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Search Jobs by Category
| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Principal Scientist I/II - DMPK |
Minimum Requirements
· Ph.D. in a DMPK-related field plus at least 8 years experience in the pharmaceutical industry and in the DMPK discipline
· Experience in representing the DMPK discipline on cross-functional drug discovery project teams
· Demonstrated ability to influence, mentor and supervise staff working toward project progression and candidate delivery
· Thorough knowledge of the DMPK discipline and a successful track record of the application of DMPK principles to drug discovery
· Proven ability to develop and enhance a DMPK area of specialism
· Familiarity with DMPK-related lead identification and optimization techniques
· Familiarity with and commitment to the pragmatic application of DMPK data to the optimization of lead compounds
Skills and Competencies
· Strong leadership attributes and ability to leverage maximum potential from DMPK staff and to influence cross-functional drug discovery project team members
· Excellent team player and ability to work effectively with a variety of personalities
· Breadth and depth of knowledge of the DMPK discipline as it applies to the discovery and selection of high quality candidate drugs
· Strong scientific, strategic and organizational competency in discipline
· Breadth of knowledge and experience in the drug discovery arena
· Demonstrated ability to critically evaluate drug discovery problems and apply physico-chemical and DMPK tools and principles to achieve solutions
· Ability to martial and apply multi-disciplinary resources to achieve drug discovery goals
· Developed expertise in a specific sub-discipline of DMPK with the ability to communicate and apply this expertise to drug discovery challenges
· A focus on speed and delivery while maintaining quality of results
· Excellent verbal and written communication skills
Preferred Background
· Expertise in the principles of DMPK, in the application of experimental techniques to optimize and characterize the disposition of drugs and in managing senior level staff
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| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Translational Strategist - Infection Research |
| Degree level required and minimum years experience:
· A strong candidate would typically have a Ph.D. or M.D./Ph.D. and 10 or more years of experience, or equivalent experience, of which a minimum of 6 years should be in the pharmaceutical industry or other relevant setting
· Experience in anti-bacterial discovery and development is desirable
Competencies (knowledge and skills):
· Internally and externally recognized expertise in a scientific, technical or organizational area and the capacity to apply literature and theoretical concepts to the advancement of Infection portfolio goals.
· Possess strong problem solving skills and the ability to, on the basis of their own experience and analytical skills, ascertain the value of and initiate the use of new techniques for solving problems within and beyond their immediate project.
· Have a complete understanding of the AstraZeneca drug discovery and development process.
· Understand and work towards the AstraZeneca business objectives.
· Be highly productive: consistently generating high quality results within established time frames, even in areas of limited precedent.
· Possess strong knowledge and understanding of relevant database and scientific support software.
· Be a proactive communicator with excellent verbal and written communication and listening skills. Solicit opinions and feedback from others. Deliver presentations that are well thought out, informative and convincing. Able to present work at internal and external meetings when appropriate.
· Able to direct scientific staff and manage their performance.
· Able to effectively negotiate, persuade and influence others in a matrix environment.
· Capable of proposing and implementing scientific, technical or organizational ideas and initiatives.
· Able to manage multiple tasks efficiently, consistently generating high quality results within established time frames, even in areas of limited precedent.
Behaviors:
· Fosters environment of scientific excellence, innovation, productivity and timeliness, leading by example. Is reliable, has strong work ethic, and shows respect for colleagues
· Demonstrates leadership.
· Mentors and provides development opportunities for matrix or direct reports.
· Demonstrates commitment to team goals and consistently demonstrates influence in team & project meetings, advising project teams with respect to technical solutions and potential new approaches for consideration. Seeks solutions to issues that affect team morale and effectiveness
· Proactively shares expertise and ideas and is viewed as a resource by colleagues. Actively seeks to give advice and encouragement to the scientific community, promoting self as an approachable resource.
· Expands personal skills and knowledge as required to be effective. Demonstrates flexibility, open-mindedness, and adaptability. Projects creditability and professionalism. Is candid and honest in discussions
· Act in accordance with all AstraZeneca policies on personnel, SHE, best laboratory practice, etc.
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| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Director Field Medical Physician (CV) |
| · Graduate of a recognized medical school and recipient of an M.D. degree
· Range of 11 - 33 years of clinical practice
· Board certification in cardiology
· Background in academic medicine, clinical research, and familiarity with biostatistics
· Excellent written and oral communication, interpersonal, and organization skills
· Demonstrated ability to proactively and positively engage teams through multiple communications channels including telephone, e-mail, Internet, and face-to-face
· Ability to travel nationally and internationally
Preferred Background
· Other training such as an M.P.H. or other advanced degree
· Experience with or business acumen around working within the pharmaceutical industry
· Experience with pharmaceutical drug development and medical/scientific affairs
· National recognition as a key opinion leader as demonstrated by a track record of scholarship, independent research funding, publications, and membership in national societies
· Familiarity with DDMAC, PhRMA code, and key regulations in the pharmaceutical industry
· Geographically located close to Wilmington, Delaware headquarters
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| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Principal Scientist; Medicinal Chemist |
| * Ph.D. in Chemistry
* 4-10 years experience post-PhD.
* Demonstrated ability to supervise and mentor other scientists preferably at the Ph.D. level.
* Must have thorough knowledge in synthetic organic and medicinal chemistry coupled with a proven track record in drug discovery.
* Must be familiar with lead identification optimization techniques employing parallel synthesis technology and rational drug design and virtual screening approaches to lead optimization.
* Must be familiar with the pragmatic application of DMPK data to the optimization of lead structures
* Experience in leading multi-disciplinary research groups through drug discovery efforts is preferred.
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Director Clinical Research- Early Development Neuroscience TA |
| Minimum Requirements:- Graduate of a recognized school of medicine with an M.D. degree or equivalent.- Specialty training and board certification or eligibility in Psychiatry or Neurology.- Familiarity with biostatistics.- Excellent written and oral communication, interpersonal, and organizational skills.- Ability to travel nationally and internationally.Preferred Background:- Board certification in Psychiatry or Neurology.- Scientific training such as a Ph.D. degree is desirable.- Three to five years experience in drug development/medical affairs (Director).- Knowledge of CDER regulations regarding evaluation and approval of pharmaceuticals (Director).- An understanding of US pharmaceutical safety reporting and surveillance.
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| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Associate Director DMPK (In Vitro) |
| Minimum Requirements:
· Ph.D. in a DMPK-related field plus at least 8 years experience in the pharmaceutical industry and in the DMPK discipline
· Experience in representing the DMPK discipline on cross-functional drug discovery project teams
· Demonstrated ability to influence, mentor and manage staff working toward project progression and candidate delivery
· Thorough knowledge of the DMPK discipline and a successful track record of the application of DMPK principles to drug discovery
· Proven ability to develop and enhance a DMPK area of specialism
· Familiarity with DMPK-related lead identification and optimization techniques
· Familiarity with and commitment to the pragmatic application of DMPK data to the optimization of lead compounds
Skills and Competencies:
· Strong leadership attributes and ability to leverage maximum potential from DMPK staff and to influence cross-functional drug discovery project team members
· Excellent team player and ability to work effectively with a variety of personalities
· Breadth and depth of knowledge of the DMPK discipline as it applies to the discovery and selection of high quality candidate drugs
· Strong scientific, strategic and organizational competency in discipline
· Breadth of knowledge and experience in the drug discovery arena
· Demonstrated ability to critically evaluate drug discovery problems and apply physico-chemical and DMPK tools and principles to achieve solutions
· Ability to martial and apply multi-disciplinary resources to achieve drug discovery goals
· Developed expertise in a specific sub-discipline of DMPK with the ability to communicate and apply this expertise to drug discovery challenges
· A focus on speed and delivery while maintaining quality of results
· Excellent verbal and written communication skills
Preferred Background:
· Expertise in the principles of DMPK, in the application of experimental techniques to optimize and characterize the disposition of drugs and in managing senior level staff
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Scientist - Neuroscience Biology |
| ·PhD plus minimum 2 years of post-doctoral research experience, demonstrated ability to implement independent research as evidenced by a strong publication record related to the desired core discipline.
Preferred Background:
·Behavioral Neuroscience or comparable discipline.
|
| AstraZeneca Pharmaceuticals |
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.
|
| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Alliance Administrator |
| Skills and Experience
? Undergraduate degree. BS in life sciences preferred.
? 2-3 years pharmaceutical/biotech strongly preferred.
? Knowledge of the pharmaceutical business, process and activities preferred.
? Knowledge of the disease areas, drug development activities and commercial processes within AZ preferred.
? Strong proficiency in Microsoft Office
? Excellent time management and organizational skills, detail orientation, and ability to multi-task in a high volume environment with shifting priorities.
? Strong interpersonal skills
- Contract management experience preferred.
Knowledge (Preferred)
? Understanding of the terms within a collaboration agreement
? Understanding of the process of establishing collaborative research ventures
? Understanding of AZ?s Discovery organisation
? Appreciation of EU, US funding systems
? Appreciation of other AZ Functions? activities
? Awareness of applicable RA research areas
? Awareness of drug discovery process
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| 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
|
| 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
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Therapeutic Brand Leader - Design for Launch ; Primary Care |
| Education:
- Advanced degree in science-related field, or other appropriate knowledge/experience (PharmD, PhD, MD)
Experience:
- >3 years managing programs in a team environment
- Strong knowledge of clinical development/operations
- Knowledge of development process and/or commercial strategies
- Ability to manage a diverse group of responsibilities
- Ability to work effectively in a cross-functional team environment
Skills and Competencies:
- Leadership abilities
- Expert technical depth in disease area
- Strategic influencing skills
- Highly developed written and verbal communication skills
- Well-developed initiative ability
- Excellent project management skills.
- Strong organization and time management skills.
- Strong analytical and problem solving skills.
- Knowledge of US business and brand operating models
- Scientific acumen
Preferred
- Minimum 5 years experience in a strategy-setting role within Medical Affairs
- Global experience within the pharmaceutical industry
- Working knowledge of FDA requirements
- Excellent computer skills (Excel, Word, Power Point, etc.)
- Knowledge of information/technology systems
- People management experience
- Negotiation skills
- Knowledge of MA organization
|
| 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
|
| 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
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| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Pricing & Market Access Director |
| ·Graduate/College degree in biomedical science, business or economics
·Knowledge of the needs and expectations of regional payers, insurers and commercial customers in our strategic markets
·Good knowledge of the clinical and value demonstration approaches used by R&D in providing support for price and access
·Experience of leading cross- functional teams to deliver and communicate innovative customer solutions based on detailed customer insight
·A track record of delivery in the payer area, either in terms of strategy development or in influencing payer decision makingA proven track record of being able to integrate their own thinking and activities into the work of other teams
·Experience of developing concise and audience-focused communications, both written and for presentation
·Able to develop models for quantification of scenarios and risk eg financial models, economic/clinical models
Preferred Background:
·Postgraduate qualification in biomedical science, business administration, finance or economics
·Knowledge of the approaches used by R&D in providing support for price and access
·Knowledge of how different factors drive payer decision making at country level
·Knowledge of what evidence is most influential in an HTA submission or formulary pack
·Experience working with clinicians, pharmacists and payers on evidence based customer solutions eg through working with local payers in Europe or commercial customers in the US
·Experience in a marketing company in a commercial strategy function eg managed markets brand director, business development director, head of pricing/access
·Experience constructing payer value stories and incorporating these into TPCs and clinical development programs
·Able to develop simple customer-focused models and tools aimed at regional payers or commercial customers
·Knowledge of pricing methods
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| 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 |
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
|
| Post-Graduate Intern |
| The minimum education, training and experience requirements for the role are:
-A Masters degree and/or a Ph.D. candidate in pharmaceutical sciences or chemical engineering (or related disciplines).
-Completed coursework with the necessary credits for a Masters or Ph.D. degree preferably with electives that would provide a sound theoretical background in the fields of statics, mathematical modelling, material properties etc.
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Patient Safety Principal Scientist Compliance and Support |
| Minimum Requirements ?Education and Experience:
?Qualified to degree level in biosciences or an equivalent healthcare or pharmaceutical industry background with proven competence in Patient Safety/Clinical Development
?At least 5 years Patient Safety and/or Clinical Development experience
?High level of technical competence, with an ability to balance this with industry standards to achieve business goals
?Proven leadership skills, able to resolve conflict
?Able to work with a high degree of autonomy
?Able to work effectively as a member of a cross-functional or global team
?Comprehensive understanding of Patient Safety regulatory obligations
?Able to represent AstraZeneca externally where required
?Able to acquire and assimilate knowledge in different disciplines, disease and therapeutic areas
?Demonstrable professional excellence ? adds value by applying expertise proactively
?Proven good communication skills with ability to work across cultures
?Able to influence whilst maintaining independent and objective views
?Maintains high ethical standards, including a commitment to AstraZeneca values and behaviors
?Good attention to detail
?Good time management
?Fluent in English
?Computer literate
Organizational Behaviors:
?Passion for Customers
?Drives Performance
?Works Collaboratively
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| 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
|
| Senior Safety Medical Director - Cardiac |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in cardiology/cardiovascular disease
· MD background with strong expertise in cardiology, ideally drug-induced cardiac injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Hepatic |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in hepatology
· MD background with strong expertise in hepatology, ideally drug-induced liver injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record.
