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Search Jobs by Category
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Director**- Clinical Research- Brilinta Brand Team |
Requirements ? Education and Experience**
· Graduate of a recognized school of medicine with an M.D. degree or equivalent.
· Specialty training and board certification in Internal Medicine; Specialty Certificationin Cardiovascular Medicine highly desireable.
· Three or more years of Drug Development experience obtained while working in the pharmaceutical industry with focus and expertise in cardiovascular disease especially in the area of thrombosis. Exceptionally well qualified candidates without prior pharmaceutical company experience may be considered.
· Prior clinical experience and strong academic track record in cardiovascular disease required.
· Experience in designing, monitoring and implementing clinical trials and interpreting trial results, including understanding of biostatistics, safety reporting, and regulatory requirements
· An understanding of pharmaceutical industry R&D, particularly of major clinical milestones and of the factors which influence those decision points.
· An understanding of the interplay between clinical development and commercial objectives.
· Excellent presentation skills.
** Please note: Depending on experience, this role may be modified to that of the Associate Direrctor or Senior Director level.
 |
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Director** Clinical Research- Crestor/Certriad Brand Team |
| · Graduate of a recognized school of medicine with an M.D. degree or equivalent.
· · Specialty training and board certification in Internal Medicine; Pediatrics (with appropriate subspecialty); Endocrinology; Diabetes and Metabolism; or Cardiovascular Medicine .
· Three or more years of Drug Development experience obtained while working in the pharmaceutical industry for Director level position. Exceptionally well qualified candidates without prior pharmaceutical company experience may be considered.
· Prior clinical experience and strong academic track record in cardiovascular disease required.
· Experience in designing, monitoring and implementing clinical trials and interpreting trial results, including understanding of biostatistics, safety reporting, and regulatory requirements
· An understanding of pharmaceutical industry R&D, particularly of major clinical milestones and of the factors which influence those decision points.
· An understanding of the interplay between clinical development and commercial objectives.
· Excellent presentation and interpersonal skills skills.
** Please note: Depending on experience, this role may be modified to that of the Associate Direrctor or Senior Director level.
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| 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
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| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Pharmacometrician |
| (These may vary slightly with specific prior research experience, but will generally be as follows)
? Has a MSc, PhD or post graduate qualification and/or qualification as a Clinical Pharmacokineticist or Pharmacometrician according to a recognized official training program
? 4-7 years post-graduate experience in relevant disciplines (Pharmacokinetics, Pharmacometrics and/or pre-clinical research or academic research)
? 1-3 years experience in drug development (preferably obtained from a pharmaceutical company or contract research organization)
Skills and Capabilities
? Good oral and written communication skills with a demonstrated ability to write protocols, clinical trial reports and scientific peer-reviewed publications
? Understanding of Good Clinical Practice ? Good presentation skills
? Knowledge of opinion leaders in area of expertise
? Broad understanding of drug discovery and development
? Familiarity with regional and international regulatory requirements relevant to clinical pharmacology. Good understanding of major commercial drivers.
? Familiarity with relevant preclinical and clinical research methods
? Demonstrated expertise in use of relevant analytical tools (e.g. WinNonlin, NONMEM, SAS, S-Plus, R)
? Knowledge of key opinion leaders in pharmacokinetics / pharmacometrics; ability to access external expertise and resources as necessary
? Ability to effectively represent the Company to key external stakeholders
? Ability to make complex judgments, develop innovative solutions, and apply comprehensive cross-functional and industry understanding to individual projects and programs
? Proactive and able to function autonomously
? Cultural sensitivity
? Ability to influence ? through effective communication, respectful challenge, and persuasion rather than dictate ? the beliefs, opinions and behaviors of key customers and others at a senior level across the business.
? Able to respond to changes in the internal and external environments by adjusting plans or developing new ways of working
? Excellent team-working skills
? Ability to effectively engage with a wide variety of technical and business experts
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| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Mechanic II |
| ? High school diploma
? 3 years of active, hands-on experience in the installation, maintenance, repair and troubleshooting of refrigeration and HVAC/R equipment in commercial, industrial, manufacturing or research facilities.
? Completion of two or more years of a state accredited Journeyman program in HVAC/Refrigeration or equivalent technical program.
? Demonstrated ability with analytical/troubleshooting skills in HVAC controls (DDC and pneumatic) and refrigeration equipment
? Possess a valid EPA 608 Universal Certificate
? Demonstrated ability to make sound decisions and deal effectively with internal customers independently.
? Demonstrated ability to successfully complete complex assignments from start to finish
? Demonstrated ability to work independently and using safe work practices.
? Strong teamwork, interpersonal, communication, and writing skills
? Basic computer skills.
Preferred Background
? Completion of a state accredited Journeyman program or equivalent Associates degree in an HVAC engineering technology program
? 5+ years of active, hands-on experience in the HVAC/Refrigeration trade
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| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Counsel |
| ? Law Degree
? 3-7 years of corporate/commercial legal experience including legal practice experience with pharmaceutical or biotech industry. Ability to handle routine and moderately complex legal aspects of pharmaceutical commercial matters with limited supervision and direction.
? Strong counseling and negotiation skills and experience in effectively working in groups.
? Ability to build and maintain effective relationships with clients and colleagues through strong interpersonal and communication skills and consistent demonstration of solid professional judgment.
Preferred Background:
? Working knowledge and general familiarity with FDA and the law relating to the approval, sale and marketing (including the federal and state anti-kickback laws) of pharmaceutical products.
? Experience in reviewing and providing advice on DTC advertising, health care professional promotional materials and disease state materials and other pharmaceutical marketing initiatives.
? Experience with reviewing and counseling on legal issues related to advisory boards, speaker programs, and other similar engagements.
? Working knowledge of the drug approval process and experience with related legal issues.
? Previous experience in legal department of corporation or other business or major law firm.
? Experience in drafting and negotiating contracts and other transactional experience.
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| IS Architecture Sr. Manager (Domain Architect; Enterprise Content Management) |
| ? Bachelor?s degree in relevant field.
? Minimum 10 years cumulative experience in architecture and supporting methodologies, with at least 5 years in the domain(s) of focus
? A broad understanding of architecture covering all aspects from business/process, information, application to infrastructure architecture.
? Working knowledge of necessary operating model components to support architecture implementation and adoption.
? Strong analysis, conceptual thinking and modeling capabilities.
? Strong relationship management, strategic influencing, and communication skills.
? Delivery focused and creative in finding ways of delivering.
? Ability and desire to work globally and see this as a great opportunity.
? Ability to work independently across the global organization while overseeing the work of others.
Preferred Background
? Advanced degree in relevant field
? Large scale project management experience
? Cross-functional team experience
? Evidence of strong leadership
? Accomplished facilitation and negotiating skills
|
| AstraZeneca Pharmaceuticals |
Framingham/Worcester |
MA |
11/19/2009
|
| Finance Director; WB Supply Site |
| ? Bachelors Degree in Accounting
? 10+ years experience in finance and/or accounting.
? Strong analytical skills, ability to develop and analyze complex issues.
? Strong knowledge of pharmaceutical manufacturing and cost accounting. Prior exposure to general operations, MRP, inventory planning and control, and accounting services is desirable.
? Demonstrated ability to lead and participate in teams.
? Experienced in partnering with other functions to achieve success.
? Excellent interpersonal, decision making, organizational & management skills.
? Demonstrated ability to successfully work in a dynamic work environment.
? Strong knowledge of information systems is required in order to develop, implement and maintain new systems and incorporate production-processing changes into existing systems.
Preferred Background:
? CPA, MBA, or Master?s Degree in a relevant field.
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| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Primary Reviewer Director; PRA |
| Skills and Competencies
? Advanced degree in pharmacy, pharmacology or other life sciences or equivalent experience in the therapeutic area
? 10+ years experience in regulatory affairs with at least 5 years in review and approval of product promotional material or 15+years relevant pharmaceutical experience
? Comprehensive understanding of relevant promotional regulations and guidances including those relevant to labeling, product promotion and scientific exchange of information
? Working understanding of drug development process
? Significant experience (5 years) interacting with FDA/DDMAC and an understanding of drug development process
? Excellent verbal, written and communication skills with an ability to write and articulate regulatory/scientific arguments in a persuasive manner
? Experience in managing and directing staff
? Demonstrated experience in project management, ability to lead project teams, and manage projects to completion
Preferred
? 1-2 years experience interacting with FDA/OND
? Drug Development experience 1-3 years
? 4-5 years experience in managing and directing staff
? Experience in and understanding of respiratory products
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Director; Managed Markets Govt Portfolio & Rptg |
| ? BS Degree in Accounting or Finance.
? In depth knowledge of EXCEL and working knowledge of other MS Office applications.
? Knowledge of Managed Markets Industry, related systems, and pharmaceutical distribution networks is required.
? Excellent analytical and estimating capabilities, exercises good judgment with less than complete data.
? Excellent communication, interpersonal, and organizational skills.
? Ability to effectively work with cross-functional teams.
? Ability to develop and negotiate equitable audit settlements with AstraZeneca?s largest customers.
? 10+ years related work experience in accounting, audit, or finance/business analysis.
? Experience in the leadership and management of people.
? Experience bringing analytical financial support to operational processes and commercial functions.
? Strategic Thinking Skills
Preferred Background
? Masters degree in a relevant field (e.g., accounting, finance, marketing MBA).
? Certified Internal Auditor (CIA) or a Certified Public Accountant (CPA) designation a plus.
? Experience partnering with senior executives and in preparing and delivering presentations to senior management.
? Ability to insightfully conceptualize, model and discuss complex government policies and commercial pressures facing AstraZeneca in the delivery of its products to the emerging government markets.
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| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Learning Specialist |
| ? Bachelor?s degree, preferably in a learning and development or related field (e.g., education, instructional design, instructional technology, human performance improvement (HPI), organization design) with 5 or more years experience in a pharmaceutical or related field in some aspect of strategic learning management
? Effective communication, presentation, organizational & interpersonal skills.
? Strong understanding of adult learning theory, instructional design and a variety of learning methodologies.
? Demonstrated internal consulting skills and ability to facilitate and provide feedback with employees and leaders at all levels.
? Good project management, problem-solving and decision-making skills.
? Ability to perform well in a team-based environment.
? Ability to align learning initiatives with strategic objectives
Preferred Background
? Bachelor?s degree in a development/training/learning discipline with 5 or more years of management/supervisory experience.
? Involvement in industry groups with specializations in effective learning management and training.
? Working knowledge of cGMP?s and Safety, Health and Environmental regulations or experience working in a regulated environment
? Working knowledge of Lean and 6 sigma
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Manager; Brand Corporate Affairs |
| ? BS/BA degree in Communications, Marketing or a related field
? 5 - 7 years Communications experience
? Effective communicator: written, verbal and presenting to groups
? Experience managing PR agencies and managing $MM+ budgets
? Brand technical knowledge
? Knowledge of the pharmaceutical industry
? Working knowledge and experience with marketing objectives and business strategies
? Demonstrated understanding of and ability to perform effectively and successfully in the industry and in the environment in which it operates.
Skills and Competencies:
? Strong writing skills-both internal and external audiences
? Media relations skills and training
? Project management skills
? Strategic planning and influencing skills
? Strong interpersonal skills and able to build strategic working relationships
? 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
? 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.
