer/Scientist |
| Education Requirement: BS/MS/PhD in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry with at least 6 years relevant experience (May be combination of post-graduate education and/or work-related experience.) Required: Has technical expertise in mammalian and/or yeast based systems. Has demonstrated ability for independent project leadership. Desired: Both downstream and upstream experience preferred, but in-depth experience in one area acceptable. Prior experience in late stage bulk process development, process validation, authoring regulatory BLA sections and/or working with external contract organization for development and or manufacturing would be preferred. Working understanding of analytical methods to characterize biologics, US/EU regulatory requirements is a plus; working knowledge of cGMPs is an added benefit. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # SCI003914. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Release Analyst |
| EducationA Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. RequiredAt least three (3) years of relevant post-degree work experience in a manufacturing or research environment or a related field. Strong analytical, problem solving, oral and written communication skills, leadership, and attention to detail. Solid understanding of regulatory requirements and GMPs. PreferredAseptic gowning may be required. Tites may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000149. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Manufacturing Engineer |
| Educational requirements: B.S. or M.S. in Chemical or Mechanical Engineering. Required skills and experience: The position requires basic technical writing skills and strong oral communication. Minimum 1 year Aseptic or pharmaceutical manufacturing experience, technical support or quality role or equivalent. Preferred skills and experience: Minimum 3 year Aseptic or pharmaceutical manufacturing experience, technical support or quality role or equivalent. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002179. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Operational Coach- Manufacturing Maintenance Leader |
| Required:Minimum of 6 years experience in a manufacturing maintenance role within a GMP facility. Minimum 4 years coaching/supervisory experience Bachelor degree in Engineering or Science Asset:Vaccine/sterile experience Plant maintenance, project engineering and/or operations experience Computer Maintenance Management System (Maximo) SAP Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000272. Merck is an equal opportunity employer, M/F/D/V proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Gen. Techn.-Sheet Metal Worker |
| Education: High School Diploma or equivalent required. Graduation from a recognized sheet metal trade school, OR the completion of a formal sheet metal worker apprectice program. Requirements: At least three years recent full-time experience as a journeyman sheet metal worker, OR the recent completion of four years' on the job training as part of a formal sheet metal worker apprentice program. Preferred: More than 3 years experience as a Journeyman sheet metal worker Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # USW000188. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Process Engineer |
| Education: BS in Chemical Engineering, Bio-Engineering or Biosciences. MS in Chemical Engineering, Bio-Engineering, or Biosciences preferred. Required:Demonstrated Technical Strength. Strong Analytical Problem-Solving. Ability to lead teams. Effective Communication, both verbal and written. Strong Collaboration & Leadership experience. Preferred:GMP experience, Cell Culture and/or Virology experience. Previous Technology Transfer experience. Experience with Aseptic Processing and related equipment desired. Knowledge and experience of CIP and SIP. Knowledge or experience of six sigma methodology, process analytical technology, process monitoring and control. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # PRO007596. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm Representatives Please Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Zebrafish Research Associate (BS/MS) |
| Minimum:
? B.S/B.A or M.S. degree in a biological science with a minimum 5 years laboratory research experience
? Proficiency in the use of current molecular biology techniques and cloning strategies, quantitative PCR, site-directed mutagenesis, construction of reporter systems, assessment of protein levels using antibody reagents, and the design and use of various expression vectors
? Experience using gene knockdown, over-expression or microinjection technologies, including RNA interference, to assay the function of pathway activity in.
? Excellent organizational, communication and computer skills.
Preferred:
? General knowledge of zebrafish husbandry
? 1+ years experience in a zebrafish laboratory
? Experience working with a model organism: embryology, genetics and developmental biology principles, whole mount gene expression analysis, phenotypic analysis.
? Familiar with microscopy and imaging. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Wnt Scientific Associate, Developmental & Molecular Pathways |
| B.S. or M.S. in Biochemistry, Cell Biology or Molecular Biology
Minimum 5 years experience in biochemistry, mammalian cell biology working with various cell lines and/or cell signaling mechanisms
Previous experience with stable cell line production, design and analysis of cell-based assays, transfection and viral transduction technologies and genetic knockdown techniques including RNAi is required.
Proficiency in the use of molecular biology and protein biochemistry technologies, e.g. DNA cloning, Real-time PCR, protein-protein interaction, and enzymatic assays is preferred.
Demonstrated ability to evaluate and implement new techniques and technologies.
Experience mentoring and leading scientific associates.
Must be highly motivated, team-oriented, and have excellent interpersonal and communication skills. |
| Novartis Oncology |
na |
OH |
11/20/2009
|
| Territory Sales Manager - Toledo, OH |
| Minimum Education Required:
? Bachelor's degree or equivalent
Minimum Experience Required:
? 2-4 years successful outside sales experience
Preferred Level:
? One (1) year contact lens sales/opthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our ""New Hire Sales Training Program"". |
| Novartis Oncology |
na |
SD |
11/20/2009
|
| Territory Sales Manager - Sioux Falls, SD |
| Minimum Education Required:
? Bachelor's degree or equivalent
Minimum Experience Required:
? 2-4 years successful outside sales experience
Preferred Level:
? One (1) year contact lens sales/opthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our ""New Hire Sales Training Program"". |
| Novartis Oncology |
na |
OH |
11/20/2009
|
| Territory Sales Manager - Dallas, TX (East Dallas) |
| Minimum Education Required:
? Bachelor's degree or equivalent
Minimum Experience Required:
? 2-4 years successful outside sales experience
Preferred Level:
? One (1) year contact lens sales/opthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our ""New Hire Sales Training Program"". |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Territory Sales Manager - Brooklyn |
| Minimum Education Required:
? Bachelor's degree or equivalent
Minimum Experience Required:
? 2-4 years successful outside sales experience
Preferred Level:
? One (1) year contact lens sales/opthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our ""New Hire Sales Training Program"". |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Technician II, Lab |
| EDUCATION/EXPERIENCE:
High school diploma or equivalent required. Degree in physical sciences, statistics, or mathematics preferred. 3-5 years in a fast paced pharmaceutical environment and background in stability, statistics, chemistry or chemical analysis of pharmaceutical finished product dosage forms preferred. |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Technician II, Distribution |
| High School Diploma and 2 years related experience. Education: HS Diploma or equivalent required, some college preferred.