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Renal |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in nephrology
· MD background with strong expertise in nephrology, ideally drug-induced kidney injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record.
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Scientist Bio Science |
| Minimum Requirements
?PhD plus minimum 2 years of post-doctoral research experience, demonstrated ability to implement independent research as evidenced by a strong publication record related to the desired core discipline.
Preferred Background
?Behavioral Neuroscience or comparable discipline.
Reporting Relationship
?Direct Reports ? none initially
?Indirect Reports - supervise a team of up to two colleagues
Leadership Capabilities
Passion for Customers: Understands one?s customers and uses that insight to provide value
Thinks Strategically: Quickly identifies and acts on opportunities, combining forethought with action. This is based on an understanding of the external environment and its impact on AZ.
Acts Decisively: Makes and acts on decisions quickly and effectively and fosters the same in others. This is based on an underlying courage to enable risk taking for the business.
Drives Performance: Holds self and others accountable for the achievement of performance expectations. Creates an environment that enables others to perform at their best.
Works Collaboratively: Actively creates and promotes cross boundary collaboration with the aim of archive better business results. Boundaries can exist between individuals, geographies, cultures, teams, functions or organisations.
Develops People and Organisation: Demonstrates and genuine commitment to the time and effort needed to develop oneself and others.
|
| AstraZeneca Pharmaceuticals |
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 |
Boston |
MA |
11/19/2009
|
| Senior Associate Scientist ? Compound Management |
| Minimum years experience:
?Typically 3 or more years experience in a Biotech / Pharmaceutical setting post Bachelor's Degree or equivalent
Competencies (knowledge and skills):
?Well-developed understanding of theoretical aspects of discipline and a high level of ability in experimental techniques.
?Regularly demonstrates capacity to apply literature and theoretical concepts to the advancement of project goals.
?Strong knowledge and understanding of relevant database and analytical software.
?Independent planning, execution and interpretation of experiments that contribute significantly to project goals.
?Able to develop logical positions and convince others.
?Highly productive: consistently generates high quality results within established time frames.
?Strong problem solving skills and the ability to, on the basis of their own experience and analytical skills, initiate the use of new techniques and to ascertain their value in solving problems relating to their immediate project.
?Collects, analyzes, and summarizes data for reports and patents, and presents data at project and/or team meetings.
?Delivers presentations that are well thought out, informative and convincing. Able to present work at internal meetings and external meetings when appropriate.
?Communicates effectively with colleagues at all levels, showing well-developed verbal and written communication skills, coupled with an ability to listen, resulting in clear and succinct messages and accurate interpretation of feedback.
?Communicates relevant information from meetings or literature to colleagues.
?Identifies and rapidly informs supervisor and colleagues of issues critical to attainment of project goals and is realistic in ability to overcome problems.
?The ability to manage multiple tasks efficiently.
Behaviors:
?Is reliable, has strong work ethic, and respect for colleagues.
?Commitment to team goals.
?Willingly shares expertise and ideas and is viewed as a resource by colleagues.
?Is candid and honest in discussions.
?Demonstrates flexibility, open-mindedness, and adaptability.
?Act in accordance with all AstraZeneca policies on personnel, SHE, best laboratory practice, etc.
?Expands personal skills and knowledge as required to be effective.
?Projects creditability and professionalism
?Fosters environment of scientific excellence, innovation, productivity and timeliness by example.
Leadership Capabilities:
Passion for Customers: Understands one?s customers and uses that insight to provide value
Thinks Strategically: Quickly identifies and acts on opportunities, combining forethought with action. This is based on an understanding of the external environment and its impact on AZ.
Acts Decisively: Makes and acts on decisions quickly and effectively and fosters the same in others. This is based on an underlying courage to enable risk taking for the business.
Drives Performance: Holds self and others accountable for the achievement of performance expectations. Creates an environment that enables others to perform at their best.
Works Collaboratively: Actively creates and promotes cross boundary collaboration with the aim of archive better business results. Boundaries can exist between individuals, geographies, cultures, teams, functions or organisations.
Develops People and Organisation: Demonstrates and genuine commitment to the time and effort needed to develop oneself and others.
|
| Johnson & Johnson Family of Companies |
Miami |
FL |
11/19/2009
|
| Medical Director Complaint Handling & Safety Surveillance |
| M.D. degree is required for this role. Knowledge and experience within cardiology/radiology and/or drug safety or related activities is required. Five years experience in medical device/pharma vigilance activities is preferred. Basic knowledge of the medical device marketplace associated with successful experience in one or more of the following: clinical, regulatory, quality, customer service or technical applications is required. Ability to travel as needed or requested is required. The ability to use computers and computer based software is required. Current or previous leadership and management experience is preferred. |
| Johnson & Johnson Family of Companies |
|
MO |
11/19/2009
|
| Kansas City, MO: Professional Sales Specialist - LifeScan, Inc. |
| This position requires a 4 year degree, as well as, a minimum of 2 years of outside sales experience preferred. 3-5 years of sales experience in a healthcare professional sales environment or experience in professional diabetes care or related healthcare fields strongly preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. This position may require overnight and/or weekend travel. Excellent written and oral communication skills are essential. Preference will be given to candidates living within 30 miles of the territory, with documented history of proven sales success in outside sales, pharmaceutical, or medical products industry. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| 2009 Fall R&D Co-op |
| Candidate must be enrolled in an accredited college/institution and be in good academic standing Student must be pursing a BS or Graduate Degree in Mechanical Engineering, Materials Science and Engineering, Bioengineering, Electrical or related field. Must be available to work full time (40 hours/week) during the 2009 Fall semester. This position will be located in Somerville, NJ. |
| Johnson & Johnson Family of Companies |
Jacksonville |
FL |
11/19/2009
|
| SENIOR RESEARCH OPTOMETRIST |
| A minimum of an OD degree is required. A MS degree or Formal Corneal and Contact Lens residency program is preferred. A minimum of 2 years experience in clinical research of contact lens products is preferred. Very good oral and written communication skills are required. Knowledge, understanding and application of principles, concepts and practices of clinical research are preferred. Strong organizational, communication and analytical skills are preferred. The ability to manage multiple projects simultaneously is required. Experience with studies under IRB (Investigative Review Board) / Ethics Committee / or FDA (Food and Drug administration) review is preferred. Proficiency in Word, Excel, PowerPoint is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Jacksonville |
FL |
11/19/2009
|
| Manager Clinical Affairs |
| A minimum of a Bachelor's degree is required with a minimum of 8+ years of experience in the Clinical Research of medical devices or pharmaceuticals, or 12+ years equivalent work experience in the Clinical Research of medical devices or pharmaceuticals. Pharmaceutical specific experience is preferred. A degree in a science related discipline is preferred. Supervisory responsibilities or experience is an asset. Complete understanding and application of principles, concepts and practices of clinical research procedures will be required. Knowledge and experience with Good Clinical Practice (GCP) is required. Experience working with Regulatory Agencies is required. Opthalmic experience is an asset. Strategic and tactical Clinical and Business knowledge to gain approval and ensure maintenance of legal marketing status of all products will be required. Strong communication, organizational and interpersonal skills are needed. Broad based technical knowledge and skills in diverse areas of business (e.g. R&D, Operations, QA, laboratories, marketing, etc.) are an asset. Ability to effectively negotiate and influence peers, affiliates and Regulatory agencies to ensure that regulatory and business needs are met will be needed. Must have flexibility to provide innovative approaches to gain marketing approvals globally. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
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 |
Somerville |
NJ |
11/19/2009
|
| Senior Engineer |
| A BS degree required. A MS degree preferred. Minimum 5 years of related engineering (related to electro mechanical devices) experience required. Experience in a highly regulated environment is highly preferred. Knowledge of ISO and cGMP regulations is required. Previous experience with leading and conducting process validation activities required. Experience with electro-mechanical manufacturing processes preferred. Competent working knowledge of DX methodologies, statistical techniques required. Good communication and presentation skills required. A certification in Process Excellence (Green Belt or Black Belt) is preferred. Competent PC literacy including CAD applications preferred. Due to technical upgrades, this requisition is replacing requisition # 0903157. Any candidates who have already applied to requisition # 0903157 are already being considered, therefore, you do not need to apply. |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Principal Scientist Veterinary Surgeon - Somerville, NJ |
| A DVM/VMD (from an AVMA (American Veterinary Medical Association) approved and accredited program) or equivalent degree is required. Board Certification is strongly preferred but not required. Surgical residency training and/or industry experience (minimum 3 years in industry without residency) is required. Scientific publications are required. Experience working in a team environment is required. Highly motivated, self-starting, and strong verbal and written communication skills are required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Ann Arbor |
MI |
11/19/2009
|
| Behavioral Scientist |
| A minimum of a Ph.D. degree in psychology, epidemiology, or public health related fields is required. Background or experience in Healthcare, Psychology, Social Science, or Epidemiology is preferred. A minimum of 3 years of professional experience in health related field is preferred. Experience in a consulting function that draws on direct and indirect resources from within the organization is preferred. Biostatistics, including a working knowledge of SPSS, SAS, or JMP is preferred. Statistical analytical skills that include understanding of predictive modeling, psychometric/tests and measurement, and/or healthcare economics are preferred. Understanding of research methodology is preferred. Professional experience that includes some indication of scholarly activity (e.g. conference presentation, peer-reviewed publications, etc.) is preferred. Excellent customer facing skills, passion for excellence and exceeding customer expectations, strong oral and interpersonal communication skills are preferred. Must be an active listener with the ability to identify new business opportunities. Strong business development and organizational skills are preferred. Strong experience in applied behavioral science is preferred. Strong track record of publications and presentations in the health care field is preferred. Pre-sales support experience with senior level clients (Managed Care Directors, Medical Directors) also preferred. This position requires up to 20% domestic travel. |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Staff Process Engineer |
| A minimum of a Bachelor's degree and a minimum of 9 years of engineering related experience OR a Masters degree and a minimum of 7 years of engineering related experience OR a Ph.D. and a minimum of 4 years of engineering related experience is required. Complex understanding of polymer and engineering fundamentals is required. Experience in a highly regulated industry is required. Experience in the medical device or pharmaceutical industry is an asset. A clear mastery of statistical and experimental engineering techniques is required. Proficiency with Microsoft Office, specifically Excel is required. Experience with Microsoft Project is preferred. Experience with balloon catheter process and polymer bonding is preferred. Experience with Six Sigma/Process Excellence Tools, Training, and/or Certification is preferred. Experience managing complex projects is required. Excellent verbal and written communication skills are required. This candidate will have strong analytical/problem solving skills. Ability to work on cross functional teams is required. The ability to develop and lead teams, strong collaborative skills, and the ability to negotiate and influence are required. This position will require that you be based in Menlo Park, CA and travel 10% of the time internationally and domestically. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Director Health Economics and Reimbursement SNS (Selective Nerve Stimulator) |
| A minimum of a Masters degree in biomedical science, health service research, business or economics is required. Post doctoral experience is also desirable. Health services research and clinical epidemiology experience preferred. At least 5 or more years experience in HE&R function in pharma, biotech, device or other relevant health care environment required. At least 2 or more years experience in device reimbursement required. Strong knowledge of the US and EMEA healthcare system. Prior experience interfacing directly with Evidence-based medicine and Research and development teams. Knowledge of the needs and expectations of regional payers, insurers and commercial customers in our strategic markets. Strong knowledge of evidence generation and value proposition strategy development used in R&D new product development process in order to provide support for price and market access. Experience in leading cross- functional teams to deliver and communicate evidence generation strategy and customer requirements. Experience with the methods and research tools used in Outcomes research, including clinical epidemiology, health economics and health series research. Ability to author, co-author, publish, referee and critique manuscripts relevant to product value. Demonstrated ability to provide constructive and innovative input into complex problems. Good judgment in business decision making. Ability to create a strategic plan by integrating short-, mid-, and long-term objectives. Ability to clearly communicate to a variety of audiences, both big picture ideas as well as technical details. A proven track record of being able to integrate their own thinking and activities into the work of other teams. Experience of developing concise and audience-focused communications, both written and for presentation. Project management experience. Ability to lead and support change. Significant accomplishments and leadership demonstrated internally; externally recognized as a credible peer/leader. Excellent communications and presentation skills; Excellent interpersonal skills. Ability to represent J&J in a leadership capacity at a variety of external forums. Customer centricity - ability and appreciation to clearly understand that customer and their unique needs; ability to translate understanding into effective development and delivery of relevant solutions. Must have skills in the following: Collaboration and teaming; Strategic Thinking; Ability to make sound business decisions; Intellectual Curiosity; ability to be results oriented. Up to 20% US-based travel is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Principal Engineer |
| BS degree in relevant discipline and 14 + years of related engineering experience; MS in relevant discipline and 12 + years of related engineering experience; Ph.D. in relevant discipline and 9 + years of related engineering experience. Has significant complex level engineering experience. PE License is desirable. Four plus years experience in the medical device industry is required. Possess a mastery of theoretical and practical fundamentals and experimental engineering techniques. Ability to manage several projects. Excellent verbal communication skills and written skillsIf you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Sr Engineer - R&D |