? 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:
? Experience with issues management desirable
? Background in public affairs or journalism is preferred
? Healthcare PR or agency experience is preferred
|
| 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
|
| Promotional Regulatory Affairs Reviewer (Assoc Dir/Sr Mgr) - 2 Positions |
| Minimum:
? Degree in pharmacy, pharmacology or other life sciences or equivalent experience
? 5+ years experience in regulatory affairs with at least 2 years in review and approval of product promotional material or 10+ years relevant pharmaceutical experience
? Working understanding of relevant promotional regulations and guidances including labeling, product promotion and scientific exchange of information
? Experience interacting with FDA/DDMAC (1-3 years)
? Demonstrated ability to review product promotional material, identify false and misleading information, and propose alternate solutions to mitigate risks
? Ability to lead and facilitate team meetings and managing/resolving conflict
? Experience working in a team-based environment
? Excellent verbal, written and communication skills and ability to write and articulate persuasive scientific/regulatory arguments
? Experience in project management
? Demonstrated proficiency in the following competencies: ethics, standards, attention to detail
Preferred:
? Direct experience interacting with FDA (1-2 years; Review Division)
? Understanding of drug development process
? Pharmaceutical marketing or commercial experience
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Promotional Regulatory Affairs Reviewer (Assoc Dir/Sr Mgr) - Part-time |
| Minimum:
? Degree in pharmacy, pharmacology or other life sciences or equivalent experience
? 5+ years experience in regulatory affairs with at least 2 years in review and approval of product promotional material or 10+ years relevant pharmaceutical experience
? Working understanding of relevant promotional regulations and guidances including labeling, product promotion and scientific exchange of information
? Experience interacting with FDA/DDMAC (1-3 years)
? Demonstrated ability to review product promotional material, identify false and misleading information, and propose alternate solutions to mitigate risks
? Ability to lead and facilitate team meetings and managing/resolving conflict
? Experience working in a team-based environment
? Excellent verbal, written and communication skills and ability to write and articulate persuasive scientific/regulatory arguments
? Experience in project management
? Demonstrated proficiency in the following competencies: ethics, standards, attention to detail
Preferred:
? Direct experience interacting with FDA (1-2 years; Review Division)
? Understanding of drug development process
? Pharmaceutical marketing or commercial experience
|
| 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
|
| Senior Medical Information Manager |
| ? Advanced degree in Pharmacy (PharmD preferred), Pharmacology, Science or equivalent clinical experience
? Pharmacy Licensure preferred
? 2+ years experience in pharmaceutical industry based Drug Information Delivery or equivalent industry experience
? Demonstrated expertise in drug information communication and management
? Excellent oral and written communication skills and interpersonal skills
? Knowledge of FDA requirements
? Ability to apply Regulatory and Compliance guidelines to Drug Information delivery
? Understanding of the information needs for various customer segments
? Project Management leadership experience
? Strong leadership ability
Preferred Background
? Clinical Pharmacy experience with patient care exposure
? Drug Information Residency or equivalent experience
Skills and Competencies
? Expert Scientific Knowledge
? Leadership Skills
? Drug Information Management Expertise
? Regulatory and Compliance Expertise
? Organization Savvy
? Communication Skills
? Presentation, Facilitation and Instructional Skills
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Glbl Ops Assoc - Engineering |
| So what does it take?
First and foremost, we?re looking for people who can quickly understand the Operations environment. In addition, it?s crucial you have strong business acumen, plus the ability to lead teams as well as delivering operational strategies through suppliers and delivering for our customers. A degree in a relevant discipline and a valid passport are essential. You will also need to be geographically mobile and be comfortable spending time working and living overseas.
Minimum Qualifications:
? Minimum requirement of a Bachelors degree in the field of Engineering
? GPA of 3.0 or higher
Preferred Qualifications:
? Demonstrated Leadership experience in work, education or organizational membership experiences
? This program is designed for entry level experience and candidates preferred for these positions have 0-to-3 years of work experience.
? As we are a Global organization, you will also need to be fluent in English. Additional language skills are desirable, especially Mandarin or Chinese, Swedish, Spanish or another European language.
Success factors
? You will have the ability and desire to develop
o Broad functional and business awareness
o Strong commercial and strategic acumen
o Leadership and change management capabilities
o Global cultural awareness and influencing skills
? You feel stimulated to work with pharmaceuticals and health.
? You have the desire to make a difference and a drive to deliver maximum value
Please apply as soon as possible since we are working on an ongoing basis with the selection process.
|
| 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
|
| Glbl Ops Assoc - Procurement |
| First and foremost, we?re looking for people who can quickly understand the Operations environment. In addition, it?s crucial you have strong business acumen, plus the ability to lead teams as well as delivering operational strategies through suppliers and delivering for our customers. A degree in a relevant discipline and a valid passport are essential. You will also need to be geographically mobile and be comfortable spending time working and living overseas.
Minimum Qualifications:
? Minimum requirement of a Bachelors degree in the field of business, management, finance or other relevant field
? GPA of 3.0 or higher
? Geographically mobile-comfortable spending time and working overseas
? Strong business acumen
? Proficiency in Microsoft Suite
? Ability to manage multiple projects/tasks effectively
? Team player with strong analytical skills
? Self-motivated and strong communication skills
Preferred Qualifications:
? Demonstrated Leadership experience in work, education or organizational membership experiences
? This program is designed for entry level experience and candidates preferred for these positions have 0-to-3 years of work experience.
? As we are a Global organization, you will also need to be fluent in English. Additional language skills are desirable, especially Mandarin or Chinese, Swedish or another European language.
? Solid understanding of Lean / 6 sigma concepts, principles and tools as applied to the business as a whole (not just Lean manufacturing)
? Solid understanding of Pharma supply chain, processes and GxP requirements
? Understanding of policies and procedures relevant to his/her area
? Financial awareness
? Corporate responsibility
? Understanding of SHE standards and the impact of change on SHE
? Works effectively with technology
Success factors
? You will have the ability and desire to develop
o Broad functional and business awareness
o Strong commercial and strategic acumen
o Leadership and change management capabilities
o Global cultural awareness and influencing skills
? You feel stimulated to work with pharmaceuticals and health.
? You have the desire to make a difference and a drive to deliver maximum value
Please apply as soon as possible since we are working on an ongoing basis with the selection process.
|
| 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 |
Boston |
MA |
11/19/2009
|
| Prin Sci; In Vivo Cancer Pharmacology |
| Ph.D. with a minimum of 5 years industry experience in Pharmacology.
Competencies
Strong in vivo pharmacology skills in cancer drug discovery.
Direct experience working with in vivo models of cancer such as xenograft, syngeneic and orthotopic models
Understanding of drug discovery and development process
Strong communication skills
Interpersonal skills and the ability to work across project teams
Ability to manage multiple tasks
Effective leadership skills
Strong management skills
Behaviours
Is delivery focused
Is candid and honest in discussions
Demonstrates flexibility, open-mindedness and adaptability
Team working
|
| 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 |
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 |
Warsaw |
IN |
11/19/2009
|
| Senior Clinical Research Associate (in-house) |
| A minimum of a BS/BA or equivalent with 5 years clinical research experience, or a minimum 3 years experience with advanced technical degree. Advanced degree preferred. Certification from recognized professional organization (i.e. ACRP, SoCRA) preferred. Experience in orthopedics and/or orthopedic clinical trials is preferred. Experience monitoring clinical trials is required. A thorough understanding of the clinical trial process and guidelines/regulations associated is required. Experience mentoring and/or training others is preferred. Approximately 25% domestic and international travel is required. |
| 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 |
|
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 |
Somerville |
NJ |
11/19/2009
|
| Regulatory Affairs Specialist |
| A minimum of a Bachelor's degree in Biology, Biochemistry, Immunology or a related discipline is required. A PhD degree in Biology, Biochemistry, Immunology or a related discipline is strongly preferred. A minimum of 2+ years experience in Regulatory Affairs required. Experience or exposure to the field of Biologics is required. Medical Device and Pharmaceutical experience is an asset. US Regulatory experience is required. EU and International Regulatory experience is an asset. Previous experience in regulations and submitting files for health authorities in Israel is an asset. Excellent communication skills will be necessary for this role. This position will require 10% travel and will be located in Somerville, NJ. |
| Johnson & Johnson Family of Companies |
Fort Washington |
PA |
11/19/2009
|
| Associate Director, Medical Affairs - Pain Innovation |
| A life science doctoral degree (MD, DO, PhD, PharmD) is required. For healthcare providers, an active unrestricted license to practice medicine is preferred. For physicians, board certification (or equivalent) is desirable. Certification in rheumatology and/or pain management is preferable. Patient care experience is required. Pharmaceutical experience and/or exposure to clinical research in an academic setting is preferred. Complimentary or alternative pain therapies experience is preferred. Clinical research and development experience, especially experience working with pain medicines and products is preferable. Expertise in pharmaceutical new product and claims development including line extensions and Rx-to-OTC switches is preferred? Strong leadership and interpersonal skills are required. Motivated, self-starting team player with the leadership qualities needed to participate on global cross-functional teams is required. Analytical and presentation skills that facilitate translating scientific/medical/technical concepts to non-scientists clearly and concisely is required. Strong oral and written English skills are required. This position is based in Fort Washington, PA and requires 10% domestic and international 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 |
Fort Washington |
PA |
11/19/2009
|
| Associate Director, Medical Affairs - Upper Respiratory Innovation |
| A life science doctoral degree (MD, DO, PhD, PharmD) is required. For healthcare providers, an active unrestricted license to practice medicine is preferred. For physicians, board certification (or equivalent) is desirable. Certification in allergy/clinical immunology, otolaryngology or pulmonary is preferable. Patient care experience is required. Pharmaceutical experience and/or exposure to clinical research in an academic setting is preferred. Clinical research and development experience, especially experience working with upper respiratory medicines and products or complimentary or alternative therapies is preferable. Expertise in pharmaceutical new product and claims development including line extensions and Rx-to-OTC switches is preferred. Strong leadership and interpersonal skills are required. Motivated, self-starting team player with the leadership qualities needed to participate on global cross-functional teams is required. Analytical and presentation skills that facilitate translating scientific/medical/technical concepts to non-scientists clearly and concisely is required. Strong oral and written English skills are required. This position is based in Fort Washington, PA and requires 10% domestic and international 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 |
Wilkes Barre |
PA |
11/19/2009
|
| Scranton, PA: Sales Representative: J&J Wound Management: Biosurgicals, Unit of ETHICON, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, minimum of two years outside selling experience, the ability to travel as necessary (potentially overnight and/or weekend) is required. Must have a valid driver's license and clean driving record; and, excellent written and oral communication skills. Would prefer candidates with documented successful sales performance (high growth, results vs. plan), ability to target accounts and achieve results through a daily action plan; and ability to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributor reps) and KOLs. Self-starters with strong time management and planning skills are a plus. Hospital-based pharmaceutical or medical device experience as well as experience in product sales to a highly educated/high profile customer base is strongly preferred, but not required. Preference will be given to those individuals living within 30 miles of the posted territory. 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 |
Frederick |
MD |
11/19/2009
|
| Central, MD - Sales Representative - Vistakon, Division of Johnson & Johnson Vision Care, Inc. |
| To be considered for this role, the candidate must have at least a Bachelor's Degree, coupled with at least 3 years of business-to-business and/or medical sales experience. Candidates must have a valid driver's license issued in one of the 50 States and a clean driving record. The ability to travel as necessary, which may include overnight and/or weekend travel is required. Candidates must also have excellent written and oral communication skills. Preference will be given to candidates with documented sales awards and achievements, prior management development training and/or have taken career development classes or completion of a major sales training course. Preference will also be given to candidates living within 30 miles of the posted territory. 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 |
St. Louis |
MO |
11/19/2009
|
| St. Louis, MO (East): Sales Representative: Women's Health & Urology, Unit of ETHICON, Inc. |