Work Experience: Proven commitment to customer service and a safe work environment. Must be team-oriented. Minimum 2-3 years of warehouse operational or manufacturing experience. Pharmaceutical experience is preferred, but not required. Strong attention to detail and accuracy. PC skills and inventory and shipping/receiving systems experience required; experience using SAP and Clippership preferred. Excellent communication (written and oral) and interpersonal (team building) skills. Minimum 2-3 years of fork-lift experience. |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Technical Manager CMO - Emeryville, CA |
| -Degree in related technical field (Biotechnology / Chemical Engineering / (Bio)chemistry) with doctorate (PhD) desirable or appropriate combination of education and experience.
-English fluent spoken and written; German & French spoken are a clear ?plus?
-Minimal 7-10 years confirmed experience in biotechnology manufacturing, ideally with direct responsibilities in manufacturing operations, 3rd-party management, toll-manufacturing activities or related area; Microbial expression system manufacturing background a plus. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Systems Consultant- Business |
| Principal Programmer
Responsible for all project level programming aspects (analysis datasets, pooled datasets, listings and tables) for drug project.
Major Activities:
1) Manage the programming activities for a global project following internal project management guidelines including resource planning.
2) Act as Program Programmer for assigned project and take a programming leadership role on the B & SR project team.
3) Maintain efficient interfaces with internal and external customers with advice from SR management.
4) Develop and comply with project/study standards and specifications following internal and regulatory guidelines.
5) Oversee programming style, quality of SR contributions and compliance with timelines.
6) Provide SR input and lead sections of Full Developments and Submission Working Groups.
7) Ensure the documents and specifications are consistent and comply with company standards by providing input into study protocol, CRF and data structures.
8) Program, according to specifications, analysis datasets, pooled datasets, listings summaries, figures and tables for Phase I-IV clinical trials and for SCS and SCE. Ensure quality control and quality audit of deliverables.
9) Maintain records for all assigned projects and archive trial/project analysis and associated documentation.
10) Participate in the selection of CROs, as required, and supervise SR project activities for CROs.
11) Train staff on trial and project level activities and internal processes.
12) Participate in or lead non-clinical project activities. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Systems Consultant - Business |
| Education :BA/BS or equivalent experience in mathematics, statistics computer science, life sciences or related field.
Languages: Fluent English (oral and written)
Experience/Professional requirements: (1) Expert knowledge of/experience with SAS software. (2) Good understanding of global clinical trials practices, procedures, methodologies.(3) Good understanding of regulatory requirements relevant to SR (e.g. GCP, ICH) (4) Experience in providing recommendations for maintenance or development of SR global policies, procedures and clinical data presentation standards. (5) Intermediate knowledge of office tools. (6) At least 8 years experience in a programming role preferably supporting clinical trials/ or in the pharmaceutical industry (5 years for MS Statistics/Computer Science graduates) |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Statistician II - Shanghai China |
| ? At least Master?s Degree in statistics or a closely related field.
? At least 2 year of experience in drug development (maybe acquired at a CRO) or a related area (no prior work experience required for Ph.D.).
? Good communication skills, including ability to communicate in English verbally and in writing.
? Ability to give effective guidance to programmers.
? Knowledge of and experience in using statistical software, in particular SAS
Work Location: Shanghai, China |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Programming Specialist |
| Education: BA/BS or equivalent experience in mathematics, statistics, computer science or life sciences or related field.
Languages: Fluent English (oral and written)
Experience/Professional requirement:: (1) Intermediate knowledge of /experience with SAS software. (2) Working knowledge of database. (3) Good understanding of global clinical trial practices, procedures, methodologies. (4) Good understanding of regulatory requirements relevant to SR (e.g. GCP, ICHP (5) Intermediate knowledge of MS Office tools. (6) At least 4 years experience in a programming role preferably supporting clinical trials/or in the pharmaceutical industry (2 years for MS Statistics/Computer Science graduates). |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Principal Biostatistician |
| Education Minimum/desirable): At least Masters Degree in Statistics (or equivalent degree with 6 years of experience or PhD with 2 years of experience.
Languages: Fluent English (oral or written).
Experience/Professional requirement:
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge preferably in relation to the specfic therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills.
6. Good team player. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Manager, IT Comm Ops |
| Education:
Bachelor?s degree in Information Technology or related field. Masters degree preferred.