| BS degree in relevant discipline and at least five years of related engineering experience is required; or MS degree in relevant discipline and at least three years of related engineering experience. Experience in the medical device industry would be a requirement. Must possess the basic understanding of engineering fundamentals. English communication skills, written and oral is required.Experience with executing design control deliverables is also required. Experience with Cardio Vascular Products will be required in this role.If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
NJ |
11/19/2009
|
| Global Medical Affairs Leader (Oncology/Hematology) |
| This position requires a minimum of a MD degree, with Board Certification/Board Eligibility in Oncology or Hematology. A minimum of 5 or more years of clinical research experience is required. Pharmaceutical industry is highly desirable. For this position, experience in the Medical Affairs environment is preferred. Additionally, prior experience and/or knowledge of the prostate cancer area is strongly preferred. Knowledge of oncology products, both J&J and competitors, is required. A demonstrated track record leading highly matrixed, cross-functional work teams comprised of high-level managers and executives is required. A demonstrated track record of success within Medical Affairs and/or clinical R&D required. Global mindset and direct experience in multiple markets, proven ability to partner cross culturally/regionally is preferred as well as an in-depth knowledge of study methodology, study data reviews and analysis. In this position a successful candidate should have excellent knowledge of study execution, benefit risk management and lifecycle management.. Highly innovative with the ability to drive a complex and changing environment and effectively manage and resolve issues within the TA. Proven ability to act as a medical spokesperson for external audiences is required. Also required is strong experience developing and managing strategic relationships with medical experts/opinion leaders. Strong oral, written, and presentation skills are a must. Proven business understanding. A minimum of 20-25% domestic and international 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 |
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 |
|
NJ |
11/19/2009
|
| Director, Scientific Affairs |
| An MD degree is required. One year of Medical Affairs experience is required. Experience or interest in immunology, hematology, oncology, dermatology and gastroenterology is preferred. Apherisis experience is preferred. The qualified candidate must be scientifically and clinically oriented. The qualified candidate will be someone who has a proven track record of the following: service oriented; enjoys learning and teaching; outgoing and at ease in all situations, self-starter; entrepreneurial; team oriented. Excellent oral (including presentation skills) and written communications skills are required. The qualified candidate must be willing and able to travel up to 70% of the time- both domestic and international. 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 |
Miami |
FL |
11/19/2009
|
| Miami, FL: Territory Manager (Electrophysiology) - Biosense Webster, Inc. |
| A minimum of a Bachelor's Degree is required. A minimum of 3 years of medical device sales experience is preferred. 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. The 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. Prior Management Development classes are 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 |
|
NJ |
11/19/2009
|
| R&D Co-Op- Fall 2010 |
| Candidates must be working towards a B.S., M.S., or PhD degree in Chemical Engineering, Materials (Science) Engineering, Biological or Biomedical Engineering, Biology, Chemistry, Pharmaceutical Sciences, or other related concentration. Candidates must possess a 3.0 GPA or higher. Candidates must be authorized to work in the U.S. for any employer. |
| Johnson & Johnson Family of Companies |
Glendora |
CA |
11/19/2009
|
| TEST LAB SUPERVISOR |
| Education and/or Experience: a Bachelors Degree in Electrical/Mechanical Engineering or related field with a minimum of 5 years industry experience and 3 years medical device experience. It is also required to have System Engineering experience in multi-disciplinary products ( Software and Hardware). Knowledge and experience in development processes and in documentation writing is an asset in this role. Lead, design, develop, and implement test equipment and test specifications is required.Strong knowledge of one or more of the following standards such as ASTM, UL, IEC 60601-1, ISO 8536-4 and ISO 10555-1 & -5 is preferred.Knowledge of GMP and other regulatory requirement is also preferred for this position.OTHER SKILLS and ABILITIES:Test Lab Supervisor will be expected to have strong analytical reasoning with excellent communication skills.Test Lab Supervisor will have the knowledge, skill and ability to provide technical support to project teams.If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Medical Device Systems Engineer (Staff Engineer) |
| A minimum of a Bachelor's degree in Mechanical Engineering, Electrical Engineering, or equivalent discipline is required. An advanced degree is an asset. A minimum of 8+ years of overall work experience is an asset, with 5+ years of specific experience in electro-mechanical machine and/or medical device product design an asset. Experience designing electromechanical systems with software interface with practical knowledge of mechanical systems and electronics is an asset. A minimum of 2+ years working knowledge of software/development methodologies as demonstrated by an ability to develop software architecture is an asset. Knowledge of experimentation methods and statistical techniques is an asset. Knowledge of electronics manufacturing and/or mechanical component manufacturing processes is an asset. Working knowledge of FDA requirements for Class II and III medical devices is an asset. Electrical Safety and EMI/EMC standards knowledge or experience is an asset. Strong analytical skills, excellent written and verbal communication skills, strong organizational skills, and effective interface with project teams, physicians and suppliers will be needed in this role. 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
|
| 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 |
Somerville |
NJ |
11/19/2009
|
| Director, Health Economics and Reimbursement (HE&R) - Strategic Market Access North America |
| A minimum of a Masters degree in biomedical science, health service research, or economics is required. Post doctoral experience is also desirable. Health services research (health economics, outcomes research) and clinical epidemiology experience preferred. A minimum of 5 or more years experience in the Medical Device, Pharmaceutical or Health plan industry is required with track record of scientific and business impact success. Knowledge of reimbursement across treatment settings (i.e., hospital inpatient, hospital outpatient, physician's office, long term care, home health, etc.) is required. Previous reimbursement/market access experience working with health plans and payors is required; an understanding of billing and reimbursement procedures from the facility and payor perspective would be preferred. Understanding of complexities associated with the changing health care environment (i.e., fee-for-services, comparative effectiveness, federal/state health care reform risk, outmigration of care) is required. This position requires strong communication and presentation skills. Knowledge of Medicare, Medicaid, Employers and hospital operations is highly desirable. Understanding process and decision-making criteria for evaluating new technologies and for setting reimbursement rates is highly desirable. A minimum of 50% 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 |
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 |
Cincinnati |
OH |
11/19/2009
|
| Clinical Scientist (1 of 2) |
| A minimum of a Bachelors degree in a biological or closely related science is required. A Masters is preferred. At minimum of 7 years of professional experience in relevant fields of health care, academic research, devices or pharmaceutical industry is required. Experience is preferable to include experience related to the conduct of clinical studies but not required. Strong scientific background and/or work experience in medicine, biology, or a closely related field. Ability to work independently. High degree of self-motivation and direction and the ability to make decisions and accept responsibility of outcomes. Strong interpersonal and negotiating skills when dealing with colleagues and outside professional contacts. 15% domestic 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 |
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 |
|
CA |
11/19/2009
|
| Staff Engineer- FEA Analyst |
| EDUCATION and/or EXPERIENCE: MS in Engineering Mechanics (or related engineering discipline) and three or more years of related engineering experience; or Ph.D. in Engineering Mechanics (or related engineering discipline). Experience with ABAQUS IMPLICIT and/or EXPLICIT software in an industrial setting is strongly preferred.. Experience with Statistical Analysis, Metal Plasticity and Metallurgical Principles is preferable. Experience with using LINUX or UNIX operating systems is strongly preferred. Experience with CAD software is also strongly preferred. Experience in the medical device industry would be an asset. Other skills and abilities include: A clear mastery of theoretical and mechanics principals is required for this position and experience with experimental engineering techniques is an asset. English communication skills, written and oral are required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
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 |
Chicago |
IL |
11/19/2009
|
| CLINICAL RN |
| A minimum of a RN is required. A minimum of 3 years of general clinical experience in an acute care facility is required. Relevant clinical practice experience as a vascular access or ICU registered nurse is a plus. This position also requires demonstrated human relation and excellent communication skills. Experience in planning and delivering formal presentations (large and small groups)is desirable. Organization / planning, skills are required as well as structured thinking in clinical procedure settings. Must have the ability to display decisiveness & good judgment in clinical Must have good collaboration skills and be highly organized and self-directed.and be able to foster positive ongoing customer relations. Ability to work flexible hours, during days, nights and or weekends as necessary is required . Approximately 30% travel is required, including some overnight travel. This position is a Casual Part Time position (19.5 hours). Candidate must reside and be willing to work in Chicago , IL. 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
|
| SAP Global Process Subject Matter Expert - Master Data Management |
| A minimum of a Bachelor's degree is required. A Master's degree is preferred. A minimum of 5 years of experience in manufacturing roles within Operations or Supply Chain is required. A minimum of 2 years of experience within a Master Data Management role is highly desirable. A working knowledge of SAP is required. Experience working in an FDA regulated environment with an emphasis on Validation & Compliance of systems and processes is preferred. Experience working remotely with business partners in a global environment is preferred. Process re-engineering experience is preferred. Experience working with multiple franchises and sectors in a highly matrixed environment is preferred. Experience with any of the following is preferred: Process Flow Diagrams, Business user requirements and Documentation. Professional Certification with CPIM, CSCP, Six Sigma Black or Green Belt is preferred. This position will require up to 20% of domestic travel. This position will be based 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 |
Somerville |
NJ |
11/19/2009
|
| Professional Education Director Biosurgery |
| A minimum of a Bachelor's Degree is required, scientific discipline or Masters Degree preferred. 3 years of medical device customer facing experience or relevant clinical experience required. Minimum 3 years of applicable Orthopedic, Cardiothoracic, NeuroSpine, ENT, General surgery, GYN, Urologic, Plastic and Burn surgery business unit experience andor relevant expertise required. Experience in the planning and delivery of medical device professional education programs strongly preferred. Experience managing professional education components during new product launches and global expansion preferred. Experience in project management including managing multiple complex projects, budgets and analytics preferred. 3 or more years supervisory/management or team leader experience preferred. Customer Focus, Accountability, Collaboration & Teamwork, Project/Process Management, Strategic Thinking skills required. Must have strong desire and skill sets to advance within the organization. 30-60% domestic and international travel required. |
| 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 |
Charlotte |
NC |
11/19/2009
|
| Georgia/North Carolina/South Carolina: Regional Product Marketing Manager: Ortho-Clinical Diagnostics, Inc. |
| To be considered for this role, candidates must possess: A minimum of a Bachelors degree is required. A minimum of five years of medical diagnostic industry experience including sales, product management, and/or technical experience is preferred. Excellent communication, presentation and writing skills are required. Demonstration of leadership and organization/planning skills are very desirable. Experience in infectious disease diagnostics is strongly preferred.A valid driver's license issued in one of the 50 States paired with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Newark |
NJ |
11/19/2009
|
| Newark, NJ: Regional Transfusion Medicine Manager: Ortho-Clinical Diagnostics, Inc. |
| To be considered for this position, candidates must possess: A BS/BA degree in scientific, business discipline, or equivalent experience required. MBA a plus. Diagnostic field sales experience with an emphasis on Blood Bank system and technology selling preferred. Advanced knowledge of customer blood banking processes, along with a working knowledge of the appropriate OCD blood banking products (ID-MTS gel and Provue automation) a plus. Clinical experience or related activities a plus. Knowledge of Microsoft Word, Excel, PowerPoint and Outlook required. A valid driver's license and clean driving record required. Ability to travel as necessary or required, which will include overnight and/or weekend travel. Excellent written, and oral communication skills required, with strong presentation skills preferred. Self directed and self motivated, with a proven track record of career success. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Rochester |
NY |
11/19/2009
|
| Program Manager |
| A minimum of a BS or higher degree in Biochemistry, Chemistry, Bioengineering or related field is required. Five years or more years of relevant technical experience with two or more years in a cross functional leadership role. Cross-functional technical or project leadership experience utilizing a phase-gate process to deliver new products into a regulated industry is required. Knowledge of project management tools and processes including facility with Microsoft Project is an asset. Experience with product project portfolio management is an asset. Design for Six Sigma experience is an asset. Experience in medical diagnostics or device industry is an asset. Experience with technical leadership of assay/reagent development is preferred and knowledge of Quality System Regulation, ISO, FDA and other regulatory requirements for medical device or diagnostic products is strongly preferred. Project Management Professional certification and/or MBA degree would be an asset. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
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 |
Minneapolis |
MN |
11/19/2009
|
| Lab Specialist (Minneapolis Area) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. This position will based in Minneapolis, MN Area. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Tupelo |
MS |
11/19/2009
|
| Lab Specialist (Tupelo, MS) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. This position will be based in the Tupelo, MS Area. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| LAB SPECIALIST, MEMPHIS, TN AREA |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Dallas |
TX |
11/19/2009
|
| Lab Specialist (Western Texas) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Boston |
MA |
11/19/2009
|
| Lab Specialist (Boston South/Providence, RI) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position.This position will be based in the Boston South/Providence, RI area. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Taunton |
MA |
11/19/2009
|
| Manager, Clinical Research |