| A minimum of a Bachelor's degree is required. A minimum of two years of outside selling experience is also required. Excellent written and oral communication skills are essential. Candidates must have a valid driver's license issued in one of the 50 United States and a 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 (ie. high growth, results vs. plan). The ideal candidate will 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, etc.), external companies, and key opinion leaders. Medical device sales experience, in an operating room environment, 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 |
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 Mechanical Engineer |
| A minimum of a Bachelor's degree in Mechanical Engineering, Design Engineering, Biomedical Engineering or a related discipline is required. An advanced degree is an asset. A minimum of 2+ years work experience in product design/development or manufacturing processes testing is required. Experience in design and development of medical devices is an asset. Experience in design of mechanical devices, systems and/or electro-mechanical products is an asset. Successful completion of products from concept to launch is an asset. CAD ability in Solidworks, Mechanical Desktop or equivalent design software is an asset. A general knowledge and understanding of QSR, DOE, QFD, DFMA, and FMEA is an asset. Must be able to apply and comprehend a broad range of engineering and scientific assignments as well as have demonstrated the ability to work independently and within a group. Will utilize the support of technicians also assigned to the project team. Computer literate in project planning and or data acquisition is desirable. Must be self-motivating and innovative and be able to work on multiple projects with different priorities. Extensive verbal and technical writing skills as well as proven analytical and problem solving 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 Engineer |
| A minimum of a Bachelor's degree in an Engineering discipline is required. An advanced degree is an asset. A minimum of 5 years of related engineering experience in an FDA regulated environment is required. Knowledge of ISO and cGMP regulations is required. Previous experience with conducting design verification and validation testing in support regulatory submissions required. Experience with competitive benchmarking, and process qualifications is required. Engineering prototype evaluation is an asset. Project management experience required. Strong communication, and influencing skills are required. A certification in Process Excellence (Green Belt or Black Belt) is an asset. This position may require up to 25% domestic and international 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 |
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 |
|
PA |
11/19/2009
|
| Director, Medical Affairs Strategic Trials Team (Horsham, PA) |
| MD/DO or PhD with advanced management training or experience is required, preferably in Gastroenterology, Rheumatology or Dermatology. A minimum of 5 years of clinical and managerial experience in pharmaceutical trial design and conduct (Phase II-IV) is strongly preferred. Significant experience in supervising and managing clinical research programs is required. Excellent interpersonal and public speaking skills are required for this high visibility position. Demonstrated ability to work in a matrix type environment with interaction with cross-functional teams. Up to 10% travel (domestic and international) is 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 |
Phoenix |
AZ |
11/19/2009
|
| CLINICAL EDUC SPEC ULTRASOUND Phoenix, AZ |
| A minimum of 3 years clinical experience in echocardiography is required. Registered Diagnostic Cardiac Sonographer (RDCS) or Registered Cardiac Sonographer (RCS) certification or eligibility to sit for certification is required.. Excellent presentation and training skills; outstanding interpersonal and relationship-building Bachelor's Degree (or equivalent), RN, PA-C, CNP is required. Solid organizational and time management abilities required as this is a field-based position. Ability to travel up to 75% of the time in the region is required. Ability to wear protective lead in the lab is required. A valid US driver license and clean driving record 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 |
Memphis |
TN |
11/19/2009
|
| Memphis, TN: Sales Representative: Women's Health & Urology, Unit of ETHICON, Inc. |
| A minimum of a Bachelor's degree is required. A miniumm of two years of outside selling experience, excellent written and oral communication skills are also required. A valid driver's license issued in one of the 50 States and clean driving record is required. 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 |
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 |
Cincinnati |
OH |
11/19/2009
|
| Principal Scientist Veterinary Surgeon - Cincinnati, OH |
| A minimum of a DVM from an AVMA (American Veterinary Medical Association) approved and accredited program is required. (Board Certification is strongly preferred but not required.) A Master's and/or PhD is preferred. Advanced training including veterinary surgical residency is also preferred. A minimum of 3 years of overall research/surgical experience is required. Veterinary surgery experience utilizing veterinary models is required. Preclinical study model design experience is required. Experience as a Study Director/Leader for product evaluations is strongly preferred. Medical Device development experience is preferred. Small animal and soft tissue experience is preferred. Experience working with cross-functional groups/teams is preferred. Leadership experience/ability is strongly 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 |
Phoenix |
AZ |
11/19/2009
|
| Southwest Region: Account Manager : Therakos, Inc. a Johnson & Johnson Medical Device Company |
| To be considered for this role, candidates must meet the following criteria: Undergraduate degree required; Life Science or Science background preferred. Three to Five years of sales experience is required. Five + years of sales experience is preferred. You will need to demonstrate a record of accomplishments. Biopharmaceutical and/or Medical capital equipment sales experience preferred. |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Regulatory Affairs Specialist |
| A minimum of a Bachelor's degree in Biology, Biochemistry, Immunology or a related discipline is required. A PhD degree in Biology, Biochemistry, Immunology or a related discipline is strongly preferred. A minimum of 2+ years experience in Regulatory Affairs required. Experience or exposure to the field of Biologics is required. Medical Device and Pharmaceutical experience is an asset. US Regulatory experience is required. EU and International Regulatory experience is an asset. Previous experience in regulations and submitting files for health authorities in Israel is an asset. Excellent communication skills will be necessary for this role. This position will require 10% travel and will be located in Somerville, NJ. |
| 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 |
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 |
|
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 |
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 |
|
PA |
11/19/2009
|
| Principal Research Scientist (Data Warehouse Administrator) - Radnor |
| A minimum of a PhD is required with at least 5 years of experience. Knowledge of biology and/or clinical science in the therapeutic areas of interest (immunology, oncology, etc.) is required. Must have excellent communication skills, demonstrated leadership skills, and the ability to operate in matrixed and global environment. Technical expertise with bioinformatics and/or medical informatics applications is required. Must have experience with database development in commercial setting as well as experience with data mining algorithms and applying them to biological and/or clinical problems. 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 Operations |
| Requires a BS or BA in a relevant scientific discipline and minimum 8 years relevant clinical experience in the pharmaceutical or medical device industry.Excellent interpersonal skills, and demonstrated ability to lead is required.Experience in managing staff as well as mentoring and developing junior staff.Strong communication and influence skills and ability to create a clear sense of direction is necessary. Must have a demonstrated ability to successfully develop, implement, manage and complete clinical trials.Thorough knowledge and understanding of FDA and/or GCPs is required and EMEA Regulations, ICH Guidelines, and governing the conduct of clinical trials is an asset. Experience in developing RFPs and selection and management of CROs/vendors.Ability to examine functional issues from a broader organizational perspective.Ability to participate in and/or lead departmental or interdepartmental strategic initiatives under limited supervision.Ability to meet on time delivery and deadlines and expediting others is a requirement.Functional expertise to initiate, author, or contribute to SOP development, implementation, and trainingIf 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 |
Indianapolis |
IN |
11/19/2009
|
| Indianapolis, IN : Clinical Sales Representative: J&J Wound Management: Biosurgicals, Unit of ETHICON, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, minimum of three years outside selling experience, the ability to travel as necessary (potentially overnight and/or weekend) is required. Must have a valid driver's license and clean driving record; and, excellent written and oral communication skills. Would prefer candidates with documented successful sales performance (high growth, results vs. plan), ability to target accounts and achieve results through a daily action plan; and ability to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributor reps) and KOLs. Self-starters with strong time management and planning skills are a plus. Hospital-based pharmaceutical or medical device experience as well as experience in product sales to a highly educated/high profile customer base is strongly 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 |
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 |
Raynham |
MA |
11/19/2009
|
| Program Manager |
| BS/BA required. A minimum of 2 years experience working in organizational learning, seminar planning or medical education required. Healthcare experience preferred. Must work well in a team environment. Ability to make decisions independently and seek guidance where appropriate required. Proven written and oral communication skills required. Strong time management skills required. Approximately 30% travel required. |
| 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 |
Mountain View |
CA |
11/19/2009
|
| Maintenance Mechanic |
| A minimum of a High School diploma or equivalent is required. Technical training in electrical and / or plumbing is required. Technical training in HVAC is preferred. A minimum of 5 years experience performing facility and manufacturing equipment maintenance is required. Experience troubleshooting and repairing in the medical, electronics or food processing industries is preferred. Experience working in a current Good Manufacturing Practice (cGMP) environment utilizing Standard Operating Procedures (SOPs) or Standard Company Procedures (SCPs) is preferred. Basic computer skills required, including Microsoft Word, Excel, PowerPoint and Outlook. Previous usage of Computer Maintenance Management System (CMMS) is required. Experience using CAD and/or Visio is preferred. Knowledge of local and national electrical, plumbing and building codes is required. Very good oral and written communications skills is required. Ability to follow all safety and clean room requirements is required. The physical requirements of this position require heavy lifting (up to 80 lbs). This will be a first shift position between the hours of 6:00 am and 5:00 pm, with overtime, weekend and holidays, as needed by business. This position will require rotating on-call duties for any emergencies or alarms during off hours and weekends. This position will be based in Mountain View, 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 |
Raynham |
MA |
11/19/2009
|
| Mechanic II, Production Maintenance |
| A minimum of a High School diploma, G.E.D. or equivalent required. Technical school preferred. A minimum of 4 years of related equipment maintenance experience and/or training is required. Experience maintaining CNC Mills, Lathes, Grinders, EDMs (Electrical Discharge Machines) and ABB Robotics required. Experience maintaining Fanuc and Siemens CNC controllers preferred. Experience maintaining mechanical, electrical/electronic, hydraulic and pneumatic equipment components required. Basic computer skills required. Must be a certified Forklift and Power Pallet Jack Operator or be willing to become certified. Must be able to supply own hand tools (i.e. screw drivers, socket wrenches, etc.). Must be able to communicate (read, write and speak) effectively in English. Must have strong communication and interpersonal skills. The ability to left heavy loads, stand and/or walk more than 90% of the time and perform twisting and turning activities required. The ability to work in confined or awkward areas, climb ladders and work from heights required. Must have a valid driver's license. Must be a team player and be able to work with minimal technical supervision. Must be able to work 2nd shift (3:30 pm - 12:00 am). This ability to work overtime, including weekends, and to participate in on-call rotation is required. This position requires the incumbent to submit to and pass periodic and random drug testing as a condition of initial and continued employment. 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
|
| 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 |
|
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 |
Somerville |
NJ |
11/19/2009
|
| Truck Driver/Distribution Operator |
| A minimum of a High school diploma, G.E.D. or equivalent required. A minimum of a NJ state issued Class B Commercial Drivers License (CDL) is required. Experience operating a vehicle rated 26,000 lbs. or greater is required. A minimum of 3 year of experience driving a truck with CDL accreditation required. Experience in a warehousing operation environment preferred. Experience working in a Good Manufacturing Practice (GMP) or other regulated environment preferred. Basic math skills required. Basic computer skills required. Must have excellent communication and interpersonal skills. Must be detail-oriented and demonstrate alertness, accuracy and patience. Must follow good driving procedures and be highly safety conscious. Experience performing basic vehicle service is preferred. The ability to drive and handle a large panel truck on open highways and in congested areas required. The ability to operate a manual and motorized pallet/hand truck required. The ability to lift/carry up to 35 pounds unaided is required. The ability to work occasional overtime 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 |
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 |
Somerville |
NJ |
11/19/2009
|
| SENIOR DIRECTOR, REGULATORY AFFAIRS |
| A minimum of a Bachelor's degree in a scientific discipline is required, with an advanced degree is strongly preferred. A minimum 10+ years of experience in regulatory affairs or a related field is required. RAC is an asset. Direct experience with US/EU regulatory submissions is required. PMA experience or experience with PMA products is an asset. Experience successfully taking a product through development and regulatory cycle required. Proven leadership and strong people management skills will be needed. Successful track record in coordinating and experience with interacting with multiple and diverse business units required. Excellent oral and written communication skills 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 |