Project Management certification
Experience:
Minimum 8 years of IT experience
Prior experience of IT operational management and team leadership
Experience in the US Pharmaceutical industry is required ? experience in the generics industry would be an advantage
Significant IT project management experience
Knowledge of SOX and GxP compliance |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Submissions Coordinator |
| Education:Minimum: bachelors degree with experience equivalent to graduate degree
Desirable: University degree (Diploma, Masters or Doctoral in life sciences, chemistry, business admin)
Languages:English fluent (oral and written)
Experience/Professional requirement:
? 3 years experience in Clinical Pharmacology, or Toxicology, or Preclinical Safety, or in any other TS discipline
? Advanced knowledge of CTD requirements
? Advanced knowledge of internal submission requirements and external regulatory requirements.
? Advanced knowledge of CREDI and PREDI
? Advanced knowledge of GXPs
? Prior submission experience
? Ability to lead multidisciplinary teams
? Advanced knowledge in all aspects of drug development
? Excellent oral and written communication skills
? Advanced knowledge of regulatory requirements and pharmaceutical development
? Working knowledge and compliance with the Good Laboratory Practices and Standard Operating Procedures
? Excellent organizational skills and advanced team-work skills with customer focus emphasis.
? Strong willingness and aptitude for learning and adapting new information and innovations |
| Novartis Oncology |
na |
NE |
11/20/2009
|
| Sr Scientist II |
| Degree(s) in chemistry or related disciplines. Typically requires minimum education and experience as follows:
Ph.D. with 2-6 years relevant experience, MS with 6+ years or BS with 8+ years.
? Thorough knowledge of chemical principles; Excellent analytical skills; Excellent written and communication skills; Thorough experience in analytical instrumentation, GMPs, and validation of analytical procedures; Should be creative and show initiative. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Sr Safety Assessment Expert |
| PhD in pharmacology, toxicology or a related biological science; MD with appropriate experience, DVM with appropriate training and experience. PharmD or equivalent with a strong biological background or equivalent work experience.
Languages: Fluent English (oral and written).
Experience/Professional requirement:
1. Level-dependent.
o Base level: At least 2 years experience as a part-time safety assessment project team representative alongside other duties such as study director; experience with biologicals safety assessment desirable.
o Senior level: At least 3 years experience as a full time safety assessment project team representative, preferably with a mix of research, exploratory development and full development teams including experience of biological products
o Principal level: At least 5 years experience as a senior level safety assessment PTR and internal recognition as an opinion leader in one or more aspects of safety assessment, or the equivalent experience in a similar external organization. Experience of biologics safety assessment required.
2. Advanced knowledge of the many scientific disciplines involved in biopharmaceutical drug safety assessment and the relevant laboratory tools and procedures related to safety assessment and risk management, including PK-PD aspects of study design and data interpretation
3. Documented expertise in scientific and technical problem-solving in an international, multi-disciplinary, project-driven environment.
4. Proficient with full range of techniques used in job and core area?especially with communication and negotiation with global health authorities.
5. Detailed knowledge of drug development processes and worldwide regulatory guidelines and procedures.
6. Ability to manage conflicting expectations in a matrix environment.
7. Proven negotiation skills.
8. Excellent program and project management skills.
9. Team player behavioural attributes.
10. Self-motivated and able to operate independently.
11. Ability to coach and advise colleagues in project-related matters (at senior and principal levels). |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Principal Biostatistician |
| Education Minimum/desirable): At least Masters Degree in Statistics (or equivalent degree with 6 years of experience or PhD with 2 years of experience.
Languages: Fluent English (oral or written).
Experience/Professional requirement:
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge preferably in relation to the specfic therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Principal Biostatistician |
| Education Minimum/desirable): At least Masters Degree in Statistics (or equivalent degree with 6 years of experience or PhD with 2 years of experience.
Languages: Fluent English (oral or written).
Experience/Professional requirement:
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge preferably in relation to the specfic therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills.
6. Good team player. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr CTH/CTH (nonMD) |
| ? ? 6 years technical, operational and managerial experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organisation.
? Experience in multiple clinical indications and/or TAs is preferable.
? Previous experience leading in parallel several trials; leading multidisciplinary trial teams in a complex matrix environment (including remote).
? Demonstrated ability to establish effective working relationships with key investigators.
? Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and global clinical development process.
? Advanced knowledge of the assigned TA is preferred, with the demonstrated capability to interpret, discuss and represent trial or program level data.
? Previous experience in interactions with Health Authorities is preferable.
? Experience in Neuropsychiatric disease areas preferred (i.e. Schizophrenia, bipolar disorder, depression) |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Sr Admin Asst, Strategic Planning & Operations |
| Minimum 5+ years of solid administrative experience; experience in pharmaceutical and/or healthcare environment preferred
? Excellent interpersonal and written/oral communication skills required
? Some college preferred or related equivalent experience
? The ability to manage multiple assignments with competing priorities in a fast-paced environment is essential
? Must be proactive, efficient, customer-focused and have the ability to work independently
? Must be able to interact effectively with all levels of employees within TS, including international colleagues, and disseminate information in a timely and effective manner.
? Ability to be resourceful, obtain information from the Intranet, and learn new software programs quickly
? Must have proficiency and relevant experience with word processing, spreadsheets, and project management programs. (e.g. MS Office-Word, Excel, PowerPoint, Concur, Lotus Notes, etc.).
? Ability to work in a team environment, attention to detail and strong organizational skills are necessary.
? You must be able to handle confidential information and communicate with all levels of management in both NIBR and Development in a professional manner. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Software Developer/ Architect |
| ? Advanced degree in Computer Science from reputable program with top performance.
? Experience building commercial quality web-based software solutions at significant scale with the most advanced tools including both Microsoft-centric and Java-centric platforms.