| Minimum of a Bachelors degree in Science or related Health Field is required in this role with a Masters Degree in Science/related Health Field preferred. Also preferred is an, MBA. 10 years industry experience with 7 years experience in the Pharmaceutical or Medical Device industries is required. Strong leadership skills and the ability to develop successful strategies while fully understanding the complex environment of the assigned program. Experience in multiple functional areas strongly preferred (Clinical, Marketing, R&D, Sales)Significant project management experience with cross-functional, cross-company and international project teams. Clinical trial experience is strongly preferred and international trial experience is a plus.Strong ability to communicate clinical information (concepts and results) in oral and written communication to experts (e.g., KOL, FDA reviewers) and to product development team members (e.g., clinicians, marketing personnel, engineers)Understanding of the contribution of scientific and medical affairs goals to company business strategiesExperience drafting or reviewing technical documents (e.g., Clinical protocols/reports, design FMEAs, IOVVs). Appropriate knowledge of GMP, GCP and regulations required.Proven insight into the integration of science, regulatory, and business principles as it pertains to the successful development of multi-center clinical studies.Understanding of reimbursement landscape in the US and OUS is beneficial.Prior experience in strategic roles, along with excellent written and oral communication skills, and experience presenting to senior management also required.Ability to foster a strong collaborative team environmentDemonstrated ability to collaborate and work effectively in a fast-paced matrix environmentDemonstrated negotiation and conflict resolutions skills, including the ability to influence without clear reporting authorityStrong professional diplomacy Strong organizational skills (e.g., able to manage multiple institutions and/or projects). If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Washington |
DC |
11/19/2009
|
| LAB SPECIALIST (WASHINGTON, DC AREA) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position.This position will be based in the Washington, DC area. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Charleston |
WV |
11/19/2009
|
| LAB SPECIALIST (WEST VIRGINIA) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. This position will be based in West Virginia. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Las Vegas |
NV |
11/19/2009
|
| Lab Specialist Northern Arizona (Flagstaff, AZ or Las Vegas, NV locations) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position.This position will be based in the Northern Arizona area (Flagstaff, AZ or Las Vegas, NV locations). If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! . If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Sacramento |
CA |
11/19/2009
|
| Lab Specialist (Northern California) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position.This position will be based in Northern California. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Clinical Research Associate II (in-house) |
| A minimum of 3 years related CRA experience at medical device or pharmaceutical company required. A minimum of a Bachelors degree is required, preferably in a related field. CRA certification is preferred. Must possess excellent written and verbal skills. Must possess working knowledge of medical terminology and clinical research applications. Ability to interact and work with other departmental personnel and work as a contributing team member. Must be detail-oriented with strong organizational skills. Must have strong basic understanding of research methodology and FDA regulations. Must be able to work independently. Must be innovative, creative and flexible and able to effectively identify and resolve problems. Familiar with MS Office, including Word, Access, Excel and Outlook. Ability to use internet to perform basic research. 40-50% travel is required. |
| Johnson & Johnson Family of Companies |
Fort Washington |
PA |
11/19/2009
|
| Associate Director, Clinical Studies |
| A Doctoral degree in psychology, public health, outcomes research, or related scientific discipline is required. A minimum of 4 years of clinical and/or outcomes research experience including claims, clinician-rating, self-report, and/or biometric measures is required. Expertise in behavioral approaches/therapies within wellness and prevention is preferred. Hands-on statistical analysis skills using SPSS and/or SAS, including multivariate modeling is preferred. Excellent written and oral communication skills are required. Experience with publication record including data-based publications, poster and/or podium presentations at scientific conferences is required. Evidence of strong innovation skills preferred. |
| Johnson & Johnson Family of Companies |
Rochester |
NY |
11/19/2009
|
| ENGINEER II |
| A minimum of a Bachelors degree in Engineering or an equivalent scientific discipline is required. A minimum of 2+ years of related engineering experience is required. An Advanced degree in a relevant discipline and 3+ years of related engineering experience is preferred. Basic understanding of engineering fundamentals is required. Experience in a highly regulated industry is required. Experience in the medical device or pharmaceutical industry is an asset. Knowledge of FDA, cGMP is an asset. Knowledge of PLC, vision (camera), SCADA and HMI systems is required. Experience in manufacturing and quality systems or related applications (OTIS, QERTS, SAP) is strongly preferred. Experience with Six Sigma/Process Excellence Tools, Training, and/or Certification is preferred. Proficiency with Microsoft Project is preferred. Excellent verbal and written communication skills are required. Strong analytical/problem solving skills are a must. The ability to work on cross functional teams is required. This position will be based in Rochester, NY in manufacturing operations. |
| Johnson & Johnson Family of Companies |
|
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 |
Spokane |
WA |
11/19/2009
|
| LAB SPECIALIST- Spokane, Washington Area |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is strongly preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 70% travel will be required for this position. This position will based in Spokane, Washington Area. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Irwindale |
CA |
11/19/2009
|
| ENGINEER II |
| BS in Mechanical/Materials Engineering with minimum of 4 years of Medical Device Experience or MS in Mechanical/ Materials Engineering with minimum of 2 years of Medical Device Experience.Demonstrated proficiency with solid modeling tools, such as Solidworks and other engineering analysis tools.Experience with design of catheters, Sheaths, and/or related accessories are required.Must have at least one example of completing product development life cycle on any disposable medical deviceMust have a strong background of creating Engineering Drawings using Autocad.Must have demonstrated innovation through Patents/Publications or any other technical Reports.Experience with Extrusion, Plastic Part Design, Machining and Molding is a plus.Experience with minimally invasive surgical or catheter based devices is a plus If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
San Francisco |
CA |
11/19/2009
|
| Digital Interactive Marketing Manager (Contract) |
| A minimum of 3 years of interactive marketing, sales, or agency experience is required. Specific focus in building rapid, yet comprehensive and polished custom client presentations is required. A strong understanding of basic marketing principles and how to use qualitative and quantitative information to develop successful solutions and pitches is required. Ability to prioritize and manage multiple projects in busy environment is required. Excellent oral and written communication skills are required. Strong presentation building skills is required. High degree of proficiency in Microsoft Office (Excel, Word, PowerPoint) and Photoshop is required. Must be able to thrive in a fast-paced work environment. Must be a strong team player with a can-do, pitch in attitude. Must be capable of working proactively with multiple departments to achieve results. Agency experience is preferred. |
| 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 |
|
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 |
Irving |
TX |
11/19/2009
|
| Senior Polymer Engineer |
| A minimum of a Master's or advanced degree in a scientific, engineering, or related discipline is required, with a PhD preferred. A minimum of 5+ years of experience in polymer chemistry or a related discipline is required. Knowledge of product design in relation to Medical Device Directives, ISO13485 and 21CFR820 regulations and standards is required, with knowledge of QSR, Canadian Medical Device Regulations, and Japanese Medical Device Regulations an asset. Hands-on experimentalist background with experience in polymer characterization and silicone chemistry is an asset. Understanding of material characterization, structure-property, and utilization towards intended application is an asset. Experience in medical device product development is required. Experience in medical device process development and regulatory process is an asset. Knowledge of Design/Process Excellence (Six Sigma, Lean, etc.) is an asset. Knowledge of Biostatistics, FEA, and Solidworks is an asset. A demonstrated ability to work independently and in team-oriented environments, embracing change, risk, and flexibility will be needed. Must be capable of handling multiple projects/tasks at the same time as well as the ability to listen to customers' needs and develop solutions to meet their requirements. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Diamond Bar |
CA |
11/19/2009
|
| Project Manager, Regulatory Affairs (Diamond Bar, CA) |
| A minimum of a Bachelor's degree in Engineering, Physical or Biological science is required. An MS/Advanced degree is preferred. A minimum of 5+ years experience in the medical industry (Medical Device or Pharmaceutical) is required. A minimum of 5+ years experience in Regulatory Affairs or Quality Assurance of Medical Devices is required. Previous experience with global regulations and regulating agencies is required. Experience developing 510K submissions is required. Experience developing PMA submissions for class III medical devices is highly preferred. Prior experience developing IDE submissions is preferred. Experience conducting submission negotiations with the FDA, including pre-submission identification of requirements and strategy and post submission negotiations is required. Previous experience in labeling and promotional material review is a plus. This position will require 10-15% international and domestic travel. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Santa Barbara, CA: Inside Sales Representative: Mentor Corporation |
| To be considered for this role, candidates must meet the following criteria: Bachelor's degree from a four-year college or university, and one to two years related experience preferred. Inside sales experience within the aesthetics or medical device industry strongly preferred. Knowledge of clinical, surgical techniques and procedures, and medical terminology. Skills in demonstrating a professional phone manner. Must work independently and plan extensively to meet goals. Ability to maintain accuracy, consistency and quality in a fast-paced, multitask environment. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Garden City |
NY |
11/19/2009
|
| Long Island, NY: Account Manager - Ortho-Clinical Diagnostic |
| At Johnson & Johnson we are responsible to our employees, the men and women who work with us throughout the world. Everyone must be considered as an individual. We must respect their dignity and recognize their merit. To be considered for this role, candidates must meet the following criteria: A minimum if a Bachelor's degree. A BA/BS in business or health science is preferred. A minimum of 2 years of outside business to business sales experience is preferred. Valid drivers license and clean driving record is required. Ability to travel as necessary or required, which may include overnight and/or weekend travel. Excellent written and oral communication skills is required. Prior capital equipment sales experience is a plus. If you want to explore the many small-company environments behind the big-company inpact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
New York |
NY |
11/19/2009
|
| New York, NY:- Professional Sales Specialist - LifeScan, Inc. |
| This position requires a 4 year degree, as well as, a minimum of 2 years of outside sales experience preferred. 3-5 years of sales experience in a healthcare professional sales environment or experience in professional diabetes care or related healthcare fields strongly preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. This position may require overnight and/or weekend travel. Excellent written and oral communication skills are essential. Preference will be given to candidates living within 30 miles of the territory, with documented history of proven sales success in outside sales, pharmaceutical, or medical products industry. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Atlanta |
GA |
11/19/2009
|
| Atlanta, GA: Account Manager: Ortho-Clinical Diagnostics, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum if a Bachelor's degree is required. A Bachelors degree in business or health science is preferred. A minimum of 3 years of outside business-to-business sales experience is preferred. Valid drivers license and clean driving record is required. Ability to travel as necessary or required, which may include overnight and/or weekend travel. Excellent written and oral communication skills are required. Prior capital equipment sales experience is a plus. If you want to explore the many small-company environments behind the big-company inpact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Director, Medical Writing - Janssen AI, LLC |
| A minimum of a Bachelor's degree in a science or communication discipline with a minimum of 10 years medical writing experience in the clinical or laboratory setting, OR an Advanced Degree with 7 years medical writing experience in a clinical or laboratory setting preferred. Excellent leadership and management experience. Good understanding of experimental methods, research design, and statistical analysis. Ability to analyze medical data and interpret its significance within a pharmaceutical setting. Ability to interpret, analyze, and present statistical data obtained in a clinical trial. Advanced scientific, technical reading, writing and editing skills. Excellent oral communication skills. Proficient computer and word processing skills. Use of templates and experience with document management systems. Up to 5% yearly travel may be required (International as well as Domestic). If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Head of Biometrics (Senior Director) - Janssen AI, LLC |
| A Ph.D. degree in Biostatistics or closely related field is required. A minimum of 15 years of pharmaceutical experience with at least 5 years of management level experience. International experience is strongly desired. Excellent verbal and written communication skills. Must have a working knowledge of filing regulatory documents and complex statistical methods that apply to all phases of clinical trials. Strong attention to detail and accuracy is a must. Ability to effectively present information to senior management, regulatory authorities, public groups, and other departments. Demonstrated ability to integrate planning efforts across departments to ensure organizational effectiveness. Ability to cultivate internal and external relationships based on trust and respect in anticipation of future working relationships. Demonstrated ability to proactively maximize relationships to enable successful collaboration. Demonstrated ability to facilitate a beneficial resolution of conflict. Ability to articulate a clear vision and help others understand their relationship between their roles, the roles of others and the overall goals of the organization; ability to articulate the reason behind organizational changes and demonstrate flexibility, energy and resilience throughout change efforts. Demonstrated ability to work cooperatively within and outside the organization to accomplish the best outcomes; ability to work in diverse teams to optimize decision-making. Demonstrated ability to provide coaching and feedback to foster professional development while also supporting business goals. 10-15% International and Domestic travel is required. |
| Johnson & Johnson Family of Companies |
Philadelphia |
PA |
11/19/2009
|
| State College, PA:- Professional Sales Specialist - LifeScan, Inc. |
| This position requires a 4 year degree, as well as, a minimum of 2 years of outside sales experience preferred. 3-5 years of sales experience in a healthcare professional sales environment or experience in professional diabetes care or related healthcare fields strongly preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. This position may require overnight and/or weekend travel. Excellent written and oral communication skills are essential. Preference will be given to candidates living within 30 miles of the territory, with documented history of proven sales success in outside sales, pharmaceutical, or medical products industry. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
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
|
| Director, Customer Insight and Market Development - Janssen AI, LLC |