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 |
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 |
Buffalo |
NY |
11/19/2009
|
| Buffalo/Rochester, NY: Sales Representative: Women's Health & Urology, Unit of ETHICON, Inc. |
| A minimum of a Bachelor's degree is required. A minimum of two years of outside selling experience is also required. Excellent written and oral communication skills are essential. Candidates must have a valid driver's license issued in one of the 50 United States and a 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 (ie. high growth, results vs. plan). The ideal candidate will 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, etc.), external companies, and key opinion leaders. Medical device sales experience, in an operating room environment, 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 |
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
|
| Manager, Regulatory Affairs |
| A minimum of Bachelor's degree in a technical, scientific, or medical/health discipline is required. An advanced degree is an asset. A minimum of 8+ years experience in a regulated healthcare industry is required. Direct experience in Regulatory Affairs is required. Experience with or exposure to 510(k) submissions is required. US regulations knowledge is required, with EU and International/OUS experience an asset. PMA experience is an asset. Copy review experience is an asset. RAC is an asset. Excellent verbal and written communication skills will be needed. The ability to influence and negotiate with business partners and regulatory agencies will be required. This position will be 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 |
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 |
Raritan |
NJ |
11/19/2009
|
| I/T SOX PROGRAM MANAGER |
| Experience in design and implementation of COBIT framework for SOX and Assessment within large, complex IT environments. Preferred experience with implementation in Fortune 500 Company.Bachelor's degree required. Advanced degree preferred. 10+years business experience required; 5+ years IT Compliance, information security, and/or audit experience in Big4 environment required.Subject matter expertise in SOX Compliance and Controls with experience interfacing with various auditing/regulatory entities required.External SOX IT Audit experience required.Experience performing "top-down" IT Risk Assessments for systems impacting internal controls over financial reporting. Experience in Risk ManagementExperience training and educating audit staff and control owners on SOX compliance requirements.Experience writing policies and managing compliance documents.Knowledge of IT systems and process analysis tools.Awareness of common security technologies.Demonstrated management skills building and motivating teams in an environment undergoing high amounts of change. |
| Johnson & Johnson Family of Companies |
West Chester |
PA |
11/19/2009
|
| DIRECTOR BILLING & CONTRACT COMPLIANCE |
| BA/BS degree is required, advanced degree is preferred. A minimum of ten years overall business experience with five years in biopharmaceutical, pharmaceutical, or medical device industry is required. Experience working with or familiar with DME Supplier standards is required. Experience working in government/commercial compliance, contracting including but not limited to operational experience in impact analysis and strategic overlays (Pharmaceutical, Device and/or Consumer) and timely/accurate remediation and adjudication, law or related area is required. Experience supervising projects using internal and/or external resources within a matrix environment is required. Demonstrated experience with HCC and GCC programs is required. Health Care Compliance certifications are preferred. This position will be based in West Chester, Pa and will require 15% travel. Due to technical upgrades, this requisition is replacing requisition #0903460. Any candidates who have already applied to requisition #0903460 are already being considered, therefore, you do not need to apply. 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 |
Athens |
GA |
11/19/2009
|
| MANAGER, ANALYTICAL SERVICES |
| Minimum requirements include BS/MS with 7+ years of related experience in an Analytical Laboratory; or Ph.D. with 4+ years of related experience in an Analytical Laboratory; or an equivalent combination of education and experience. |
| Johnson & Johnson Family of Companies |
Chicago |
IL |
11/19/2009
|
| Chicago, IL / Detroit, MI : Account Manager: Therakos, Inc. a Johnson & Johnson Medical Device Company |
| To be considered for this role, candidates must meet the following criteria: Undergraduate degree required; Life Science or Science background preferred. Three to Five years of sales experience is required. Five + years of sales experience is preferred. You will need to demonstrate a record of accomplishments. Biopharmaceutical and/or Medical capital equipment sales experience preferred. |
| 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 |
South San Francisco |
CA |
11/19/2009
|
| Manager, Information Technology and Facilities Management - Janssen Al, LLC |
| A minimum of a High School Diploma is required, a Bachelors degree is preferred. Project Management Professional (PMP) Qualification is preferred. Experienced in I.T. support for Facilities/Operations groups is required. Experienced in I.T. and Facilities change management with a in Pharma R&D organization is required. Experience with administration and coordination skills across peer groups is required. Knowledge of J&J systems, J&J standards and processes is preferred. 10-20% International and Domestic travel is required. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Manager of Financial Reporting and Analysis - Janssen AI, LLC |
| A minimum of a Bachelors Degree in Finance or Accounting. A minimum of 5 years financial experience required. Experience working within a pharmaceutical industry experience preferred. Excellent PC skills and experience including SAP, Excel and PowerPoint. Strong analytical ability. Exceptional communication and interpersonal skills, including oral and written. Demonstrated ability to perform in an environment that emphasizes teamwork. Demonstrated ability to lead a process with minimal or no supervision. Demonstrated capacity to effectively manage multiple and frequently changing priorities. High degree of accuracy with attention to detail and ability to meet strict deadline. 10% Domestic and International Travel is required. |
| Johnson & Johnson Family of Companies |
New York |
NY |
11/19/2009
|
| New York/New Jersey: Account Manager: Therakos, Inc. a Johnson & Johnson Medical Device Company |
| To be considered for this role, candidates must meet the following criteria: Undergraduate degree required; Life Science or Science background preferred. Three to Five years of sales experience is required. Five + years of sales experience is preferred. You will need to demonstrate a record of accomplishments. Biopharmaceutical and/or Medical capital equipment sales experience preferred. |
| 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 |
Rochester |
NY |
11/19/2009
|
| Rochester, NY/Syracuse, NY/Buffalo, NY: Territory Manager (Electrophysiology) - Biosense Webster |
| To be considered for this role, the candidates must meet the following criteria: at least a Bachelor's Degree, MBA preferred. This must be coupled with at least 3 - 5 years of medical device sales experience. Candidates must have a valid driver's license issued in one of the 50 States and a clean driving record. Ability to travel as necessary, which may include overnight and/or weekend travel is required. Candidates must have excellent written and oral communication skills. Ability to work within a commission driven position with the ability to meet and exceed sales goals is required. Preference will be given to candidates with medical device sales experience in the cardiology/cardiovascular medical device industry, preferably with EP experience. Candidates with documented sales 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 |
South San Francisco |
CA |
11/19/2009
|
| Strategic Marketing Director- Janssen AI, LLC |
| Bachelors Degree is required, MBA or Masters Level degree is preferred. A minimum of 10 years of progressive marketing experience in the pharmaceutical industry is required. Launch experience with a pharmaceutical or bio-pharmaceutical product, or experience in a lead role managing a marketed pharmaceutical or bio-pharmaceutical product is also required. Experience in strategic marketing, market development and new product/drug development processes are required. Extensive knowledge of clinical and regulatory development desired. Experience partnering with pharmaceutical R&D teams is required. Strong analytical skills in uncovering and analyzing problem areas/growth opportunities are required. Excellent and proven collaborative skills in developing relationships, leading highly matrixed, high performing, multi-functional cross-company teams, are required. A proven ability to create alignment across teams from multiple operating units, functions and geographies is required. Global experience is preferred. Approximately 20% domestic travel required. |
| 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 |
Jacksonville |
FL |
11/19/2009
|
| Project Manager - Regulatory Submissions |
| A minimum of a Bachelor's degree in a health-related science, information technology, life science or relevant technical or scientific field required. A minimum of 3+ years of direct regulatory experience or information management experience in the pharmaceutical, combination products, consumer/OTC, or related industry is required. A minimum of 2+ years in regulatory operations, specifically with electronic submissions (eCTD) is required. Experience in preparing IND/NDA submissions required. Strong project/submission management experience required. Experience with regulatory processes and standards, including publishing software, document standards and templates and Documentum based documentation management systems required. Working knowledge of Agency regulations and industry standards pertaining to regulatory operations required. Software knowledge in Windows, MS Office, Adobe, XML and SML authoring tools, ISI toolbox, Octagon StartingPoint, Docubridge Publishing Tool, and Labeling Management Systems to support Standard Product Labeling is an asset. Experience publishing clinical study reports according to ICH E3standards for use in eCTD is an asset. Knowledge of GMPs, GLPs, GCPs desirable. An experienced user of the FDA electronic gateway is an asset. Familiarity with life cycle management of electronic submissions is an asset. This position will require 25% 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 |
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 |
Asheville |
NC |
11/19/2009
|
| Asheville, NC- Sales Representative- Women's Health & Urology, a Unit of Ethicon, Inc. |
| A minimum of a Bachelor's degree is required. A minimum of two years of outside selling experience is also required. Excellent written and oral communication skills are essential. Candidates must have a valid driver's license issued in one of the 50 United States and a 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 (ie. high growth, results vs. plan). The ideal candidate will 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, etc.), external companies, and key opinion leaders. Medical device sales experience, in an operating room environment, 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 |
Piscataway |
NJ |
11/19/2009
|
| MANAGER ACUTE CARE CHARGEBACKS |
| A minimum of a Bachelor's degree is required. An MBA is preferred. A minimum of 6 years business experience is required. Strong leadership skills and experience managing people directly or managing cross-functional project teams indirectly is required. Pharmaceutical Chargebacks experience or related experience is required. Knowledge of the contracting continuum is highly preferred. Strong accounting and financial skills are required. Audit skills and experience with developing, implementing and monitoring internal controls is highly preferred. Experience with Sarbanes Oxley, System Implementations and Health Care Compliance is highly desirable. This position will be based in Piscataway and will require up to 15% 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 |
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 |
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 |
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 |
Houston |
TX |
11/19/2009
|
| Houston, TX: Territory Business Manager - Vistakon, Johnson & Johnson Vision Care, Inc. |
| To be considered for this role, the candidate must have at least a Bachelor's Degree, coupled with at least 3 years of business-to-business and/or medical sales experience. Candidates must have a valid driver's license issued in one of the 50 States and a clean driving record. The ability to travel as necessary, which may include overnight and/or weekend travel is required. Candidates must also have excellent written and oral communication skills. Preference will be given to candidates with documented sales awards and achievements, prior management development training and/or have taken career development classes or completion of a major sales training course. Preference will also be given to candidates living within 30 miles of the posted territory. 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 |
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 |
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 |
Raynham |
MA |
11/19/2009
|
| Polish Operator Lead |
| A minimum of a High school diploma, G.E.D. or equivalent required. Vocational designation or training in preferred. A minimum of 3 years of experience working in a machine shop or production line environment, machining precise finished products required. A minimum of 1 year of grinding and/or buffing experience preferred. Experience working in a Medical Device manufacturing environment preferred. Experience working in a Good Manufacturing Practice (GMP) or other regulated environment preferred. Prior experience in a leadership role (i.e. team lead, group lead) preferred. Training experience preferred. Experience working in an environment that has gone through Lean process changes preferred. The ability to drive change as a change agent in a Lean environment required. Basic mechanical skills required. Prior inspection experience required. Knowledge of blueprint reading and geometric tolerance dimensions preferred. Basic computer skills required. Experience collaborating in a team environment required. Ability to communicate effectively (read, write, and speak) in English is required. Must have strong interpersonal skills to work with people of the production floor. 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 |
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 |
|
IL |
11/19/2009
|
| Chicago, IL : District Business Manager: Vistakon, Division of Johnson & Johnson Vision Care, Inc. |
| To be considered for this role, the candidate must have at least a Bachelor's Degree, coupled with a minimum of 5 - 7 years of outside business-to-business, medical, or pharmaceutical sales experience. A minimum of 2 years experience in sales management or successful completion of a Johnson & Johnson Management Development program is required. Candidates must have a valid driver's license issued in one of the 50 States paired with a clean driving record. The ability to travel as necessary, which may include overnight and/or weekend travel is required. Candidates must also have excellent written and oral communication skills and a thorough knowledge and understanding of sales applications and principles. Preference will be given to candidates with documented sales awards and achievements and to candidates with prior ophthalmic healthcare selling experience. |