? Demonstrated ability to work well as part of a high performing software engineering team.
? Interest in intersection between the life sciences and computer science.
? Willingness and ability to use variety of tools in very heterogeneous environment to achieve science and business goals.
? Experience building and managing ?big data? systems- Strong communications and interpersonal skills |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Scientist (Pharmacokinetics) |
| M.S. degree in biological or related sciences with minimal 3 years laboratory experience. Research experience using animal models is mandatory. Small animal surgical experience is highly desired. Excellent verbal and written communication skills are essential. The knowledge of radiochemistry, tissue distribution, metabolism and pharmacokinetics is desirable. Prior work experience with PK/PD analysis and a demonstrated ability to work with modeling tools and databases (e.g. WinNonlin, GastroPlus, Watson, Spotfire, etc) is a plus.
THIS REQUISITION APPROVED BY TSLT ON 1-JULY-2009 AND MOVED TO CRITICAL HIRE LIST. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Scientific Expert: Development Licensing & Evaluation |
| University degree (diploma, PhD or MD)
1. 8 years experience within pharmaceutical industry
2. 3 years of Project management or cross functional experience
3. Advanced level of the basic science. Bring an expert level of understanding in a functional area
4. Thought Leader for the drug dev. process; expert at aligning development program goals with business needs
5. Advance knowledge of business, competitive environment and of international business practices
6. Advanced planning and tracking skills, able to see big picture, well-organized, focused on results
7. Expert leadership skills demonstrated in GPT, in staff management role or in other organizational assignments. Expert skill to optimize contribution of team members as individuals and members of a cohesive team.
8. Strong interpersonal and communication skills for bridging between scientific and business participants, for negotiating timelines and for effective international collaboration. Strong verbal communication. Expert in written communications. Strong, critical and objective interpretation of scientific and commercial information. Expert team player |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Roles-Regulatory Affairs, R&D |
| 10+ years extensive Regulatory Affairs experience. An academic background in biological/medical sciences (preferably MD or PhD), strong diplomatic skills for dealing with regulatory agencies ability to realize a vision by inspiring and motivating others, ability to thrive and grow in a fast-paced, intellectually challenging environment, are additional important requirements. Candidate should be fluent in English. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Senior Manager, Nucleic Acid Technology Chemistry & Testing |
| At least five years of In Vitro Molecular Diagnostic Product/Sample Prep/Assay development experience with a successful track record of regulatory submission and/or product launch. Minimum of five years of supervisory and managerial experience including budgeting, project planning, resource allocation, and staff development. Demonstrated technical proficiency and ability to collaborate with others across functional disciplines. Experience in Design for Six Sigma (DFSS) is highly desirable. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Senior Manager, Nucleic Acid Technology Chemistry & Testing |
| At least five years of In Vitro Molecular Diagnostic Product/Sample Prep/Assay development experience with a successful track record of regulatory submission and/or product launch. Minimum of five years of supervisory and managerial experience including budgeting, project planning, resource allocation, and staff development. Demonstrated technical proficiency and ability to collaborate with others across functional disciplines. Experience in Design for Six Sigma (DFSS) is highly desirable. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior CQA Compliance Specialist |
| BA/BS or equivalent.
English (optimally a second universal language preferred).
5+ years clinical/industry/health authority experience with at least 2 years GCP auditing experience.
30-40% travel.
Ability to manage and objectively evaluate compliance issues.
Ability to maintain a moderate degree of independence with respect to decision making and problem solving.
Excellent verbal and written communication skills, team player, interpersonal skills.
Excellent computer skills, including Excel, Word, etc.
Thorough knowledge of the clinical development, clinical research processes and drug registration process/requirements required.
Thorough knowledge of GCP regulations and guidelines as well as in applicable Novartis SOPs/NIPs and Business Practices.
Good knowledge of computer validation and Part 11 requirements.
Previous experience identifying training needs, developing and conducting training programs.
Ability to multi-task and function independently as required.
Ability to operate successfully in various team capacities, including leader and/or active member.
Ability to operate successfully in various cultural environments.
Ability to coach and mentor.
Auditor certification a plus. |
| Novartis Oncology |
na |
CO |
11/20/2009
|
| Senior Buyer/Planner |
| Educational/Professional Requirements:
BS/BA with 3-5 years purchasing experience
Knowledge equivalent to and/or receipt of ISM or APICS certification
Skills & Competencies:
? Working knowledge of MRP/MPS methodology and understands inputs and outputs of a material requirements planning system (MRP).
? Demonstrated knowledge and ability to use common software tools such as spreadsheets and word processors.
? Effective planning and organizational skills to ensure all tasks are completed within prescribed timelines.
? Effective written and oral communication skills.
? Problem solving skills to address supply issues within this position?s means of delegated authority.
Physical Demands:
This position requires close and distance vision, occasional lifting up to 25 pounds, and being seated a majority of the time.
Work Environment:
Typical office enviornment with moderate noise levels. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Senior Biostatistician |
| Provide statistical consultation and analysis in support of research & development, clinical testing, and manufacturing of Novartis MDx products.
The incumbent will:
-Have Ph.D. or Master?s with 5+ years in Statistics or Biostatistics
-Support internal clients through out MDx.
-Represent Biostatistics on project teams and serve as primary liaison to key internal clients with regard to resource needs and timelines.
-Interact with FDA or other regulatory agencies as needed in statistical aspects of study design, data analysis and statistical procedures; interpret the project implications of regulatory guidelines.