| A Minimum of a BA/BS is required with an advanced degree preferred. 8 or more years of progressive marketing experience is required, preferably in the consumer or devices industry. Extensive line marketing experience, senior brand responsibility, product launch experience, and team leadership is also required. The ideal candidate will have demonstrated success in establishing new markets/new paradigms. Line marketing experience demonstrating commitment to innovation through deep customer insights is preferred. Demonstrated track record participating in highly matrixed, cross-functional work teams composed of high-level managers and executives is preferred. Extensive experience accomplishing objectives through people is preferred. Position requires significant domestic and some international travel (approximately 10%). |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Global Marketing Director Bapineuzemab - Janssen AI, LLC |
| A minimum of a BA/BS is required with an advanced degree preferred. 10 or more years of progressive marketing experience is required, preferably in the pharmaceutical or devices industry. Extensive line marketing experience (prefer strong US experience in an infusion/biological setting), senior brand responsibility, product launch experience, and team leadership is also required. Ideally will have demonstrated success in establishing new markets/new paradigms. Minimum of 2 years strategic global marketing leadership experience. Line marketing experience demonstrating commitment to innovation through deep customer insights is key. Demonstrated track record leading highly matrixed, cross-functional work teams composed of high-level managers and executives. Experience with global R&D programs required. Extensive experience accomplishing objectives through people. Position requires significant domestic and some international travel (approximately 50%). |
| Johnson & Johnson Family of Companies |
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 |
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 |
Raynham |
MA |
11/19/2009
|
| Platform Director |
| A minimum of a BS/BA degree is required with an MBA or other advanced degree highly preferred. A minimum of 6 years of total business experience is required, with at least 2 of those years in the following areas: a combination of R&D and marketing experience, brand or strategy marketing, or new product development project management is required. Medical Device experience is highly preferred. Experience in developing and presenting business strategies is required. Must have the ability to influence without authority across multiple levels. This position requires someone to be both strategic and tactical. Experience with financial modeling is preferred. Must possess demonstrated analytical skills. Must have experience with Voice of the Customer (VOC) and/or Job Outcomes Constraints (JOC) techniques and the ability to translate them. Must be able to utilize both written and oral communication skills to produce effective marketing materials. Must have experience making effective presentations to small and large groups at all levels. Must have experience working in cross functional teams, and be able to engage and get buy in from key internal stakeholders and drive teams towards consensus on product needs/opportunities. This position requires approximately 30% travel primarily domestic with some 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 |
Central Islip |
NY |
11/19/2009
|
| Clinical Account Specialist Long Island, NY |
| Bachelor's Degree (or equivalent), RN, PA-C, CNP is required. MBA preferred. 2 years of experience working (i.e., sales, clinical, management, etc.) in an Operating Room and/or Catheter Lab environment is required. Candidates must have a valid driver's license issued in one of the 50 States and a clean driving record. Ability to travel up to 30% is necessary, which may include overnight and/or weekend travel. Candidates must have excellent written and oral communication skills as well as the ability to excel within a results and performance driven environment with a balanced base and variable compensation package. Ability to wear protective lead in the lab is required. Experience in the cardiology/cardiovascular medical device industry, preferably with EP experience is preferred. Candidates with documented leadership awards and achievements are also preferred. Prior management development classes are a plus. Preference will be given to candidates living within 30 miles of the posted geography. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Jacksonville |
FL |
11/19/2009
|
| SENIOR RESEARCH OPTOMETRIST |
| A minimum of a Bachelors Degree in Optometry, Doctoral Degree in Optometry, PhD in Vision Sciences or MD with specialty in Ophthalmology is required. Post-graduate degree or residency in cornea and contact lenses preferred. A minimum of one year working experience in clinical research of contact lens products or vision science is preferred. It is required for the candidate to have patient care experience. General knowledge, understanding and application of principles, concepts and practices of clinical research are preferred. Working efficiently under pressure, ability to manage multiple projects simultaneously is required. Strong organizational, communication and analytical skills is required. Familiarity with Optics and Wavefront aberrations are preferred. MS/PhD in Physiological Optics is preferred. |
| Johnson & Johnson Family of Companies |
|
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 |
Raynham |
MA |
11/19/2009
|
| Supplier Quality Engineer I |
| A minimum of a Bachelor's degree is required, preferably in an Engineering, Life Science, or a related discipline. This position will require a minimum of 0-2+ years experience (including internships, co-ops, or other related experience). A Masters/Advanced degree is an asset. Other experience that is an asset, but not required, will include: Experience in a highly regulated industry is an asset. Experience in the Medical Device industry is preferred. Experience in the Pharmaceutical industry is an asset. FDA and ISO regulations knowledge is an asset. Auditing knowledge is an asset. Strong communication, teamwork, and problem solving skills will be needed. Knowledge in root cause analysis skills are an asset. Experience or knowledge with machining manufacturing processes and injection molding an asset. Six Sigma, Lean, or ASQ Certification and trainings an asset. This position will require up to 20% travel. |
| Johnson & Johnson Family of Companies |
Raritan |
NJ |
11/19/2009
|
| CLINICAL RESEARCH SOLUTIONS DIRECTOR |
| BA/BS degree required; MBA preferred. At least 10 years business experience in the healthcare industry; specific experience in oncology or oncology diagnostics is preferred. Minimum of 8 years of professional sales & marketing experience with significant business to business pharmaceutical sales experience preferred. At least 8 years people management experience required. A successful and consistent track record of delivering business results in a competitive environment required. A proven track record of successful leadership and strong interpersonal and communication skills are required. Demonstrated ability to lead during periods of change, transition and growth. Demonstrated success in developing a world class organization with strong strategic, analytical and organizational skills with ability to "roll up your sleeves". Demonstrated success in leading the commercial input in collaboration with R&D. Must be able to interface with individuals at all levels of the organization. Approximately 50% domestic and international travel required. |
| Johnson & Johnson Family of Companies |
Raynham |
MA |
11/19/2009
|
| Staff Engineer/ Black Belt Process Driver |
| BS- Engineering, is required for this role and a Master's Degree in Engineering would be a plus. A strong technical background is also required.Black Belt certification in Design Excellence mandatory. A Master Black Belt is an asset in this role.2 years as certified Black Belt leading and delivering significant new product development projectsMedical device experience a significant plus. Experience in a regulated industry is required.Ability to align board members, cross-functional directors/managers and engineers to drive organizational change through effective leadership, interpersonal and communication skillsKnowledge of New Product Development, taking a product from concept through commercialization is a requirement.Ability to teach design excellence tools is required and the ability to help others complete Black and Green belt training is an asset.Ability to prioritize and complete multiple projects on time and within assigned resource constraints. 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 |
Raritan |
NJ |
11/19/2009
|
| DIRECTOR OF MEDICAL AFFAIRS |
| Minimum of an MD or MD/Ph.D is required. At least 10 years industry experience with a proven track record in a medical/clinical environment, particularly within medical affairs in pharmaceutical industry and a specialty in Oncology is required. The individual must have have at least 4 years of experience in Oncology. Experience working within FDA requirements and other government and industry standards (HCC, etc) is required. Must have a communication style and reputation which inspires confidence by our thought leader colleagues and external professional groups. A strong record of accomplisment and peer recognition in previous leadership positions. Must possess a sound ability to act as a medical spokesperson for external audiences and strong experience developing and managing strategic relationships with medical experts and opinion leaders. This individual must possess excellent oral and written communication skills, and an effective manager of people. This role requires a deep well of expertise and global success. You must be able to travel 50% domestically and internationally. |
| Johnson & Johnson Family of Companies |
Albuquerque |
NM |
11/19/2009
|
| Spring Semester Co-op, Ethicon Endo Surgery (ABQ) |
| In order to be eligible for a 2010 Fall R&D Co-op position, candidate must be enrolled in an accredited college/institution and be in good academic standing pursuing a Bachelors or Masters degree in Mechanical Engineering, Biomedical Engineering or related field. Only students in their Sophomore year or above will be considered. A minimum GPA of 3.0 is strongly preferred, with demonstrated leadership/participation in campus programs and/or community service activities. Students must be available to work during session indicated and must be authorized to work in the United States and not require sponsorship in the future. To learn more about Ethicon Endo-Surgery, please visit our website at www.ethiconendo.com. |
| Johnson & Johnson Family of Companies |
Skillman |
NJ |
11/19/2009
|
| Associate Scientist, Preclinical Studies (BetaLogics) |
| M.S. or B.S. with a minimum of 2 years relevant experience in scientific discipline is required. Must show basic understanding of laboratory techniques associated with work assignments. Schedule experiments in the lab and perform research in a timely, competent manner. Able to independently solve routine problems and develop solutions. Recommend modifications to methodology and understand the impact of those modifications on the broader research area. Able to review, analyze, and interpret data, especially as requires in-depth evaluation of various factors of increasing and/or changing complexity. Prepare technical reports, summaries, written protocols, and analysis. Interact with employees inside and outside of the immediate working group in a collegial, professional manner, sharing information and expertise. Foster communication and collaborative teamwork. Provide guidance to new or junior personnel. May serve as liaison to wider internal or external scientific community. Knowledge of GLP is an asset. |
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| Memphis, TN: Professional Sales Specialist, Lifescan Inc. |
| A minimum of a 4 year degree is required. Two years of outside sales experience is preferred. 3 years of sales experience in a healthcare professional sales environment or experience in professional diabetes care or related healthcare fields strongly is preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. This position may require overnight and/or weekend travel. Excellent written and oral communication skills are essential. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
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 |
Washington |
DC |
11/19/2009
|
| Clinical Manager (Certified Diabetes Educator) - Washington, DC |
| A minimum of AS degree is required. A minimum of a RN or RD is required. BSN, MSN, or Pharm D is preferred. Certified Diabetes Educator (CDE) with one year of experience is required. Certified insulin pump trainer is preferred. Prior patient care experience is preferred. Knowledge of insulin pump therapy and management of patient blood glucose levels is preferred. Experience coordinating and conducting diabetes education programs to patients, physicians, and health care professionals is preferred. Previous computer experience with MS Office 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 |
| Johnson & Johnson Family of Companies |
Cincinnati |
OH |
11/19/2009
|
| STAFF DESIGN ENGINEER - ELECTRICAL |
| BS degree in electrical engineering, or related field is required. MS degree is preferred. At least 8 years of experience in the planning, design, and commercialization of electrical or electro-mechanical systems, including embedded software is required. The ideal candidate will have a demonstrated track record of driving technically appropriate solutions and the effective use of new technology. DFSS or similar certifications preferred. Medical products or other highly regulated industry is an asset. Technical leadership and project management, particularly with globally outsourced projects is an asset. RF Analog products with experience in design, test and interconnecting/cabling is a requirement for this role. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
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 |
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 |
Cambridge |
MA |
11/19/2009
|
| REGIONAL ACCOUNT MANAGER- SouthEast (FL, PR, GA,AL) |
|
| 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 |
Dallas |
TX |
11/19/2009
|
| Health Systems Manager - Dallas |
|
| 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
|
| Associate Director/Director, Molecular Medicine |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr. Manager, Regulatory CMC |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Scientist I/Scientist II, Molecular Technologies |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr. Manager / Assoc Director, Clinical Supply Operations |
|
| 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
|
| Scientist I, Chemical Engineer |
| - A Ph.D. degree with 1+ years of pharmaceutical industry experience; an MS degree with 3+ years of pharmaceutical industry experience; or a BS degree with 6+ years of pharmaceutical industry experience. Degrees with a life science concentration required, with a preference for concentrations in chemical engineering or chemistry.
- A demonstrated understanding and working knowledge of chemistry and chemical engineering fundamentals; advanced technical knowledge and experience in API process development, process scale-up, troubleshooting, and optimization; applied kinetics, thermodynamics, and transport fundamentals; as well as familiarity with modern laboratory instrumentation (HPLC, GC, FTIR, Raman, FBRM, DSC, TGA, XRPD, etc), automation tools, and laboratory/plant implementation of PAT
- Experience with modeling complex, physicochemical systems; data analysis; statistical design of experiments; QbD concepts, and fluency with common physical property and process modeling tools (Aspen, Dynochem, Matlab, etc.)
- A track record of successful laboratory and pilot-scale development in the areas of reaction engineering, catalysis, crystallization, separation technologies, drying, and micronization
- The ability to successfully interact, lead, and collaborate within an interdisciplinary team environment comprised of organic, physical, and analytical chemists; project team members; and manufacturing personnel
- Experience with the management of external scientific activities and CRO/CMO relationships
- Proven communication (verbal and written) and interpersonal skills
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Research Scientist I/II |
| The ideal candidate for this position will have at least an MS degree with 6 years, or a PhD with 4 years of hands-on experience in using relevant general pharmacology assays, such as Langendorff perfusion, telemetry, plethysmography, gastric emptying and intestinal transit, or renal function test. Demonstrated ability to analyze, interpret, and report physiological function data is a must. Industry experience and experience with assessing drug-induced QT prolongation is preferred. Extensive knowledge of Data Sciences/Ponemah (P3P and DataQuest) or similar software packages is necessary. Ability to write basic programs using SAS software for data analysis and statistics is a plus. Good team work, strong written and oral communication skills are required, including good report writing and presentation skills.