| 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 |
New Brunswick |
NJ |
11/19/2009
|
| PAYROLL TAX ANALYST |
| Minimum of a Bachelors Degree is required, prefer a major in Finance/Accounting or Business Administration. Minimum of two years payroll or finance related experience is required.Knowledge of country payroll and tax filing requirements (for at least one of the countries this role supports) is required. Experience in the countries preferred (and several languages, as appropriate). Outsourced payroll experience preferred. This role requires the ability to influence others, identify problems and recommend course of action is required. Experience with Microsoft Office Tools is required. Experience with SAP a plus. Demonstrated ability to respond promptly, thoughtfully and effectively to changing work environments, changing priorities, and new situations and excellent organizational skills as well as oral and written communication skills are required for this role. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Clinical Program Manager - Janssen AI, LLC |
| BS or BA in a relevant scientific discipline is required. Must possess at least 5 years of relevant clinical experience in the pharmaceutical (or similar) industry. Excellent interpersonal skills and demonstrated ability to lead is required. Experience in managing staff as well as mentoring and developing junior staff is preferred. Strong communication and influence skills and the ability to create a clear sense of direction is necessary. Must be able to resolve problems using national and international regulations and guidelines. Must have a demonstrated ability to successfully develop, implement, manage and complete clinical trials. Thorough knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is required. Experience in developing RFPs and selection and management of CROs/vendors is required. The ability to write study protocols, study reports, sections for investigator brochures and regulatory documents (e.g. IND, DNA, etc.) with little supervision is required. The ability to examine functional issues from a broader organizational perspective is required. The ability to participate in and/or lead departmental or interdepartmental strategic initiatives under limited supervision is required. Functional expertise to initiate, author, and/or contribute to SOP development, implementation and/or training is preferred. 25% travel is required, both international and domestic. |
| 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 |
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 |
Piscataway |
NJ |
11/19/2009
|
| Customer Contact Center Associate (Casual Part-Time) (1 of 6 Positions) |
| A minimum of a High School Diploma is required. An Associate's Degree is preferred. A minimum of 3 years of experience a fast-paced, complex Customer Service environment (i.e. Accounts Receivable, Transportation, Call Center, Distribution and/or Collections experience) is required. A minimum of 3 years of experience in a health-related service industry is preferred. Must have excellent oral and written communication skills to share information and achieve business results in a respectful and professional manner. Ability to work in a fast paced/ high volume environment with minimal supervision is required. Must have excellent time management and organizational skills and the ability to effectively prioritize. Must have strong teamwork and problem solving skills. Experience with Call Center Management tools, Web Based Order Management Systems and/or SAP is preferred. Knowledge of Microsoft Office products (Excel, Word, Outlook, etc.) is required. Knowledge of Customer Service standards, Medical Products, and following policies, procedures and SOPs is preferred. The qualified candidate will be required to work a part-time shift between the hours of 8:30 AM and 8:00 PM, Monday to Friday totaling a 19.5 hours per week with overtime, weekends and holidays as need by business. This position may require up to 5% domestic travel. Must be willing and able to work in Piscataway, 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 |
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 |
South San Francisco |
CA |
11/19/2009
|
| Global Marketing Director, Infrastructure - Janssen AI, LLC |
| BA/BS required; Advanced degree in business or life sciences preferred. A minimum of 10 years of progressive marketing experience is required with a proven track record of exceptional team & cross-functional leadership. Pharmaceutical industry experience is highly preferred, significant line marketing experience with senior brand responsibility, is required. Global marketing experience and launch experience is preferred. Demonstrated global mindset with the ability to assimilate complex science quickly is required. This position requires up to 25% domestic/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! |
| Johnson & Johnson Family of Companies |
Los Angeles |
CA |
11/19/2009
|
| Manager Drug Safety & Pharmacovigilance (Cougar Biotechnology) |
| A minimum of a Bachelors degree (science or medical related degree preferred) or RN is required; Masters or Doctoral degree in the sciences is preferred. A minimum of 3+ years of biotech/pharmaceutical industry experience in a drug safety role is required. Previous experience writing narratives for serious adverse events (SAEs) is highly preferred. Previous experience with adverse event reporting systems, FDA and EU drug safety/Pharmacovigilance requirements is preferred. Previous experience using ARISg, MedDRA dictionary, and WHO dictionary is highly preferred. Excellent communication, interpersonal, presentation, and facilitation skills are required. Proven ability to evaluate, interpret and present clinical data required. Ability to lead, manage and balance multiple projects and priorities in a dynamic environment required. Up to 25%domestic travel may be 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! |
| Millennium Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Project Manager, Meeting Planning |
|
| Millennium Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Clinical Research Manager II |
|
| 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
|
| Dir, Regulatory Affairs |
|
| Millennium Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Clinical Program Manager |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| QA Specialist II/III, Computer Validation |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Associate Director, CMC Regulatory |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Medical Director |
|
| Millennium Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Sr. Manager, Clinical Operations |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Clinical Research Manager I |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Clinical Research Manager I |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Counsel, Pharmaceutical Marketing & Sales Promotions |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr. Manager, Regulatory CMC |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr Mgr, Regulatory Affairs |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| MGR II, REGULATORY AFFAIRS |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Dir, Regulatory Affairs |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Assoc Director - Solid Formulations |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Associate Director, Regulatory CMC |
|
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Medical Director |
| - Excellent oral and written communication skills.
- Working knowledge of biostatistics, clinical pharmacology and pharmacokinetics.
- Complete understanding of the drug development process.
- Keeps abreast of all regulatory updates and changes and disseminates information effectively and appropriately.
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
|
| Temp. Clinical Project Manager |
| PREFERRED EDUCATION AND EXPERIENCE:
M.S. (or equivalent experience) and 4+ years of relevant work experience
B.S. (or equivalent experience) and 6+ years of relevant work experience
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Stability Manager |
| A Bachelor's Degree and 8 year of Quality Control experience with emphasis on stability program management or equivalent is needed.
Required experience and/or qualifications:
? Management of complex projects
? Working knowledge of trend analysis software is necessary.
? Thorough understanding of cGMP and ICH guidelines
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
|
| Temporary Administrative Associate |
| H.S Diplmoa, A.A. or A.S. and 4-8 years relevant work experience, or B.A. (or equivalent degree) and 3-6 years of relevant work experience. Must have Lotus Notes experience.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Stock Plan Administrator |
| Minimum Education Requirements:
Bachelor's Degree and at least 2-3 years of experience as a stock plan administrator experience.
Required experience and/or qualifications:
This individual will have excellent communication skills and the ability work with departments and employees with varying levels of knowledge. In addition this individual must have a proven ability to manage time lines and deliverables. The ideal candidate will display advanced knowledge of equity administration, applicable rules and regulations, industry standards, industry practice. The ideal candidate will have an in- depth working knowledge of the Equity Edge database. Must have knowledge and experience using Equity Edge application. CEP, a plus.
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 |
Cambridge |
MA |
11/19/2009
|
| Clinical Project Manager |
| Skills:
- Strong study management track record showing clear proficiency in clinical project management skills.
- Solid vendor management skills
- Broad understanding of operations including those in related development functions
- Demonstrates detailed understanding of clinical protocol , intended study populations as well as solid overall drug development
- Demonstrates ability to effectively interface with key medical personnel at clinical site(s)
- Demonstrates ability to lead multi-disciplinary teams
- Possesses excellent written and oral communications skills
Educational:
- B.S. (or equivalent experience) and 6+ years of relevant work experience
- M.S. (or equivalent experience) and 4+ 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
|
| Director, Global Brand Marketing, Cystic Fibrosis |
| - Bachelor?s degree required. Advanced business degree or M.B.A. preferred, additional scientific degree would be a plus
- A minimum of 10 + years of marketing experience with several years experience in the pharmaceutical or biotechnology sectors and a strong preference for experience in many if not all of the following areas: specialty product launch, U.S. product launch, global product launch, specialty markets, cystic fibrosis, orphan drugs/products
- A successful track record with brand management, marketing team leadership, and talent management
- Demonstrated expertise in marketing to diverse customer segments including physicians, payers and consumers
- Documented experience in overseeing life cycle management and market development/expansion activities
- An understanding of the managed markets (payers, channels, pricing) environment in the U.S.
- Proven ability to successfully lead/work in a cross functional team setting (clinical, sales, managed markets, regulatory, legal production, R&D, project management)
- Excellent analytical, communication and organizational/planning skills
- Demonstrated ability to create financial and operational objectives across business departments
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 ContractsParalegal |
| Qualified candidates must have a minimum of 1 ? 3 years corporate law experience or larger firm working primarily in contracts, paralegal certification preferred. Must possess high attention to detail, strong work ethic, be able to take initiative, and have excellent time management and follow-through skills. Must also demonstrate solid written and oral communication skills. Paralegal Certificate and BS or higher required (in a science field preferred). Experience with research & development contracts is a plus.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Scientist/ Senior Scientist |
| The competitive candidate will have an MS or PhD in Pharmaceutics, Chemistry, Chemical/Biochemical Engineering, or Biophysics (or equivalent) with a strong mathematical modeling background.
-The ability to work in a highly cross functional team environment is essential, including the ability to communicate at a technical level with members of research, pharmaceutical development, drug metabolism and clinical pharmacology groups. The candidate should have demonstrated the ability to develop complex mathematical models to simulate and analyze compound behavior in clinical and non-clinical systems.
-Previous experience in PK modeling using Gastroplus, WinNonlin and NONMEM is a plus. Several years of industrial experience in Pharmaceutical Development would further distinguish the candidate.
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. Clinical Project Manager |
| PREFERRED EDUCATION AND EXPERIENCE:
M.S. (or equivalent experience) and 4+ years of relevant work experience
B.S. (or equivalent experience) 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, inflammation, autoimmune diseases, cancer, pain and bacterial infection. We are interested in establishing relationships with well qualified talent today for opportunities we plan to open in the future.
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
|
| Director, Health Economics, Outcomes & Value |
| - Bachelor?s degree in the sciences with a preference for a graduate level degree in a related field of study (e.g. PharmD, PhD, MD, MPH)
- Minimum of 6 years of relevant experience in health economics, outcomes and/or pricing functions
- 4+ years of managing or leading project teams is preferred, experience in developing and managing teams and working in cross functional environment is essential
- Health care industry experience and in-depth knowledge of the pharmaceutical business including R&D, clinical and marketing, as well as a good understanding of managed care;
Related therapeutic experience is preferred, specialty pharmacy category (e.g. HIV, MS, Oncology, etc.) experience considered a plus
- Experience in developing innovative communication strategies and tools to support brand and/or disease value propositions is essential. Experience in developing and/ or utilizing HEOV tools is preferred
- Excellent interpersonal skills are required as is the ability to understand and respond to multiple internal and external customer requests and manage conflict constructively with minimal supervisory support required
- Experience in preparing or reviewing materials for drug formularies considered a plus
- Publication experience a plus
- Ability to travel up to 20% of time.
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
|
| Associate Director, Regulatory Affairs |
| M.S. (or equivalent degree) and 6+ years relevant work experience.
B.S. (or equivalent degree) and 8+ years of relevant work experience.
PhD preferred.