-Manage, mentor direct reports, and provide them opportunities for their self development
-Develop Biostatistics procedures and guidelines to comply with corporate quality polices
-Provide technical leadership and initiate methodological research to improve the methods current in use. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| SDC Compliance Associate - Quality R&D |
| BS/MS in a science field with 8-10 years experience in the pharmaceutical industry.
o Good knowledge and understanding of all GMP related requirements, proficiency of regulatory and ICH guidelines
o Broad experience in the pharmaceutical industry with a strong analytical and/or manufacturing background, some R&D a plus.
o Detail oriented with Quality Assurance background with good problem solving acumen.
o Ability to work effectively in a team environment with great organization skills
o Excellent communication skills
o Critical thinking, process and performance oriented. Constant drive to improve working practices
o Provision of timely and accurate documentation to minimize submission deficiencies
o Proven performance in review of key documents by highlighting areas of deficiencies and aiding in remediation of the documentation.
o Timely follow-up and closure of Deviations, Investigations, Change Controls and CAPAs.
o Initiation of trainings and/or other appropriate measures to enhance quality and compliance within department
o Escalation of issues/alerts as appropriate to Upper Management and proposal of corrective actions |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Scientist, Pharmacokinetics |
| EDUCATION/EXPERIENCE:
Ph.D. with 1-3 years or MS with 5-8 years of experience in one or more areas biopharmaceutics, pharmacokinetics, drug metabolism, bioanalytical chemistry, biostatistics, PK modeling, in vivo-in vitro correlation (IVIVC), and clinical endpoint BE study design/conduct. Inhalation experience a plus. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Scientist, NPKPD |
| M.S. degree in biological or related sciences. Research experience using animal models is mandatory. Small animal surgical experience is highly desired. Good verbal and written communication skills are essential. The knowledge of radiochemistry, tissue distribution, metabolism and pharmacology is desirable. Prior work experience with PK/PD or statistical analysis and a demonstrated ability to work with modeling tools and databases (e.g. WinNonlin, GastroPlus, Watson, Spotfire, etc) is a plus. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientist-Biochemical & Organ Toxicology |
| Technical Skill Sets
? Good skills in isolating and cultivating cells from different organs in different species
? Good skills in performing a variety of biochemical techniques (e.g., preparation of cell and tissue extracts, subcellular fractionation, enzyme assays, ELISA, Western blots, ?).
? Good skills in performing a variety of molecular biology techniques (e.g. nucleic acid purification, cloning, PCR)
? Good understanding of SOPs as well as their practical implementation
? Fluency in English
? Working knowledge of relevant IT systems
Experience
? At least 3 years of experience in cellular biology or toxicology in either academic or industrial environment
? Working experience with mammalian cell culture models (primary cultures and cell lines) and related techniques
? Working experience in molecular & biochemical analytical techniques
Personal Skill Sets:
? Interpersonal and teamwork skills
? Good oral communication and writing skills
? Computer skills for experimental organization, assay design, data collection and analysis, and report writing
Education
Bachelor or Master degree in life sciences, preferably biochemistry, pharmacology or biology. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientist I, Mammalian Cell Line Development |
| A B.S. or M.S. degree in biology, cell biology, immunology, or related life science field and 3 plus years of experience in biotechnology or pharmaceutical industry are required.
Recent Ph.D. graduates will also be considered.
The Scientist must be able to work independently to design experiments and perform therapeutic protein expression and production runs to accomplish team goals. Candidate should bring a highly collaborative spirit with an ability to work on multiple projects and maintain well organized records and notebooks.
The successful candidate should also have excellent written and oral communication skills, and be able to thrive in our fast-paced and dynamic organization. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientist - Animal Models Laboratory |
| The preferred candidate will therefore have strong experience in animal experimentation design and execution, drug administration, and small animal surgery. The preferred candidate will have knowledge of mechanisms of drug pharmacology and toxicity and biological approaches to study such mechanisms.
Specific responsibilities include execution of diverse animal experiments. The candidate will help the AM Lab Head plan, interpret and present experimental results. The candidate is expected to work autonomously, requiring minimal guidance on major activities, and to collaborate productively and cooperatively with Laboratory Animal Support (LAS) services. Secondary responsibilities include laboratory maintenance, ordering, oversight of junior technical staff, regular participation to project team meetings as assigned, maintaining orderly and up-to-date laboratory records in accordance with best practices for a GLS-practicing (GLP-like) laboratory.
BA, BS, MS required in life sciences or relevant related field. Medical, surgical, veterinary, or specialized animal experimental training is preferred.
Experience
- In vivo pharmacology.
- Small animal surgery.
- Coordination and cooperation with existing animal study support services and personnel.
- Laboratory Management.
- Molecular & cellular biology skills/techniques.
Technical Ability
- Drug administration to animals, including PO, IV, IP.
- Small animal surgery, such as adoptive cell transfer, vascular dissection, etc.
- Collection of body fluids from living small animals, such as urine and blood.
- Small animal necropsy and tissue collection.
- Molecular and biochemical techniques, such as PCR-based genotyping, qPCR, Western blotting, ELISA, and multiplex immunoassays
- Laboratory maintenance.
- Cost and inventory control at the laboratory level.
- Excellence in data summarization.
Presentation
- Excellent oral and written communication skills. Able to independently summarize role of team, experimental approaches and findings, and potential value.
- Able to present and defend data in lab meetings, as well as during external liasing and project team meetings.