Vertex Pharmaceuticals |
| 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
|
| Group Leader - Pharmacokinetic |
| PhD degree in relevant scientific field (e.g. pharmacokinetics, pharmaceutical sciences, chemistry or a closely related discipline) or equivalent. A strong knowledge of pre-clinical in pharmacokinetic and PKPD and their impact on drug discovery projects is critical. A seven (7) years post-doctoral relevant industry experience or equivalent. Knowledge of chemistry and physico-chemical properties as applied to drug discovery is necessary. Knowledge and experience with the design of experiments to define PK-PD relationships and competency using non-compartmental techniques and pharmacokinetic modeling software (e.g., WinNonlin or equivalent) is required. Experience having written pharmacokinetic sections of IND is a plus. Excellent cross-functional team leadership and participation skills. Ability to build, lead and manage a group of highly motivated scientists is required. Ability to lead, influence and motivate others, both within direct supervisory and matrixed environments. Ability to demonstrate effectiveness and growth in a fast-paced and dynamic environment. Excellent oral and written communication 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, inflammation, autoimmune diseases, cancer, pain and bacterial infection.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Associate Director, Field Training & Development |
| - Bachelor?s degree with a preference for an advanced degree in business
- 4 + years of specialty pharmaceutical/biotechnology sales training experience
- 3 + years of specialty pharmaceutical/biotechnology sales experience
- In addition to the above, experience in pharmaceutical marketing or corporate training would be advantageous
- Experience in adult education principles including competency modeling preferred
- Proven project management, presentation, interpersonal as well as verbal and written communication skills
- Through the exceptional understanding of state of the art selling skills including clinical and contextual skills, the ability to develop programs to transfer this knowledge to field sales teams
- Demonstrated ability to work independently and manage projects that require collaboration across functional areas including Customer Outcomes Operations, Marketing, Market Research, Managed Markets, Medical Affairs, Finance, Information Technology and Corporate Learning & Development
- Team player able to develop rapport and credibility with key stakeholders
- Solid coaching and mentoring skills that are constructive and motivational
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 |
San Diego |
CA |
11/19/2009
|
| Temporary Scientific Associate (Analytical Development) |
| * Requires a BS degree in Chemistry and 5+ years of relevant experience or MS degree in Chemistry and 3+ years of relevant experience.
* Must have analytical chemistry experience in a pharmaceutical or related field.
* Must have experience using HPLC/GR instruments.
* Chemical Manufacturing & Control (CMC) environment experience is highly preferred.
* Highly self-motivated, you must have good communication skills both written and verbal, be able to multitask, be flexible and have the ability to work in a flexible cross-functional team environment.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| 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 |
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
|
| Project Manager, Research Project Planning |
| We are looking for a minimum of a bachelors degree, or equivalent, and 3 years of biomedical R&D project management experience in a biotech or pharmaceutical company.
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. 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
|
| Senior Engineer |
| Minimum of a Bachelor's Degree or equivalent in Computer Science, Information Systems, Engineering, or related technical discipline (required)
8+ years of experience in security engineering
Integration of AD and LDAP directory stores for authentication (AD) and directory attributes for administration roles, event management, and reporting
Windows, linux, unix, networking technologies experience
Lotus Notes experience a plus
Certifications a plus
Must possess good communication and mentoring 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
|
| 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
|
| Senior Scientist, Process Safety |
| - Ph.D. or BS/MS in Chemical Engineering or Chemistry
- 6 + years of relevant work experience in API or fine chemical process development, scale-up, troubleshooting, and optimization
- A strong and sound understanding of synthetic organic chemistry and chemical engineering fundamentals along with common chemical hazards/incompatibilities with a familiarity with modern in-situ process analysis tools (FTIR, n-IR, UV-Vis) being a plus
- Experience with the application of common safety evaluation instrumentation such as TGA, DSC, RC-1, ARC, RSST and the resulting data in the identification and mitigation of chemical process hazards
- Demonstrated experience with modeling complex, physicochemical systems and statistical design of experiments as well as a fluency with common physical property and process modeling tools (Aspen, Dynochem, Matlab, etc.)
- Knowledge of applied kinetics, thermodynamics, and transport fundamentals
- A nature driven by high productivity and producing results
- The ablity to generate and implement original ideas and solutions that contribute materially to the success and development of drug substance candidates
- Excellent communication and interpersonal skills, strong organization and planning skills, a high level of technical aptitude and creativity, and the ability to interact, lead, and collaborate within an interdisciplinary team environment comprised of organic, physical, and analytical chemists; project team members; and manufacturing personnel
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
|
| Associate Director |
| Experienced in Clinical Pharmacology ie has NCE drug development experience with at least 5 NCEs in the past.
Possesses good knowledge of drug Development Programs and a keen awareness of development issues
Able to integrate the activities of distinct functional groups across multiple projects
Can recognize and carry out productive new development initiatives/directions
Is a mid-level experienced mentor who effectively infuses confidence and team commitment: can make clear written and oral presentations.
Exhibits a record of excellent operational and ethical standards, and team-improvement
Demonstrated ability to provide career development to staff
Able to recognize and resolve important organizational problems and/or infusing innovation
Has leadership abilities, can initiate and carry out tasks with little direct supervision.
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
|
| Associate Director, Market Research |
| - A Bachelor's degree in a quantitative discipline such as finance, engineering, mathematics or statistics with a preference for an advanced degree in business, economics, mathematics, or statistics
- 7 years experience in pharmaceutical and/or biotechnology market research, with a majority of this experience being company or client side
- Experience with managed markets market research including working knowledge of key primary and secondary data sources as well as selection of pricing research vendors and pricing research execution
- Ability to multitask as well as be productive, and innovative, in a dynamic, fast paced environment while working both independently and coaching others on aspects of market research projects
- Strong interpersonal skills along with the proven ability to succeed in matrix team environment. Previous team management experience would be a plus
- Outstanding written and verbal communication skills with the established ability to effectively communicate study results to diverse audiences
- Strong computer skills including advanced competency with PowerPoint. Working knowledge of SPSS or SAS preferred
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company?s strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex?s product pipeline is focused on viral diseases, 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
|
| 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 |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Sr. Scientist/Scientist - Preclinical Bio-Imaging, Agensys - Santa Monica, CA |
| ? PhD with a background in radiology, cancer or cell biology that includes analyzing and interpreting imaging data? Minimum of 4-5 years of industrial or academic experience in relevant fields? Research experience in small animal imaging, managing relevant equipment and interpreting radiopharmaceutical experiments is critical? Experience with use of in vivo models to explore PK, PD and efficacy and their relationship with biomarker expression is highly desirable ? A proven publication record is desirable? Ability to take charge and drive projects to completion? Effective interpersonal and technical communication skills with ability to report and communicate study outcomes to project team(s)? Ability to work in a team oriented environment and oversee portions of studies performed by other groups or departments? Understanding of ALAAC accreditation and IACUC protocols is highly desirable. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Senior Scientist/Scientist, Cell Line Development - Agensys, Santa Monica, CA |
| The successful candidate will have a PhD in biotechnology, cell biology, biochemistry or related discipline with minimum 5 years of relevant industry experience. Other required experience includes expertise in a broad range of molecular and cellular techniques surrounding aspects of cell culture, vector development and expression technologies, cell line development, and cell banking. Experience with management of research associates and demonstrated leadership is preferred. Excellent verbal and communication skills, as well as the ability to work in a team environment are essential. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Senior Research Associate, In vivo validation - Agensys - Santa Monica, CA |
| The ideal candidate should have a MS in biological sciences with a minimum of 5 years experience in biological research, preferably in an industry setting. Previous experience in handling research rodents, especially immunodeficient mice, is absolutely required. Experiences in pre-clinical validation of cancer therapeutics using xenograft models, performing microsurgical procedures in rodents, xenograft tumor characterization and mammalian cell culture are highly desired. We are seeking a flexible, enthusiastic individual with good organizational and communication skills and the desire to work in a dynamic team environment. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Scientist/Sr Scientist, Translational Research -- Agensys, Santa Monica, CA |
| Candidate consideration requires a Ph.D. in molecular and cellular biology or similar field with a minimum of 6 years of post-doctoral experience. Industrial experience in Oncology drug discovery and experience managing research associates is highly preferred. Successful candidates will have strong written and oral communication skills, be self-motivated, demonstrate leadership and possess an exemplary record of research, as evidenced by publications and patents. Developmental opportunities include leading projects for therapeutic antibody discovery, building new technology platforms, and team leadership. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Scientist, Target Discovery -- Agensys, Santa Monica, CA |
| The successful candidate will have a PhD in molecular biology, biotechnology, biochemistry or related discipline with minimum 5 years of relevant industry experience. Other required experience includes expertise in a broad range of molecular and cellular techniques surrounding aspects of microarray-based discovery, biomarker identification and target selection for product development. Experience with management of research associates and demonstrated leadership is preferred. Excellent verbal and communication skills, as well as the ability to work in a dynamic team environment are essential. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate/Senior Research Associate: Target validation and Protein Expression |
| The position requires a BS or MS in Biology or a related field with a minimum 2 years of practical experience in a research laboratory. Industry or academic experience and previous work in biochemical, cancer, immunological, cell culture and molecular biology techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate/Senior Research Associate: Target function ? MAb assays - Agensys, Santa Monica, CA |
| The position requires a BS or MS in Biology or a related field with a minimum 3 years of practical experience in a research laboratory in the required activities. Industry experience and previous work in biochemical, immunological, cell culture and cell-based techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Translational Research - Agensys, Santa Monica, CA |
| Candidate consideration requires a BS/MS in molecular and cellular biology or similar field with a minimum of 3 years of relevant laboratory experience. Industrial experience in Oncology drug discovery is preferred. Successful candidates will have strong written and oral communication skills and be self-motivated. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Target Validation and Protein Expression, Agensys - Santa Monica, CA |
| The position requires a BS or MS in Biology or a related field with a minimum 2 years of practical experience in a research laboratory. Industry or academic experience and previous work in biochemical, cancer, immunological, cell culture and molecular biology techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Target Validation and Protein Expression, Agensys - Santa Monica, CA |
| The position requires a BS or MS in Biology or a related field with a minimum 2 years of practical experience in a research laboratory. Industry or academic experience and previous work in biochemical, cancer, immunological, cell culture and molecular biology techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Target Discovery -- Agensys, Santa Monica, CA |
| The ideal candidate will have a M.S. or B.S. in Molecular Biology or related field, with preferably a minimum of three (3) years of relevant experience in industry. Experience in microarray systems, data analysis, RNA isolation, and real-time PCR is required. Excellent verbal and communication skills, as well as the ability to work in a team environment are essential. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Cell Line Development - Agensys, Santa Monica, CA |
| The ideal candidate will have a M.S. or B.S. in Molecular Biology or related field, with preferably a minimum of three (3) years of relevant experience in industry. Experience in antibody expression systems, production cell line generation, and antibody characterization is required. Excellent verbal and communication skills, as well as the ability to work in a team environment are essential. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate Antibody Production, Agensys - Santa Monica, CA |
| ?X Bachelors, or Masters Degree in Cellular Biology, Bioengineering, Microbiology or a related field. ?X Minimum of 2 years post graduate experience. ?X Extensive mammalian tissue culture experience, preferably gained in an antibody production environment. ?X Knowledge of process development for antibody production from hybridomas or recombinant cells; experience with techniques to improve recombinant protein expression by stable mammalian cell lines is advantageous?X Applicants should be well organized, self-motivated, and capable of working independently and in a collaborative environment. ?X Experience in antibody purification techniques is desirable but not essential as full training will be given.?X Excellent verbal and written communication?X Excellent organizational skills. ?X Meticulous note keeping will be essential |
| 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/Senior Director, Molecular Discovery -- Agensys, Santa Monica, CA |
| ?X Advanced degree (Ph.D., or equivalent) with at least 10 years experience in an industry setting, molecular biology, molecular genomics, bioinformatics and related areas. with demonstrated track record of ?X Proven record in design and implementation of activities related to gene discovery and characterization, gene profiling, bioinformatics, ?X Demonstrated record in driving scientific and technical innovations, as evidenced by first or senior authored publications in top-tiered journals?X Demonstrated successful program leadership and multi-project coordination ?X At least 5 years of management experience of multiple groups ?X Proven track record in leading programs to achieve goals and timelines?X Ability to perform successfully in a cross-functional team environment?X Excellent written and verbal communication skills |
| 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 Line Development Research Associate ? TEMP Position --Agensys, Santa Monica, CA |
| The ideal candidate will have a M.S. or B.S. in Cell Biology or related field, with a minimum of three (3) years of relevant experience. Experience in antibody expression systems, production cell line generation, and antibody characterization is preferred. Excellent verbal and communication skills, as well as the ability to work in a team environment are essential. |
| 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
|
| 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
|
| 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. |
Santa Monica |
CA |
11/19/2009
|
| Manufacturing Associate II-- Agensys, Santa Monica, CA |
| BS in biological or other science related field and 3+ years relevant industrial experience in the manufacture or development of FDA regulated Biological Products. Clinical or commercial manufacturing experience preferred. Broad based technical knowledge with manufacturing equipment (i.e. Bioreactors, filtration, mixers, purification etc.). Excellent organizational skills, written and oral communication skills and ability to multi-task. Must possess mechanical aptitude. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Manufacturing Associate (temp to perm), Agensys, Santa Monica, CA |
| Clinical or commercial manufacturing experience preferred. Broad based technical knowledge with manufacturing equipment (i.e. Bioreactors, filtration, mixers, purification etc.). Excellent organizational skills, written and oral communication skills and ability to multi-task. Must possess mechanical aptitude |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Facilities Department Planner/Assistant |
| ? An Associates of Arts degree preferred? A minimum of two years experience working in an FDA regulated environment? A working knowledge of Computerized Maintenance Management Systems? Self-starter with the ability to work with minimum supervision? Excellent verbal and written communication skills? The ability to multitask and exercise good judgment? The ability to work in a fast pace environment and maintain a high level of customer service? Detailed oriented with good follow-up skills? Proficient in computer usage with standard business software |
| 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. |
| 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
|
| Assoc Dir / Dir Clin Research, Rotation |
| Education:M.D or M.D./Ph.D; Ph.D with substantial post-doctoral experience will also be considered Required:Demonstrated record of scientific scholarship and achievement A proven track record in clinical medicine and background in biomedical research is essentialStrong interpersonal skills, as well as the ability to function in a team environment are essentialPreferred:Prior specific experience in clinical research and prior publication is hightly desirableBoard Certification or Eligibility is preferredConsistently 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 # CLI001986. 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
|
| 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. |
Rahway |
NJ |
11/19/2009
|
| Associate Director Clinical Research |