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
|
| Principal Medical Writer |
| Ideal applicants possess outstanding written communication skills, a solid understanding of clinical data analysis, advanced knowledge of researching, writing, editing, and reviewing clinical documents, and a strong record of innovative problem-solving. Applicants must exhibit highly developed skills in teamwork, organization, project management, and oversight of contractors. Preferred candidates have a Ph.D. (or equivalent degree) and at least 5 years of relevant work experience, an M.S. and at least 6 years of relevant work experience, or a B.S. and at least 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
|
| Pharmacometrician II |
| Demonstrates a highly advanced understanding of the requirements of the design, conduct, analysis and report writing for regulatory submissions. Exhibits ability to independently interpret and integrate preclinical PK/PD information into the design, conduct and analysis of preclinical, clinical pharmacology and biopharmaceutical studies. Demonstrates a more thorough understanding of drug metabolism and PK/PD principles. Proven ability to conduct and analyze more complex clinical pharmacology studies using various PK/PD software programs. Communicates more effectively in verbal presentations and in writing technical reports. Ph.D. (or equivalent degree) and 2 ? 5 years of relevant work experience, or M.S. (or equivalent degree) and 7+ years of relevant work experience, or B.S. (or equivalent degree) and 10+ 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
|
| Principal Engineer- Life Cycle |
| At the minimum, a Bachelor's degree in computer science or a scientific or business field or 10+ years of equivalent experience is needed. In addition, this candidate must show the ablilty to work with complex projects both individually and in a team. Strong project mgmt experience is also needed.
7-10 years enterprise level infrastructure experience is needed in design and implementing solutions that include the following components: Windows Servers, Linux, Oracle application/data base servers, Load Balancer, Firewalls, and VPNs.
Additional requirements include:
-Experience with developing service level agreements
-Ability to establish effective collaborative working relationships with multiple support groups across the company.
-Excellent verbal and documentation skills.
-Strong sense of accountability, taking ownership over projects and responsibilities and resolving issues proactively
Research, Pharmaceutical & FDA regulated experience is a plus.
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
|
| Director, Patient Advocacy |
| ?Minimum of ten years current and relevant experience in Patient Advocacy, Public Health Policy, Healthcare, Communications, or related field(s);
?Bachelor?s degree required. An advanced degree within public health or public policy is highly desired;
?Demonstrated outstanding strategic planning, communication and presentation skills;
?Ability to travel up to 35%;
?Pharmaceutical sector or non-profit sector and therapeutic area experience preferred;
?A high level of energy and passion toward patients, science and public health;
?Working knowledge and appreciation of the complexities of the drug development process and regulatory requirements;
?Understanding of the patient and caregiver experience in HCV/CF to include screening, diagnosis, treatment, and treatment options preferred;
?Knowledge of the patient advocacy community/individuals in HCV/CF preferred;
?Proven teamwork and collaboration skills, with a demonstrated ability to interact and influence all levels of business;
?Detail-oriented, self-initiating, well-organized and capable of managing multiple projects simultaneously;
?A desire to work in the corporate culture of a highly innovative company aimed at redefining health, and transforming lives with new medicines.
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
|
| Administrative Associate II |
| * Ideal candidate will have a BA/BS or equivalent and 1 - 3 years for administrative experience supporting multiple senior level people.
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
|
| 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
|
| Sr. Staffing Consultant - Customers & Markets |
| - Minimum of 6+ years corporate pharmaceutical sales and commercial recruiting experience, or equivalent, working in a fast-paced matrix organization. Experience in building a pharmaceutical field force from the ground up highly preferred
- Proven track record in finding unique ways of sourcing qualified candidates, cold calling, relationship building and networking, resulting in successful placements of premium talent. Those individuals with a strong network in this area (Sales/C&M) are urged to apply
- Superior selection skills and proficiency in assessing individuals and small teams, in particular having extensive experience in successfully screening and assessing sales professionals
- Knowledge and experience with staffing and sourcing technologies and adherence to established policies and procedures
- Proven ability to develop successful relationships with business partners, staffing team members and entire HR team
- Demonstrated listening, facilitation and communications skills
- Ability to travel for recruitment and networking events
- Ability to work in a fast-paced, changing environment. We are growing rapidly and change is the constant so bring a positive can do attitude
- Results driven, able to demonstrate/quantify success relative to established targets and metrics
- Experienced and political savvy working with different levels within an organization
- Applicants must possess strong organizational, computer and web skills, along with the ability to multi-task and handle sensitive and confidential situations/information
- Ability to demonstrate Vertex?s core values on a day to day basis when working collaboratively with internal and external individuals as well as when building strategy, and executing tasks or initiatives
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
|
| Medical Director, Cystic Fibrosis |
| ? MD, DO or equivalent ex-US medical degree
? 1-2 years of basic or clinical research experience in an academic setting with publications in peer reviewed journals
? 5+ years of experience in Clinical Development in the pharmaceutical industry
? board certification in Internal Medicine or a similar medical specialty
? Excellent communication skills
? Ability to work collaboratively in a team-based matrix management environment with minimal supervision
? Possess a full understanding of applicable US and EU regulations and of the drug development process
? Have a working knowledge of biostatistics and pharmacokinetics
? Experience in filing and defending US IND's or similar ex-US regulatory submissions
Preferred qualifications include sub-specialty training in internal medicine, family practice, pediatrics, pulmonary medicine or allergy.
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 ? 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, Pharmacovigilance Physician |
| MD degree, Pharmaceutical Industry experience in Pharmacovigilance and drug safety for at least five years, Team working, analytical skills, and flexibility are essential for this position. |
| 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
|
| Formulation Development Scientist -- Agensys, Santa Monica, CA |
| ? Ph.D. in a scientific discipline (Biochemistry, Chemical Engineering, or Biochemical Engineering) with 5+ years of relevant experience in the pharmaceutical /biotechnology industries.? Experience in the pharmaceutical industry is preferred in formulation development or related biochemistry related areas of development (e.g. purification, stability, analytical). ? Experience working with monoclonal antibodies and exposure to early phase formulation development activities? Experience with IV formulations as well as formulation development for poorly soluble compounds would be desirable. ? Proven experience managing the scale-up and manufacturing of parenteral dosage forms? Proven ability to apply the principles of the basic sciences, such as physical and organic chemistry, thermodynamics, and materials science, to pre-formulation and formulation development, using a rational, scientific approach.? Supervisory experience preferred. ? Must be highly motivated, have excellent organizational and communication skills, and must be able to work independently and as part of a multi-disciplinary team. |
| 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. |
Santa Monica |
CA |
11/19/2009
|
| Cell Culture Engineer/Associate, Agensys, Santa Monica, CA |
| ? A B.S. or M.S. in biochemistry, biology, biochemical engineering or a related field. ? 1 to 3 years related experience in the biopharmaceutical/biotech industrial ? Prior hands-on experiences in cell culture process development, especially with shake flasks and bioreactors.? Possess good problem solving, organizational, and documentation skills with a strong focus on details? Must have excellent organizational and communication skills? Must be highly motivated, be able to work independently as well as in teams |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Associate Medical Director/Medical Director, Medical Affairs, |
| M.D. degree, Board Certified or Board Eligible in Designated Specialty (preferred) with subject matter expertise in dermatology or ImmunologyThree years clinical or clinical research experience preferredOne year experience in the pharmaceutical industry preferredExcellent communication and presentation skills, strong interpersonal skills.Strong clinical research/medical affairs background, and excellent problem solving abilities.Demonstrate abilities to work effectively in a team environment.Ability to interpret and evaluate clinical data. Leadership skills and ability to effectively manage projects and timelines. Knowledge of pharmaceutical clinical development and ability to effectively apply technical principles, theories, and concepts to clinical drug development. Knowledge of FDA, other regulatory agency and professional requirements, regulations and guidancesAble to work independently on all aspects of assigned projectsExcellent organizational skills |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Associate Medical Director/Medical Director |
| M.D. degree, preferably with training in internal medicine, family practice is helpful.Minimum two to five years pharmaceutical development experience in the pharmaceutical industry or equivalent academic experience.Strong working-knowledge of regulatory procedures and guidelines (preferably US)The candidate must demonstrate an ability to manage multiple studies, and to work independently on assigned projects. Effective team player in a matrixed R&D environmentExcellent presentation and writing skillsExcellent organizational skills |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Associate Director/Director, Toxicology- Agensys, Santa Monica, CA |
| ? Ph.D in toxicology, biochemistry, pharmacology, pharmacokinetics or related sciences; minimum of 10 years of pharmaceutical industry, including 7 years in toxicology and management experience ? Comprehensive knowledge of drug development (non-clinical and clinical) ? Experience with non-clinical CROs ? Knowledge and experience in biopharmaceutics, toxicology, toxicokinetics, ADME and pharmacokinetics with therapeutic antibodies and antibody drug conjugates ? Knowledge of FDA regulations pertaining to non-clinical and clinical drug development. ? Well developed oral and written communication |
| 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
|
| Assistant Director, Advertising and Promotion Review |
| 1. Bachelor's degree in scientific discipline; advanced degree preferred2. At least 8 years previous industry experience; 5 in RA. Scientific knowledge in chemistry, general biological/physical science and ability to apply that knowledge to regulatory issues and product development having technical complexity. 3. Direct advertising and promotional material review experience required.4. Able to communicate effectively and maintain effective working relationships. Must be able to effectively influence peers and others within the organization.5. Proven ability to prioritize and multi-task with minimal supervision based on interactions with project team members.6. Excellent written and verbal communication skills (native and non-native English speakers) with the ability to meet regulatory requirements and standards while maintaining effective relationships.7. Strong organizational skills and high level of attention to detail, with the ability to coordinate multiple large and diverse projects simultaneously |
| 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
|
| Sr. Manager/Assistant Director, CMC |
| ? A M.S. or Ph.D. in Pharmacy, Pharmaceutics, life sciences or Chemistry plus 3-5 years of experience in the pharmaceutical development of investigational drug candidates is required. A B.S. in Pharmacy or Chemistry with additional relevant experience (5-10 years) can be considered. Title and grade will be based degree and experience as well as the degree of fitness to the Essential Job Responsibilities? Experience with multiple aspects of the process development, analytical characterization, process scale-up and/or regulatory registration of biotechnology drug substances proteins or peptides) is required. ? A thorough knowledge of current pharmaceutical and related industry and processes and practices, and the ability to leverage this knowledge to optimize group and departmental processes is essential.? Experience in the management of contract research organizations or collaboration partners is preferred.? Excellent communication and project management skills are required as this position is responsible for the scientific evaluation and coordination of work performed by external organizations. ? The ability to manage multiple projects and to work well within a team environment are also essential. ? An working understanding of GMP requirements and FDA/ICH guidance is required, as well as facility with commonly available computer tools for project management and data evaluation. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Principal Biostatistician |
| Must have a Ph.D. with at least 4 years experience in applying statistical methods in drug development or a related-area, or have a M.S. with at least 6 years experience in a related area (including 2-3 years in drug development). The incumbent should be well-versed in the clinical guidelines for presentation of the results of experimental data and have a thorough knowledge of how to apply SAS and other statistical software to analyze experimental data. The incumbent should also have excellent oral and written communication skills, in addition to excellent team work skills. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Sr. Director, Oncology Global Strategic Marketing, Product & Portfolio Strategy |
| ? Minimum 7-10 years of pharmaceutical/life sciences experience in, preferably, a strategic marketing, new product development, business development, or similar role? MBA or advanced science degree ? Oncology commercial experience? Global commercial experience? Previous co-promotion experience ? In-depth understanding of the clinical development process |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Senior Director Marketing - Urology |
| REQUIREMENTS:- BA/BS degree with advance degree preferred plus 10-12+ years of relevant experience (depending on degree) required.- Senior directors have an in-depth understanding of multiple, related fields. Ability to set strategy for a department and related company functions. Requires significant communication and leadership skills and the ability to create and implement the department?s mission and integrate it with that of the company?s. - Recognizes problem situations and uses both formal and informal methods to find solutions. Makes independent decisions on the most complex problems. Develops policies that avoid recurrence.- Has responsibility for a major segment of the company. Decisions significantly impact the company?s financial or public relations positioning. Serves as a principal spokesperson for a department or division. - Manages a department consisting of direct reports at the manager and director level.- Establishes and prioritizes area?s project portfolio. Projects usually managed through subordinates and often span across departments and are of major significance. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Director, Marketing - Latin America |