- Able to prepare written reports, for AM, Translational Toxicology, iTox, and external consumption.
Three-five years minimal required years of experience
Rational/Justification: Senior Scientist Technical position essential to support work in the laboratory. Translational Safety Biomarkers and Animal Models (TSBAM) is a new laboratory with a mission to provide innovative, fit-for-purpose animal models for project-driven safety studies. We have hired only the Lab Head of the Animal Models Lab, and lack technical support for delivery of defined objectives. This technical position is prioritized to support the Lab activities aligned with the overall safety strategy, and to move high priority activities forward. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| SAP NetWeaver Java Application Architect |
| - University degree or equivalent in Information Technology experience
- more than 6 years of IT experience out of which last 4 years in the development and design of SAP NetWeaver Java applications (SAP Enterprise Portal and Composition Environment)
- Experience in design and governance of SAP NetWeaver Java development processes and standards desired
- Active participation in at least 2 complete implementation project cycles from blue print till post go-live support as a SAP NetWeaver Java developer
- In-depth knowledge and working experience with Enterprise Portal, Composition Environment and NetWeaver Development
- Sound knowledge of the SAP NetWeaver technology platform and related products (SOA, ESR and others)
- Java background
- Knowledge of ABAP programming language advantageous
- Excellent communication skills with a strong customer focus
- Excellent analytical skills, solution and target oriented |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sales Representative/Consultant - Red Bank, NJ - 1ZEK1C |
| A Bachelor's Degree * Outside sales experience with documented success in business-to-business sales preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program.
Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sales Representative/Consultant - Morristown, NJ - 1ZEB4B |
| A Bachelor's Degree * Outside sales experience with documented success in business-to-business sales preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program.
Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
OH |
11/20/2009
|
| Sales Representative - Toledo South, OH - 3ZAE4B |
| A Bachelor's Degree * Outside sales experience with documented success in business-to-business sales preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program. Novartis is an equal |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sales Consultant/Sr. Sales Consultant - New Brunswick, NJ - 1ZEK4A |
| A Bachelor's Degree * Outside sales experience with documented success in Long Term Care and or Account Management experience. Alzheimer selling experience preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program.
Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Research Scientist-Pre-clinical MRI |
| A BS/MS or PhD degree in Bioengineering, or related field.
A minimum of one year experience with small animal Magnetic Resonance Imaging is required. PET experience is a plus. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Research HSE Risk Manager |
| This position requires 3-5 years experience in health, safety, and environmental risk assessment and management in a biotech/ pharma laboratory environment. The successful candidate should have experience in implementation and maintenance of HSE audit systems, development of tools and programs, and will have conducted periodic audits and follow up for corrective measures.
Bachelor degree in life sciences, chemistry, or other appropriate discipline and ABSA certification as a Certified Biosafety Professional (CBP) or other equivalent certification in Occupational Health and Safety Program is required. Solid verbal and written English communication skills. Fluency in additional languages, such as German or Mandarin would be favorably considered. Demonstrated leadership abilities, as well as the ability to communicate and influence others in a complex, matrixed environment are essential. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Research Associate ? X-ray crystallography |
| B.S/M.S. or equivalent in biochemistry or a related discipline with at least 2 years of research laboratory experience. Experience in protein chemistry (e.g. expression, purification and characterization) is required. Experience with protein crystallization, x-ray data collection, and/or biophysical characterization of proteins would be a decided asset. The candidate must possess good oral and written communication skills. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Regulatory CMC Liaison / Biologics |
| Minimum:
Relevant scientific degree in biotechnology, biochemistry and cell biology or equivalent.
Languages:
Fluent English required (oral & written).
Experience / Professional Requirements:
? Several years of experience in regulatory preferred.
? Excellent working knowledge/experience in regulatory submissions and approval processes for Biopharmaceuticals and ability to deal with complex CMC regulatory issues and requirements
? Strong background in biopharmaceutical development (e.g. cell culture, downstream processing, analytics). Biologics experience desired
? Proven track record in successfully leading/working in interdisciplinary teams, and of planning, coordinating and leading activities simultaneously on multiple projects.
? Strong interpersonal, organizational, communication, presentation, negotiation and problem solving skills. |
| Novartis Oncology |
na |
HI |
11/20/2009
|
| Regl Scientific Mgr/Dir (Hawaii) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 3 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare/ managed markets environment.
Field-based medical and/or managed care with teaching experience preferred. Thorough knowledge of clinical medicine, managed markets, pharmacoeconomics, disease management, and medical research. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science-oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Operating Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Salary flexible. |
| Novartis Oncology |
na |
UT |
11/20/2009
|
| Regl Account Scientific Asc Dir/Director (AZ, CO, NM, NV and UT) |
| Position will be filled at level commensurate with experience.
MD, PharmD, or PhD with 4 years Post-Doctoral experience required. Field-based medical and/or managed care experience preferred. Thorough knowledge of clinical medicine, managed markets, pharmacoeconomics, disease management, and medical research. Excellent interpersonal communication and presentation skills, (including ability to network), strong personal integrity, teamwork abilities and a customer focus are necessary. Must possess a thorough understanding of the FDA, OIG, HIPAA, and GCP/ICH guidelines relevant to the pharmaceutical industry. Must be able to organize, prioritize, and work effectively in a constantly changing environment. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Ability to interface effectively with a variety of technical platforms for the collection, review, and dissemination of medical information. Demonstrated record of scientific/medical publication. Demonstrated knowledge of GCP practices and standards. Demonstrated technical expertise in at least one disease or therapeutic area. The RASM/D position is associated with approximately 60% travel. Salary flexible. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Regional Associate Director US Clinical Operations, Oncology |
| ? BS degree in a scientific or health care discipline.