| Required:-An M.D or M.D./Ph.D, plus Board Certification or Eligibility is preferred. Must have experience in industry or academia Desired:-Previous clinical development experience preferably in biologics or in therapeutic areas of arthritis, clinical immunology, anemia or hematology. 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 # CLI002031. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Chemical Engineer |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001968. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Engineer |
| This position requires candidate to be currently enrolled in a BS program in Mechanical, Industrial, Electrical Engineering or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # ENG002103. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Staff Chemical Engineer |
| This position requires candidate to be currently enrolled in a MS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002019. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Senior Chemical Engineer |
| This position requires candidate to be currently enrolled in a PhD program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002024. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Chemical Engineer |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001998. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Chemical Engineer |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001988. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Chemical Engineer |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001978. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Manufacturing Technical Rotation |
| This position requires candidate to be currently enrolled in a MS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002052. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Manufacturing Technical Rotation |
| This position requires candidate to be currently enrolled in a PhD program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002053. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003868. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003878. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
RTP |
Durham |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003888. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003898. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003908. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
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 Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003918. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003928. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Graduate Intern |
| This position requires applicant to be currently working toward a working toward graduate degree in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Statistics or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000318. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Chemical Engineer |
| Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002008. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating day shift (6AM-6PM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001961. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Lab Animal Vet |
| Education Requirement: DVM or VMD Required:At least 2 years post-doctoral training or experience in laboratory animal science is required along with team orientation. Must possess strong leadership and interpersonal skills. Must communicate effectively with all personnel within department and members of the Merck Research Lab Research community. Demonstrates ability to coordinate activities and careers of subordinates. Desired:Diplomate status, ACLAM is preferred or relevant specialty with an AVMA recognized veterinary specialty organization. At least 4 but no more than 8 years experience or MS/PhD in the specialty of laboratory animal care. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world.We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # LAB000108. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm Representatives Please Read Carefully:Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Process Scientist (Adjuvants) |
| The desired candidates will posses a M.S. or PhD in Chemical Engineering or Chemistry (physical and/or analytical) with 1 to 5 years experience (graduate work may count toward this experience). Proven industrial experience with modeling and characterization of aluminum-containing adjuvants in highly desired. To succeed in this role, the candidate will be highly qualified and have a clear understanding of how physical, chemical and engineering properties of processes relate to controlled formation of precipitated particles and to their structure and properties. The candidate should also be familiar with analytical techniques such as X-ray diffraction, FTIR, and/or NMR. Experience with aluminum-containing adjuvant characterization and identification techniques is considered a plus. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #BIO002469. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Specialist |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 3 years of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends, and to complete several months of training on first shift. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001974. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends, and to complete several months of training on first shift. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
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. |
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. |
Elkton |
VA |
11/19/2009
|
| Staff Engineer - Fermentation Process Support |
| Required:Bachelor degree in Engineering or Science field 2 years experience in an engineering or operations position supporting a manufacturing process through one or more of the following roles: process improvements, monitoring process performance, investigating atypicals and implementing corrective actions, creating standard work for operations, and assisting in troubleshooting of the process. Preferred:Experience with technical support of a GMP (good manufacturing practices) manufacturing process BS degree in Chemical Engineering, Biotechnology, Chemistry/Biochemistry Experience in bioprocess manufacturing Experience with fermentation and/or purification processes for production of proteins Supervisory experience Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002156. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Staff Engineer |
| Education:· B.S in Engineering, Biological Sciences, Chemistry or Physics. M.S. in Engineering, Biological Sciences, Chemistry or Physics preferred.Required:· Minimum of 4 years work experience required; with 2 years of work experience specifically in the field of validation. Specific experience in at least one of the following areas is required:· Filter performance qualification using Filter Integrity testers, bubble point, and diffusive flow testing. Experience in validation desired; alternatively, experience in engineering or operations is acceptable with use of sterilizing filters, tangential flow filtration, ultra filtration, and vent filters.· Container/ Closure Integrity testing using microbial ingress and helium leak testing. Experience in validation desired; alternatively, experience in engineering or operations using welders, sealers, and aseptic fluid transfers using sterile bags and manifolds is acceptable.· Experience in a GMP or ISO13485 laboratory performing microbiology, environmental monitoring or engineering development work. Support the GVTE / BSV Lab Coordinator, with performing instrument qualification, metrology, SOP development , creating training material, lab notebook review, performance of internal audits (chemical hygiene, safety, 5S, GMP), and carrying out improvements activities and corrective actions in response to audits.Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ENG002123. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Staff Scientist |
| Education Minimum Requirement: Bachelors Degree in microbiology, biochemistry, biochemical engineering or related field plus three years related experience. Masters Degree D in microbiology, biochemistry, biochemical engineering or related field preferred. Required Experience and Skills - Strong technical background in cell culture, molecular and microbiology, excellent communication skills, demonstrated ability to troubleshoot bioprocesses, and the ability to work in a team environment. The candidate must be experienced in aseptic technique, be able to work efficiently in a high paced environment and collaborate well with others. Desired Experience and Skills - Virology experience and Assay development. 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 #ENG002118. 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. |
West Point |
PA |
11/19/2009
|
| Research Fellow (Particle Sizing) |
| Education:PhD required Required:At least 5 years of post-doctoral or industrial experience. Candidate must demonstrate expertise and hands-on experience in the application of biophysical methodologies in characterization of biomolecules. Expertise should include theoretical and working knowledge of light scattering methodologies such as multi-angle light scattering (MALS), and varied spectroscopic techniques (CD, AUC, etc.). Qualified candidate is required to be highly motivated and possessing excellent verbal communication and writing skills. The candidate is expected to maintain a high degree of scientific rigor under all circumstances and be accessible to provide scientific supervision. The candidate must also demonstrate ability to work effectively both independently and in a multidisciplinary team environment. The individual can be expected to represent the department at cross-functional team meetings in support of data or decisions arising thereof. Preferred:Experience in innovative solutions to biological particle manipulation, aggregation source, molecular size determination and stabilization over a wide size range of biologics (proteins to viruses). GLP/GMP experience. Significant pharmaceutical experience. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # BIO002487. 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
|
| 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. |
Elkton |
VA |
11/19/2009
|
| Staff Engineer - Protein Purification |
| Required:Bachelors degree in Engineering or Science Discipline 2 years experience in a GMP regulated environment with some or all of that time spent in an Engineering role in support of a process that includes protein purification (will consider a Master's degree in Chemical Engineering, BioChemical Engineering or Biomedical Engineering in lieu of experience) Preferred:Experience with a facility start up Experience with validation qualifications for a start up facility Engineering support experience with a vaccine product 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 #CHE002144. 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. |
Rahway |
NJ |
11/19/2009
|
| Co-op Pilot Plant Operations |
| This position requires students to be in their Sophomore, Pre-Junior, or Junior year, pursuing a Bachelors of Science (B.S) in Chemical or Mechanical Engineering. A minimum Grade Point Average (GPA) of 3.0 is preferred. Prior pharmaceutical experience is a plus. This position is based in Rahway, NJ. Candidate must be available for a period of 6 months. 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 # ADM004029. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Release Coordinator |
| EducationA Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. RequiredAt least three (3) years of relevant post-degree work experience in a manufacturing or research environment or a related field. Strong analytical, problem solving, oral and written communication skills, leadership, and attention to detail. Solid understanding of regulatory requirements and GMPs. PreferredAseptic gowning may be required. Tites may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000134. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Release Associate |
| Required:B.S. degree with a technical emphasis in an appropriate scientific or engineering field. At least one year of relevant post-degree work experience in a laboratory, manufacturing, or quality position. Evidence of leadership skills coupled with good oral and written communication skills, i.e. effective presentation of concepts and ideas, as well as interpersonal and conflict resolution skills. Attention to detail, flexibility and an awareness of production and attendant quality control problems. Preferred:Familiarity with manufacturing batch records is a key skill necessary for success in this position; prior batch record experience is a strong plus. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000124. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Sr. Engineer/Scientist - Manufacturing Process Technical Support |
| Minimum Qualifications: Bachelor's degree in Chemical, BioChemical or Bioprocess Engineering with 5 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR Master's degree in Chemical, BioChemical or Bioprocess Engineering with 2 years experience in a GMP Biopharmaceutical manufacturing or research and development environment Preferred Qualifications:Experience providing technical support of a GMP manufacturing process, specifically in protein purification and/or fermentation. Experience writing technical documentation: such as change controls, protocols, operating procedures. Experience with commissioning, qualification, and validation of biopharmaceutical equipment and processes. Demonstrated expertise in bioprocessing unit operations such as fermentation, chromatography, tangential flow filtration Demonstrated ability to lead a group of individuals in task oriented assignments such as technical investigations, root cause analysis, equipment installation Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002082. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Process Engineer/Scientist - Pharmaceutical Manufacturing Process Support |
| Basic Qualifications: Bachelor's degree in Chemical, BioChemical or Bioprocess Engineering with 7 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR Master's degree in Chemical, BioChemical or Bioprocess Engineering with 5 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR PhD in Chemical, BioChemical or Bioprocess Engineering Preferred Qualifications:Experience leading and developing people and teams Experience and expertise in protein purification or fermentation Project management experience Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002084. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Montreal (West Island) |
QC |
11/19/2009
|
| Researcher in Process Chemistry (Ph.D.), temporary mandate 12 months |
| Education and experience: We are looking for a chemist with an Ph. D. degree in synthetic organic chemistry with a demonstrated skill set (publications, presentations) and who is a creative analytical thinker and has a keen interest to apply his/her talents to the discovery process for new drug molecules. The chosen candidate must be prepared to join a multidisciplinary team and be involved in the entire drug discovery process. Organic synthetic experience in the field of anti-infectious agents will be considered an asset. Ideally the candidate will have completed post doctoral studies and have a minimum of 2 years industrial experience.Language requirements: Good English communication skills (oral and written) are required. Bilingualism, English & French would be an asset. |
| 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. |
Elkton |
VA |
11/19/2009
|
| Sr. Engineer - Protein Purification |
| Required:Bachelors degree in Engineering or Science Discipline 5 years experience in a GMP regulated environment with some or all of that time spent in an Engineering role in support of a process that includes protein purification Preferred:Experience with a facility start up Experience with validation qualifications for a start up facility Engineering support experience with a vaccine product 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 #CHE002143. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Project Scientist |
| Education:BS in Biological Sciences Required. MS in Biological Sciences Preferred Required experience: 3 years post-bachelors degree experience in supply for therapeutic proteins/vaccines/biologics (may be combination of post-graduate education and/or work-related experience.) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #PRO007555. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Staff Biochemist |
| Education:BS in Biological Sciences Required. Required experience: 1 to 3 years post-bachelors degree experience in analysis and supply of biologics (may be combination of post-graduate education and/or work-related experience.) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #PRO007589. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point, 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. |
Montreal (West Island) |
QC |
11/19/2009
|
| Researcher in Chemistry (BS.c/MS.c level), Temporary position 12 months |
| Education and experience: We are looking for a chemist with an B.Sc /M. Sc. degree in synthetic organic chemistry with a demonstrated skill set (publications, presentations) and who is a creative analytical thinker and has a keen interest to apply his/her talents to discover new drug molecules. The chosen candidate must be prepared to join a multidisciplinary team and be involved in the entire drug discovery process. Personal research efforts are also encouraged and applicants should demonstrate interest to contribute to their field. Organic synthetic experience in the field of anti-infectious agents will be considered an asset. Language requirements: Good English communication skills (oral and written) are required. Bilingualism, English & French would be an asset. |
| 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
|
| Lead, Learning & Behavior Realization |
| Educational Requirements: Minimum of five years in a highly regulated industry (preferably pharmaceutical). BS/BA degree in education, science or engineering. Required experience and skills:Minimum of four years experience in instructional design/technology, organizational development, or performance consulting. Excellent communication skills Ability to facilitate cross-functional teams. Ability to collaborate with others. Self-motivated and adaptable Ability to plan and organize work. Ability to learn, understand and communicate business needs and solutions. Ability to solve problems creatively. Computer Skills Ability to drive results. Ability to think strategically. Ability to influence stakeholders. Ability to leverage diversity. 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 #EMP000210 . 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. |
West Point |
PA |
11/19/2009
|
| Quality Engineer |
| Education:Bachelor's degree required. The desired educational background is a BS in an appropriate Engineering field, Operations Improvement, or Business Administration. Other fields of study will be considered if accompanied by significant relevant experience. Required:Three or more years of related Industrial, Production, or Staff experience, obtained through post-degree work in one or more of the following areas: Project management, operations support, or process improvement Financial analysis, resource allocation, or budget / profit plan management Capital plans and/or projects Regulatory and/or compendial requirements Preferred:Experience in one or more of the following areas: Facilities / space planning Operations research techniques Vendor relations and/or contract negotiation 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 # QUA002013. 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 |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Zebrafish Research Associate (BS/MS) |
| Minimum:
? B.S/B.A or M.S. degree in a biological science with a minimum 5 years laboratory research experience
? Proficiency in the use of current molecular biology techniques and cloning strategies, quantitative PCR, site-directed mutagenesis, construction of reporter systems, assessment of protein levels using antibody reagents, and the design and use of various expression vectors
? Experience using gene knockdown, over-expression or microinjection technologies, including RNA interference, to assay the function of pathway activity in.