| REQUIREMENTS:- Bachelor's degree in a related discipline with an advanced degree in business or science strongly preferred- 10+ years of relevant experience depending on degree including 5 years marketing leadership experience preferably within the Pharmaceutical industry- Background to include previous supervisory responsibility and international experience preferably in Latin America- Demonstrated ability to manage business within the competitive and regulatory environment.- Requires significant communication and leadership skills and the ability to create and implement the department?s mission and integrate it with the organization?s mission.- Strong relationship management and influencing skills and comfort working with cross-functional teams- Excellent oral and written communication skills. Ability to understand and help define business questions and present findings in a compelling manner to various audience- Must be fluent in Spanish/English with Portuguese highly desirable- Ability to travel domestically and internationally required (up to 50%) |
| 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. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Sr. Administrative Assistant- Agensys, Santa Monica, CA |
| A minimun of 5 years administrative assistant experience including general office coordination responsiblities.A college degree and previous expereince at a biotech, pharmaceutical or healthcare company highly preferred.Strong expertise with Microsoft Office, Oracle and telephone protocol required. Duties require professional verbal and written communication skills and the ability to type 60 wpm. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Sr. Manager Procure to Pay |
| REQUIREMENTS:- BS/BA in Accounting, MBA preferred- Strong knowledge of business processes- Strong knowledge of Financial IT systems- Public accounting experience preferred- Understanding of US Sarbanes-Oxley and on-going compliance requirements.- Expertise in evaluating and implementing process-level business processes- 7+ years working experience in accounting.- 2+ years management experience - Strong verbal and written communication skills a must. |
| 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, 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. |
Rahway |
NJ |
11/19/2009
|
| Research Associate |
| Education requirements:Must currently possess a PhD or expect to earn a PhD within the next 9 months OR must have a Bachelor's or Master's Degree with at least 5 years of research experience and 2 first-author publications. A concentration in one of the following studies is required; mathematics, computational biology, computer science, statistics, or another area applying math, statistics, and/or computer science to biology, biotechnology, chemistry, genetics, biochemistry, or pharmacology. Required: The position requires advanced and thorough scientific knowledge related to the above-mentioned areas of expertise. Must have the ability to plan, recommend and complete research programs of major divisional importance. The incumbent must be capable of motivating and training junior scientists and offering counsel to peers within the Division. Experience in several and extensive knowledge in one or more of the following areas is required: discrete and numerical algorithms, machine learning and automated pattern recognition, signal and/or image processing, computational biology, mathematical analysis and modeling, differential equations, mathematical programming, probability, stochastic processes, scientific software engineering, optimization, parallel algorithms, complexity theory, or knowledge representation. Mature communication and interpersonal skills are required. Preferred: Post-graduate research experience or some combination of directly relevant R&D work and training could also be an asset, especially if relevant to solving problems in the pharmaceutical/biotechnology/biomedical industry. 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 # INF003860. 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 & 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
|
| 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
|
| 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. |
Whitehouse Station |
NJ |
11/19/2009
|
| Co-Op, Graphic Designer- Labeling Services |
| This position requires candidate to be currently in pursuit of a minimum of a Bachelor's degree in graphic arts, package design, or related field. Experience in a pharmaceutical, food, cosmetic labeling or packaging design and development group is a plus. Demonstrated proficiency in the Macintosh Operating System and in graphic arts application software (Creative Suite, including Adobe Acrobat/Distiller, InDesign, and Illustrator) required to produce fully-composed, electronic artwork for printed packaging components (labels, cartons, etc.) is required. Candidate must be able to work full time for a minimum of six months. Successful candidate will display accurate and thorough work. Shows good judgment with thought and detail. Effective communication skills (oral and written) as well as strong organizational skills essential. Strong interpersonal skills and the ability to work well with others and provide significant contributions as a member of a team. Demonstrated flexibility and handle multiple tasks well under pressure. 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 # QUA001917. 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. |
West Point |
PA |
11/19/2009
|
| Merck Manufacturing Business Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Supply Chain Management, Engineering, Business or a related discipline. 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 #ADM003948. 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. |
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
|
| Associate Automation Engineer |
| Education:Must have earned a Bachelor's Degree in Information Technology, Science, Engineering, or related field by December 31st, 2009 or June 30th, 2010. Preferred:A working knowledge of the regulatory requirements for pharmaceutical applications is desirable. Highly desired are skills in PLCs (AB), DCSs (DeltaV / Provox), Batch Operations (S88/S95), IT, and OEM equipment. Merck Location: West Point, Pennsylvania and local satellite offices in Pennsylvania (25 miles northwest of Philadelphia) 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 # ENG002126. 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
|
| Associate Automation Engineer |
| Education:Must have earned a Bachelor's Degree in Information Technology, Science, Engineering, or related field by December 31st, 2009 or June 30th, 2010. Preferred:A working knowledge of the regulatory requirements for pharmaceutical applications is desirable. Highly desired are skills in PLCs (AB), DCSs (DeltaV / Provox), Batch Operations (S88/S95), IT, and OEM equipment. Merck Location: West Point, Pennsylvania and local satellite offices in Pennsylvania (25 miles northwest of Philadelphia) 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 # ENG002127. 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 # 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. |
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. |
Carlow |
L* |
11/19/2009
|
| Process Engineer Technical Operations |
| Education Bsc. in Engineering, Science or similar discipline |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Biometrician |
| Requires a Ph.D. degree in Statistics or Biostatistics. Requires knowledge of statistical methodology, experimental design, and medical background. Requires solid programming expertise including a working knowledge of SAS and S-plus or R. Must be familiar with the basic operation of a computer system, other database processing systems. Must have proof of legal authority to work in the United States. 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 BIO002481. 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
|
| Principal Development Engineer |
| Education:BS, MS or PhD Degree in Chemical Engineering, Materials Engineering/Science or Pharmaceutics with a minimum of 8 years post-bachelors degree experience in Technical Operations, Process Development, or related experience (Ph.D., 4 years or more experience required). Required:At least 3 years of experience in the formulation/development and technology transfer of controlled release dosage forms. Strong Chemical Engineering skills with a desire to perform hands-on work including design and execution of experiments at both pilot scale and during scale up. Thorough understanding of polymer chemistry and other materials along with their impact on drug release. 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 # ENG002042. 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
|
| 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. |
Upper Gwynedd |
PA |
11/19/2009
|
| Director Clinical Research, Oncology |
| · M.D or M.D./Ph.D who is Board Certified or Eligible in Oncology (and Hematology);· Must have experience in industry or academia;· Demonstrated record of scientific scholarship and achievement;· A proven track record in clinical medicine and background in biomedical research is essential;· Prior specific experience in clinical research and prior publication is desirable but not necessary; and· Strong interpersonal skills, as well as the ability to function in a team environment are essential. About MerckConsistently 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 # CLI001839. 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 - MerckSearch 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. |
Carlow |
L* |
11/19/2009
|
| LSS and Change Lead |
| Bachelor's Degree qualification in relevant discipline (Science, Engineering, Business, Operations) Black Belt Qualification |
| 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. |
West Point |
PA |
11/19/2009
|
| Principal Development Engineer |
| Education:BS, MS or PhD Degree in Chemical Engineering or Materials Engineering/Science. Required:A minimum of 8 years post-bachelors degree experience in Manufacturing, Process Development, or acceptable related experience (Ph.D., 4 years or more experience required). Strong Chemical Engineering skills with a desire to perform hands-on work including design and execution of experiments at various scales (lab/ pilot plant etc). 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 # CHE001837. 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. |
Elkton |
VA |
11/19/2009
|
| Safety and Industrial Hygiene Manager |
| Requirements: Bachelor's degree required. Concentrations in Safety, or Industrial Hygiene strongly preferred. Relevant professional certifications and/or Six Sigma Green belt a plus. Minimum of 10 years applied safety professional work experience in a pharmaceutical, chemical or manufacturing environment, coupled with 3 years in a position of safety program leadership. Excellent leadership, program management, project management, and organizational skills. Demonstrated experience in developing facilities to meet OSHA VPP certification criteria or equivalent. Broad based knowledge of safety regulations. Customer focus-team building, proactive style. Excellent verbal and written communication skills. Proven record interpersonal and negotiation skills. Provenience 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 # ENV000115.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. |
Elkton |
VA |
11/19/2009
|
| Sr. Engineer - Sterile Process/Capital Project Support |
| Requirements:Bachelor of Science in Chemical Engineering, Mechanical Engineering, or Biomedical Engineering5 years experience in a process engineering support or capital project engineering role supporting an FDA regulated processPreferred:Experience with a sterile/aseptic processExperience with a pharmaceutical manufacturing process 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 #CHE002167. 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
|
| Staff Engineer - Sterile Process/Capital Project Support |
| Requirements:Bachelor of Science in Chemical Engineering, Mechanical Engineering, or Biomedical Engineering 2 years experience in a process engineering support or capital project engineering role supporting an FDA regulated process Preferred:Experience with a sterile/aseptic process Experience with a pharmaceutical manufacturing process 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 #CHE002165. 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. |
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. |
RTP |
Durham |
11/19/2009
|
| Production Technician |
| Required: HS Diploma/GED 3 years experience in a manufacturing environment with a responsibility for mechanical troubleshooting and repair of automated equipment. Ability to work in a highly effective team environment Strong communication (written/verbal) skills Ability to manage multiple priorities and advance several tasks in parallel Ability to work with and troubleshoot computer control equipment including Programmable Logic Controllers (PLC) and/or Distributed Control Systems( DCS) Basic computer fluency (internet browsers, e-mail, word processing)Asset:Associate or Bachelor degree in technical field Bioworks certificate Completed coursework in biotechnical field Experience in clean room or GMP/regulated manufacturing environment 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 #PRO007356. 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. |
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, United States |
PA |
11/19/2009
|
| Process Engineer |
| Education:BS in chemical/biochemical engineering, pharmaceutical science or chemistry/biology. MS in chemical/biochemical engineering, pharmaceutical science or chemistry/biologyRequired:3 years manufacturing experience in the areas of pharmaceutical process start up and technical transfer or have demonstrated experience in these areas.Must be able to multi-task and work within tight deadlines. This position requires flexibility and the ability to work independently, as well as excellent organizational skills. Strong professional and interpersonal communication skills are also required. Travel will be a requirement of this position at approximately 30% (US, Puerto Rico, and China). Preferred:Experience with packaging operations is desired. The individual should also possess strong business acumen and interpersonal skills.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 # CHE002152. 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 |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Research Fellow |
| Education:Ph.D. degree in biochemistry, pharmaceutical sciences or a related field Required:A broad understanding of the pharmacokinetics and disposition of therapeutic proteins. 3 or more years of industrial or academic experience in DMPK support of Biologics discovery/development programs. Excellent written and verbal communication skills. Preferred:Three or more years of industrial or academic experience in pharmacokinetic/pharmacodynamic (PK/PD) modeling. 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 #PHA000871. 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
|
| Staff Engineer/Scientist |
| Required:BS / MS in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry with at least 2 (for BS) / 0 (for MS) years relevant experience. Has technical expertise in mammalian and/or yeast based systems. Has demonstrated ability for independent project work. 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 is a plus. Working understanding of analytical methods to characterize biologics and /or US/EU regulatory requirements and / or working knowledge of cGMPs is a plus. 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 #SCI003878. 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
|
| Documentation Center Assistant |
| Educational requirements:High School diploma Required skills and experience:Excellent customer service, including phone and in-person communication skills. Advanced computer skills. Familiarity with databases. Strict attention to detail. Ability to follow directions exactly. Ability to work "on-call" as needed. Preferred skills and experience: Prior documentation experience (electronic and hard copy). Experience in a GMP environment. Pharmaceutical industry 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 # ADM004036. 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. |
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
|
| 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 |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Process Engineer |
| Education:B.S. in Chemical Engineering or Biological Sciences plus a minimum of 5 years relevant experience. Preferr M.S./Ph.D. in Chemical Engineering or Biological Sciences with a minimum of 3 years related experience Required:Experience with CIP/SIP/process design Demonstrated leadership and teamwork skills, excellent analytical abilities, established written and verbal communication skills. Experience leading a team 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 # CHE002132. 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 Merck as a result of the referral or through other means. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| US Clinical Operations Training Manager |
| Minimum:
? Demonstrated competency as a Novartis Clinical Research Associate.