? Expert in Oncology with established contacts in the medical community
desired
? Demonstrated skill sets, competency, and proficiency in clinical research
and relevant people management skills.
? Thorough understanding of international aspects of the drug development
process
? Extensive knowledge of GCP/ICH, FDA, local regulations, and trial
monitoring practices
? Matrix management skills in a local and global environment
? Excellent writing, oral and interpersonal communication skills as well as
strong organizational skills
? Proficiency in relevant computer software applications
? Ability to travel a minimum of 50%
? Ability to interact/communicate in matrix organization.
? At least 6 years experience in clinical research.
? At least 2 years supervisory experience is preferred.
? At least 5 years monitoring experience is preferred.
? Experience in project management a Plus
? Strong computer knowledge in Word, PowerPoint, Excel and Lotus Notes
At least 6 years |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| QC Chemist IV |
| EDUCATION/EXPERIENCE
BS or BA in Chemistry or life sciences and 8 or more years of professional related |
| Novartis Oncology |
na |
CO |
11/20/2009
|
| QC Chemist - Temporary |
| BS/BA in Chemistry or life sciences
? Knowledge of applicable processes, regulations and guidance documents; testing and documentation requirements, equipment use, preventive maintenance and troubleshooting.
? Proven ability to work in a team environment through conflict resolution and negotiations. Excellent written and verbal communication skills.
? Adherence to all health, safety & environment requirements in support of departmental and site HSE goals.
? Works in a safe and efficient manner. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Project Manager, Novartis Biologics |
| A PhD in life sciences or a MS degree with scientific experience equivalent to PhD required.
Strong knowledge of basic science and the drug discovery and development process for biopharmaceuticals.
A minimum 5 years in pharmaceutical industry, with demonstrated project management skills and experience in cross-functional settings. Up-to-date understanding of the drug discovery and drug development process for biological therapeutics.
Expert planning and tracking skills, capable of managing multiple early projects with ease, well-organized, excellent time management with respect to priorities and self-management.
Strong problem solving skills for maintaining project timelines and developing alternate development scenarios and creative solutions to problems.
Excellent negotiation skills; Strong interpersonal and communication skills for bridging between drug discovery, early and late Development participants, for negotiating timelines and for effective international collaboration.
Strong verbal and written communication skills.
Strong, critical and objective interpretation of scientific information. Strong analytical skills for integrating and interpreting interdisciplinary project information. |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Production Associate 2 |
| Requires handling of chemicals such as acids, alkalis, solvents and powdered media; Must be able to wear a negative pressure based respirator; Able to work in noisy environments that may exceed 80 decibels; May be required to lift up to 50 pounds multiple times in the work shift (e.g. 1-5 times in a hour); Requires pushing and pulling of equipment (e.g. drum dollies with 55 gallon drums or 500 liter portable tanks) throughout the work shift (e.g. 1-5 times in a period of 1 hour); Requires bending and reaching throughout the work shift in support of wide range of activities such as valve adjustment, fastening of hoses and/or connections and con-ducting cleaning activities; May require climbing up and down flights of stairs during the work shift (e.g. 1-4 times in a hour) as well as ascending a fixed or portable ladder to heights up to twenty feet; Requires walking / standing for extended periods (up to 6 hours) throughout the work shift; Must be able to enter confined spaces such as tanks and pits; Must be able to op-erate powered industrial trucks and/or motor vehicles throughout the work shift (e.g. driving periods up to 2 hours).
Minimum of 5 years experience with a H.S. diploma or 1 to 3 years experience with a Bachelors degree. Experience in GMP manufacturing or research and development is required. |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Production Associate 2 |
| Requires handling of chemicals such as acids, alkalis, solvents and powdered media; Must be able to wear a negative pressure based respirator; Able to work in noisy environments that may exceed 80 decibels; May be required to lift up to 50 pounds multiple times in the work shift (e.g. 1-5 times in a hour); Requires pushing and pulling of equipment (e.g. drum dollies with 55 gallon drums or 500 liter portable tanks) throughout the work shift (e.g. 1-5 times in a period of 1 hour); Requires bending and reaching throughout the work shift in support of wide range of activities such as valve adjustment, fastening of hoses and/or connections and con-ducting cleaning activities; May require climbing up and down flights of stairs during the work shift (e.g. 1-4 times in a hour) as well as ascending a fixed or portable ladder to heights up to twenty feet; Requires walking / standing for extended periods (up to 6 hours) throughout the work shift; Must be able to enter confined spaces such as tanks and pits; Must be able to operate powered industrial trucks and/or motor vehicles throughout the work shift (e.g. driving periods up to 2 hours).
Minimum of 5 years experience with a H.S. diploma or 1 to 3 years experience with a Bachelors degree. Experience in GMP manufacturing or research and development is required. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Principal Scientist (GMP Facility Manager/Engineer) |
| Education
Minimum: BS/MS or equivalent with greater than 8 years of experience.
Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent) with a minimum of 5 years of experience.
Languages: Fluent English (oral and written)
Experience/Professional Requirement:
1. Successfully demonstrated several years (minimum of 3 years) of directly related experience as senior scientist of Ph.D. with post-doctoral/industrial experience (minimum of 1 year) or equivalent.
2. Successfully demonstrated expertise in a specific scientific/technical area.
3. Recognized achievements in the development of new lab/plant procedures.
4. Excellent knowledge of laboratory and/or technical tools.
5. Proficient in utilization of special tools/equipment, lab automation tools and specialized facilities e.g., containment/sterile labs.
6. Thorough understanding of development activities and processes in a specific function.
7. Good knowledge of software and computer tools.
8. Profound literature search skills.
9. Good presentation skills and scientific/technical writing skills.
10. Strong scientific leadership skills.
11. Strong knowledge of relevant SOP, GLP, GMP and Novartis regulations and policies. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Presidential Post Doctoral Fellow |
| Multiple positions exist at all sites of Novartis Institutes for BioMedical Research for individuals with the following minimum requirements: Ph.D. in biological sciences, chemistry, or computer science. Applicants who have commenced postdoctoral training may apply as well, but they should not have been in postdoctoral training for more than 3 years. Candidates must be able to work independently and also participate in team efforts. Excellent oral / written communication and presentation skills and scientific creativity are essential. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Postdoctoral Fellow, DMPK |
| Ph.D. degree with 0-3 years of post-PhD research experience in pharmacokinetics, biopharmaceutics, biomedical engineering, chemical engineering, or other related discipline with specific experience in PK/PD and/or PK modeling is required. The candidate must be able to work independently and have a strong understanding of PK/PD. The candidate should should be able to provide technical assistance on individual projects, spanning across multiple therapeutic areas. Hands-on experience in PK and PK/PD modeling is a must. Good oral and written communication skills are required. Previous experience with some of the PKPD softwares such as: WinNonlin; ADAPT; NONMEM, GastroPlus. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| PhD Scientist: Antibody Therapeutics |
| Molecular Biology lab head Qualifications:
? Ph.D. in molecular biology or life science
? Minimum 3 years of post-doctoral experience in life-science and/or antibody therapeutic research. Industry experience is a plus.
? Self-driven and creative personality
? Excellent written and oral communication skills
? Extensive experience in molecular biology, cell and biochemical assay development and analysis |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Pharmacovigilance Leader (PVL MD) |
| Experience/Professional:
3 years clinical experience postdoctoral
requirement:
At least 3 years in drug development in a major pharmaceutical company including 2 years in drug safety at an operational or medical position
Proven ability to analyze, interpret, discuss, and represent safety information both in writing and orally.
Experience in preparing or contributing to preparation of clinical safety assessments and regulatory reports/submissions involving safety information.
Experience with (safety or others) issue management
Experience in drug development, clinical trial methodology, regulatory requirements, scientific methodo logy, statistics and writing of publications
Education (minimum/desirable): Medical Degree required. Specialty Board certification desirable. Useful additional degrees: Post graduate degree in Pharmaceutical Medicine; Master of Public Health in Epidemiology (or equivalent) |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Pharmaceutical Sales Representative- Los Angeles, CA 5ZDL1A |
| A Bachelor's Degree * Outside sales experience with documented success in business-to-business sales preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Ph.D Scientist: Oncology Biotherapeutics |
| Biotherapeutics lab head Qualifications:
? Ph.D. molecular biology or related field.
? Minimum 3 years of post-doctoral experience in cancer and/or antibody therapeutic research.
? Independent, self motivated and innovative personality
? Excellent written and oral communication skills
? Extensive experience in cell and biochemical assay development and analysis |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Pathways Research Scientist (BS/MS) |
| ?BS or MS in Biochemistry, Molecular Biology, or Cell Biology, with 5+ years of laboratory research experience.
? Extensive experience with culturing various mammalian cell lines, utilizing both 2D and 3D culture systems, designing cell-based assays, generating stable cell lines, and executing small molecule screens with laboratory automation equipment.
? Experience with high content imaging and designing/executing high content imaging-based screens.
? Outstanding molecular biology techniques including complex DNA cloning, site-directed mutagenesis, and qPCR.
? Exceptional expertise in genetic screening with siRNA/shRNA/cDNA by conventional and viral transduction technologies.
? Proficient in various protein analysis techniques, including, but not limited to, ELISA assays, immunoprecipitations, and western blots.
?Excellent communication skills |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Operator - Vacaville, CA Biopharmaceutical Operations |
| Requires handling of chemicals such as acids, alkalis, solvents and powdered media; Must be able to wear a negative pressure based respirator; Able to work in noisy environments that may exceed 80 decibels; May be required to lift up to 50 pounds multiple times in the work shift (e.g. 1-5 times in a hour); Requires pushing and pulling of equipment (e.g. drum dollies with 55 gallon drums or 500 liter portable tanks) throughout the work shift (e.g. 1-5 times in a period of 1 hour); Requires bending and reaching throughout the work shift in support of wide range of activities such as valve adjustment, fastening of hoses and/or connections and con-ducting cleaning activities; May require climbing up and down flights of stairs during the work shift (e.g. 1-4 times in a hour) as well as ascending a fixed or portable ladder to heights up to twenty feet; Requires walking / standing for extended periods (up to 6 hours) throughout the work shift; Must be able to enter confined spaces such as tanks and pits; Must be able to op-erate powered industrial trucks and/or motor vehicles throughout the work shift (e.g. driving periods up to 2 hours).
Minimum of 5 years experience with a H.S. diploma or 1 to 3 years experience with a Bachelors degree. Experience in GMP manufacturing or research and development is required. |
| Novartis Oncology |
na |
|