? Thorough knowledge of Good Clinical Practices (GCPs), FDA Regulations and clinical trial monitoring practices.
? Excellent presentation and interpersonal skills.
? Excellent organization skills with the ability to prioritize and work effectively in a constantly changing environment.
? Strong written and verbal communication skills.
? Demonstrated ability to coach colleagues at various skill, knowledge and experience levels.
? Knowledge in computer technology and ability to support company use of electronic data systems including Electronic Data Capture.
? Ability to interact with a wide range of people and build strong, positive relationships with the CRA Group Head, DFM, Regional Associate Directors, Field Monitors and other training and development staff.
Preferred:
? Minimum five (5) years experience as a Novartis CRA with a degree in a scientific or health care discipline.
? Previous training experience.
? Working knowledge of Microsoft Office (e.g., Word and PowerPoint) and Lotus Notes. |
| 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, HVAC |
| Education/Experience:
High School Diploma and 2 years of related experience; or Associate?s Degree or technical equivalent and no related experience. |
| 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 |
NC |
11/20/2009
|
| Tech Advisor I/Veterinary |
| Bachelor?s Degree in Scientific Field preferred
? Veterinary clinic experience preferred
? Previous scientific or medical background
? Knowledge of PC package tools including word processing (Word) and spreadsheets (Excel)
? Ability to effectively communicate verbally and in writing
? Ability to define problems, collect data, establish facts and draw valid conclusions
? Ability to interpret a variety of technical and scientific data
? Effective interpersonal skills
? Ability to work independently as well as a team member |
| 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.Regulatory CMC Liaison Manager |
| Education and/or Professional Experience:
Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent.
Desirable:
Advanced degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent.
Languages:
Fluent English required (oral & written). Good skills in site (local) language desired (oral).
Experience/Professional Requirements:
6-8 years in regulatory preferred, and/or experience in drug/biologic pharmaceuticals
Working knowledge/experience in regulatory submission and approval processes for New Chemical Entities (NCE) and product life cycle management and proven practical knowledge of and ability to deal with complex CMC regulatory issues and requirements.
Proven track record of successfully working in interdisciplinary teams, and of planning, coordinating and leading activities simultaneously on multiple projects.
Regularly demonstrated active contributions to line functions or project teams, as well as ability to contribute to matrix teams with the necessary strategic thinking.
Demonstrated ability for strategic thinking, maintaining awareness of business impact.
Demonstrated ability for risk assessment and mitigation.
Computer literacy (e.g. MS-project, Power Point, document management systems) available and shown ability to quickly learn new software and tracking tools and associated processes.
Strong interpersonal, communication, negotiation and problem solving skills. |
| 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 |
CA |
11/20/2009
|
| Sr Technical Project Leader - Vacaville, CA |
| Advanced degree in scientific or relevant discipline or equivalent
Desirable: Ph.D. in scientific or relevant discipline or equivalent
Additional requirements:
Excellent English required (oral & written). Good skills in site (local) language desired (oral).
?Demonstrated 5 ? 10 years of successful performance in the role of leading interdisciplinary teams of scientists working on technical projects within TECHNICAL Line Functions or equivalent experience in line function management or from external company.
?Proven track record as actively contributing Technical Project Team Representative or Project Team Member in IPTs / FIPs for a number of projects within the Novartis group or equivalent experience.
?Demonstrated ability to successfully manage budget(s), resources and associated development plans of assigned projects with adequate proactive planning and communication to involved functions or equivalent experience from line function management (e.g. section budget).
?Proven track record in coaching associates within technical line functions or adequate experience from line function management or external company.
?Significant further professional development such as scientific expertise and understanding in the required areas, advanced and continuous education in project management methodologies and basic commercial principles. |
| 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 |
MA |
11/20/2009
|
| Sr Scientist, Clinical PK/PD |
| Minimum Requirements:
Ph.D. level scientist with biological background with at least 0-2 years experience in drug development or a relevant environment (e.g. Clinical Pharmacology, Drug Metabolism and Pharmacokinetics).
In depth knowledge of PK and PK/PD evaluation techniques required.
Experience of working in a team environment a plus.
Knowledge of regulatory requirements and experience in dealing with regulatory authorities either through written summaries or oral presentations is desired, but not essential.
The individual must be very effective at technical and scientific problem solving in a project driven, multi-disciplinary international environment, able to focus and work on several projects simultaneously and must posses excellent interpersonal, leadership and teamwork skills with very good organizational skills (e.g. planning and time management).
Must be fluent in written and spoken English. |
| 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 Med Scient Expert |
| MD or PhD with unique knowledge for successful clinical
program development and execution, with 3-5 years of
clinical research experience required.
- Fluent English (oral and written)
- Advanced medical/scientific writing and communication
skills
? Proven ability to interpret, discuss and represent
efficacy
and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross
functional team setting, including a matrix environment.
? Demonstrated ability to establish strong scientific
partnership with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area
required; Respiratory expertise preferred |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Sr Director Regulatory Affairs |
| Advanced education degree in life-sciences, engineering or public health or law.
1. Greater than 10 years work related profession experience.
2. 7 years experience in drug/diagnostic regulatory affairs.
3. Knowledge of drug development and regulation affairs requirements
4. Familiar with regulatory issues and challenges associated with Drug/Diagnostic co-development and companion diagnostic.
5. Have a track record in successful data submission for FDA and EMEA approval
6. Sound knowledge of international customs and business practice
7. Profound understanding of molecular technologies and the impact on outcomes and diagnostic results
8. Leadership capabilities working across cultures, expertise and backgrounds
9. Excellent negotiation skills with regulatory staff on various levels of hierarchy
10. Outstanding interpersonal and communication skills for bridging scientific and business participants, for negotiating timelines and for effective international collaboration.
11. Outstanding verbal and written communications |
| 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 |
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 |
NJ |
11/20/2009
|
| Senior Roles-Global Drug Safety & Pharmacovigilance -R&D |
| Education : MD required
Experience: ? Minimum 10 years experience in health care or pharmaceutical industry
? Minimum 4 years of experience in Drug Safety
? Minimum 4 years management experience |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Roles-Clinical Development & Medical Affairs, R&D |
| ? MD degree
? 10+ years experience in the Pharmaceutical industry in OTC and/or Rx Clinical research with commercial savvy
? Experience with development of overall clinical strategy and development plans
? Proven management experience at a senior level
? Demonstrates leadership behaviours by providing vision and direction
? Proven knowledge of drug development processes
? Be able to effectively liaise and influence internally and externally
? Excellent communication and interpersonal skills
? Fluency in written and spoken English, knowledge of French or other European languages beneficial but not essential |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior R&D roles- Category Leads |
| 10-15 years of Pharmaceutical industry experience and/or Over the Counter experience in NRT
? Extensive working knowledge in development along with experience in one or more R&D functional areas (clinical, regulatory)
? Demonstrated track record of leading a complex (e.g. cross-functional, matrix designed) project team
? Demonstrated use of communication and change management strategies/tactics to influence new ways of thinking and working
? Track record of selecting, coaching and developing talent in the organization
? Successfully working across boundaries and building strong external relationships
? Success in situations requiring rigorous, analytical problem solving and the ability to determine scientific opportunity and commercial targets
? Success in effectively communicating and influencing decisions with senior management
? Understanding of global regulatory requirements and impact of public relations
? Mastery of team leadership necessary to work collaboratively with diverse parts of the business, such as marketing
? Demonstrated understanding of the interdependencies of scientific results and commercial possibilities and the use of this knowledge to make appropriate business decisions
? Awareness of cultural differences in different geographic areas and in potentially different approaches to development by an external partner
Education : Phd, Life Sciences or Medical Degree (MD) preferred |
| 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 Finance roles |
| At least 10 years of broad-based financial experience acquired in companies with rigorous and very efficient financial systems |
| Novartis Oncology |
na |
FL |
11/20/2009
|
| Senior Finance roles |
| Education :CPA, MBA
Languages: Fluent English; additional languages are a plus
Experience: - At least 10 years of broad-based financial experience acquired in companies with rigorous and very efficient financial systems
- Experience in headquarters functions and operational finance experience from working in a region or national affiliate
- Experienced in financial responsibility for large scale units
- Several years of management experience, ideally a team of more than 10 |
| 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 |
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 |
NC |
11/20/2009
|
| Scientist IV, Process Dev-TO |
| Education/Experience:
Minimum BS degree in scientific, engineering or life sciences area. 5-8- years with BS; 3-6 years with MS; 0-3 year with PhD or JD |
| 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 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 |
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 |
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 |
NE |
11/20/2009
|
| Project Engineer |
| Minimum Qualifications: Technical Bachelor?s degree, Electrical or Mechanical Engineering degree preferred; at least 3 years project experience; demonstrated ability to manage complex concurrent tasks to completion with minimal supervision.
Knowledge of a technical specialty and/or a general knowledge of industrial or pharmaceutical practices, with pharmaceutical experience preferred. Knowledge of and demonstrated use of project management tools, negotiation techniques, industry accepted construction techniques, statistics, control charting, and process capabilities beneficial.
If you require accommodation under the American's with Disibilities Act to apply for this position, contact (402) 467-8808 for assistance. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Program Section Leader (PSL MD) |
| Education:
Advanced degree or equivalent education/degree in life science/healthcare is required. MD, PhD degree preferred.
Advanced knowledge in medical/scientific area required.
? ?8 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ?4 years of demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical industry.
? ?4 years people management experience required, this may include management in a matrix environment. Global people management experience desirable.
? Strong management, interpersonal, communication, negotiation and problem solving skills.
? Considerable organization awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams.
? Medical/scientific and operational expertise appropriate to the program. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Program Section Leader (PSL MD) |
| Education (minimum/desirable):
Advanced degree or equivalent education/degree in life science/healthcare is required. MD, PhD degree preferred.
Advanced knowledge in medical/scientific area required.
Languages:
Fluent oral and written English.
Experience/Professional requirement:
? ?8 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ?4 years of demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical industry.
? ?4 years people management experience required, this may include management in a matrix environment. Global people management experience desirable.
? Strong management, interpersonal, communication, negotiation and problem solving skills.
? Considerable organization awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams.
? Medical/scientific and operational expertise appropriate to the program. |
| 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 | |