? Excellent organizational, communication and computer skills.
Preferred:
? General knowledge of zebrafish husbandry
? 1+ years experience in a zebrafish laboratory
? Experience working with a model organism: embryology, genetics and developmental biology principles, whole mount gene expression analysis, phenotypic analysis.
? Familiar with microscopy and imaging. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Wnt Scientific Associate, Developmental & Molecular Pathways |
| B.S. or M.S. in Biochemistry, Cell Biology or Molecular Biology
Minimum 5 years experience in biochemistry, mammalian cell biology working with various cell lines and/or cell signaling mechanisms
Previous experience with stable cell line production, design and analysis of cell-based assays, transfection and viral transduction technologies and genetic knockdown techniques including RNAi is required.
Proficiency in the use of molecular biology and protein biochemistry technologies, e.g. DNA cloning, Real-time PCR, protein-protein interaction, and enzymatic assays is preferred.
Demonstrated ability to evaluate and implement new techniques and technologies.
Experience mentoring and leading scientific associates.
Must be highly motivated, team-oriented, and have excellent interpersonal and communication skills. |
| Novartis Oncology |
na |
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 |
NJ |
11/20/2009
|
| Systems Consultant- Business |
| Principal Programmer
Responsible for all project level programming aspects (analysis datasets, pooled datasets, listings and tables) for drug project.
Major Activities:
1) Manage the programming activities for a global project following internal project management guidelines including resource planning.
2) Act as Program Programmer for assigned project and take a programming leadership role on the B & SR project team.
3) Maintain efficient interfaces with internal and external customers with advice from SR management.
4) Develop and comply with project/study standards and specifications following internal and regulatory guidelines.
5) Oversee programming style, quality of SR contributions and compliance with timelines.
6) Provide SR input and lead sections of Full Developments and Submission Working Groups.
7) Ensure the documents and specifications are consistent and comply with company standards by providing input into study protocol, CRF and data structures.
8) Program, according to specifications, analysis datasets, pooled datasets, listings summaries, figures and tables for Phase I-IV clinical trials and for SCS and SCE. Ensure quality control and quality audit of deliverables.
9) Maintain records for all assigned projects and archive trial/project analysis and associated documentation.
10) Participate in the selection of CROs, as required, and supervise SR project activities for CROs.
11) Train staff on trial and project level activities and internal processes.
12) Participate in or lead non-clinical project activities. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Systems Consultant - Business |
| Education :BA/BS or equivalent experience in mathematics, statistics computer science, life sciences or related field.
Languages: Fluent English (oral and written)
Experience/Professional requirements: (1) Expert knowledge of/experience with SAS software. (2) Good understanding of global clinical trials practices, procedures, methodologies.(3) Good understanding of regulatory requirements relevant to SR (e.g. GCP, ICH) (4) Experience in providing recommendations for maintenance or development of SR global policies, procedures and clinical data presentation standards. (5) Intermediate knowledge of office tools. (6) At least 8 years experience in a programming role preferably supporting clinical trials/ or in the pharmaceutical industry (5 years for MS Statistics/Computer Science graduates) |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Statistician II - Shanghai China |
| ? At least Master?s Degree in statistics or a closely related field.
? At least 2 year of experience in drug development (maybe acquired at a CRO) or a related area (no prior work experience required for Ph.D.).
? Good communication skills, including ability to communicate in English verbally and in writing.
? Ability to give effective guidance to programmers.
? Knowledge of and experience in using statistical software, in particular SAS
Work Location: Shanghai, China |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Programming Specialist |
| Education: BA/BS or equivalent experience in mathematics, statistics, computer science or life sciences or related field.
Languages: Fluent English (oral and written)
Experience/Professional requirement:: (1) Intermediate knowledge of /experience with SAS software. (2) Working knowledge of database. (3) Good understanding of global clinical trial practices, procedures, methodologies. (4) Good understanding of regulatory requirements relevant to SR (e.g. GCP, ICHP (5) Intermediate knowledge of MS Office tools. (6) At least 4 years experience in a programming role preferably supporting clinical trials/or in the pharmaceutical industry (2 years for MS Statistics/Computer Science graduates). |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Principal Biostatistician |
| Education Minimum/desirable): At least Masters Degree in Statistics (or equivalent degree with 6 years of experience or PhD with 2 years of experience.
Languages: Fluent English (oral or written).
Experience/Professional requirement:
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge preferably in relation to the specfic therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills.
6. Good team player. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Oncology Director Clinical Research Physician |
| MD required. Board certified hematologist/oncologist preferred. Advanced knowledge of oncology required. Must have >5 years of demonstrated leadership and accomplishment in clinical trials and/or medical affairs (planning, executing, reporting clinical trials, leading medical affairs activities) in academia/pharmaceutical industry. People management experience and matrix management experience required. Strong leadership, management, interpersonal, communication, negotiation, and problem-solving skills. Ability to think strategically. Organizational awareness (inter-relationship of departments, business priorities), and experience working on cross functional teams desired. Excellent written and oral communication skills, including presentation skills. Fluent oral and written English. Ability to interact effectively with external customers and internal stakeholders. Ability to travel, US and International. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
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 Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr CTH/CTH (nonMD) |
| ? ? 6 years technical, operational and managerial experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organisation.
? Experience in multiple clinical indications and/or TAs is preferable.
? Previous experience leading in parallel several trials; leading multidisciplinary trial teams in a complex matrix environment (including remote).
? Demonstrated ability to establish effective working relationships with key investigators.
? Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and global clinical development process.
? Advanced knowledge of the assigned TA is preferred, with the demonstrated capability to interpret, discuss and represent trial or program level data.
? Previous experience in interactions with Health Authorities is preferable.
? Experience in Neuropsychiatric disease areas preferred (i.e. Schizophrenia, bipolar disorder, depression) |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Brand Manager Prevacid Innovation |
| ? Proven track record of securing results on key initiatives within a consumer packaged goods or Rx environment.
? Excellent understanding and demonstrated application of brand strategy.
? Ability to lead an organization toward superior business results.
? Outstanding interpersonal skills, with emphasis on ability to influence others in all functions and at all levels in the organization.
? Understanding of the intricacies of new product development within an OTC environment a must.
? New product development experience a must with NDA experience preferred.
? College degree required, MBA preferred, and 6-8 years CPG Brand experience.
? Well-developed oral, written, and analytical skills.
In addition, this candidate will be involved in all aspects of brand strategy across the portfolio. The successful candidate could have a number of different backgrounds including packaged goods marketing, Rx marketing, market research and brand strategy. The candidate will be an excellent motivator, comfortable with both formal and influential leadership skills. The candidate must be comfortable interacting with and influencing senior management. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Software Developer/ Architect |
| ? Advanced degree in Computer Science from reputable program with top performance.
? Experience building commercial quality web-based software solutions at significant scale with the most advanced tools including both Microsoft-centric and Java-centric platforms.
? Demonstrated ability to work well as part of a high performing software engineering team.
? Interest in intersection between the life sciences and computer science.
? Willingness and ability to use variety of tools in very heterogeneous environment to achieve science and business goals.
? Experience building and managing ?big data? systems- Strong communications and interpersonal skills |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| siRNA Formulations Scientist |
| Ms in gene delivery or related field with 0-3 years of relevant experience in the pharmaceutical industry
Bs in gene delivery or related field with 3+ years of relevant experience in the pharmaceutical industry |
| 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-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 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
|
| Scientist, Pharmacokinetics |
| EDUCATION/EXPERIENCE:
Ph.D. with 1-3 years or MS with 5-8 years of experience in one or more areas biopharmaceutics, pharmacokinetics, drug metabolism, bioanalytical chemistry, biostatistics, PK modeling, in vivo-in vitro correlation (IVIVC), and clinical endpoint BE study design/conduct. Inhalation experience a plus. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientist-Biochemical & Organ Toxicology |
| Technical Skill Sets
? Good skills in isolating and cultivating cells from different organs in different species
? Good skills in performing a variety of biochemical techniques (e.g., preparation of cell and tissue extracts, subcellular fractionation, enzyme assays, ELISA, Western blots, ?).
? Good skills in performing a variety of molecular biology techniques (e.g. nucleic acid purification, cloning, PCR)
? Good understanding of SOPs as well as their practical implementation
? Fluency in English
? Working knowledge of relevant IT systems
Experience
? At least 3 years of experience in cellular biology or toxicology in either academic or industrial environment
? Working experience with mammalian cell culture models (primary cultures and cell lines) and related techniques
? Working experience in molecular & biochemical analytical techniques
Personal Skill Sets:
? Interpersonal and teamwork skills
? Good oral communication and writing skills
? Computer skills for experimental organization, assay design, data collection and analysis, and report writing
Education
Bachelor or Master degree in life sciences, preferably biochemistry, pharmacology or biology. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientist or Scientific Associate, Formulations |
| A Ph.D. in Pharmaceutical Sciences, Biochemistry, Chemical Engineering or related life science field with a 0-2 years of post-doctoral experience or an M.S. in relevant field with 2-3 years of Biotechnology/Pharmaceutical industry experience is preferred.
In-depth knowledge of protein structure, chemistry and various degradation and aggregation mechanisms and should be able to apply these principles for designing stable formulations.
Hands-on expertise in liquid and lyophilized formulation development is highly desirable.
Hands-on experience with various biophysical and physio-chemicall characterization techniques, such as CD, FTIR, fluorescence, DSC, light scattering, size-exclusion chromatography, gel electrophoresis etc is highly desired.
Candidate should be detail-oriented and demonstrate problem solving and organization skills.
You must be a strong team player and have the ability to multi-task. |
| 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 I, Mammalian Cell Line Development |
| A B.S. or M.S. degree in biology, cell biology, immunology, or related life science field and 3 plus years of experience in biotechnology or pharmaceutical industry are required.
Recent Ph.D. graduates will also be considered.
The Scientist must be able to work independently to design experiments and perform therapeutic protein expression and production runs to accomplish team goals. Candidate should bring a highly collaborative spirit with an ability to work on multiple projects and maintain well organized records and notebooks.
The successful candidate should also have excellent written and oral communication skills, and be able to thrive in our fast-paced and dynamic organization. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientist - Animal Models Laboratory |
| The preferred candidate will therefore have strong experience in animal experimentation design and execution, drug administration, and small animal surgery. The preferred candidate will have knowledge of mechanisms of drug pharmacology and toxicity and biological approaches to study such mechanisms.
Specific responsibilities include execution of diverse animal experiments. The candidate will help the AM Lab Head plan, interpret and present experimental results. The candidate is expected to work autonomously, requiring minimal guidance on major activities, and to collaborate productively and cooperatively with Laboratory Animal Support (LAS) services. Secondary responsibilities include laboratory maintenance, ordering, oversight of junior technical staff, regular participation to project team meetings as assigned, maintaining orderly and up-to-date laboratory records in accordance with best practices for a GLS-practicing (GLP-like) laboratory.
BA, BS, MS required in life sciences or relevant related field. Medical, surgical, veterinary, or specialized animal experimental training is preferred.
Experience
- In vivo pharmacology.
- Small animal surgery.
- Coordination and cooperation with existing animal study support services and personnel.
- Laboratory Management.
- Molecular & cellular biology skills/techniques.
Technical Ability
- Drug administration to animals, including PO, IV, IP.
- Small animal surgery, such as adoptive cell transfer, vascular dissection, etc.
- Collection of body fluids from living small animals, such as urine and blood.
- Small animal necropsy and tissue collection.
- Molecular and biochemical techniques, such as PCR-based genotyping, qPCR, Western blotting, ELISA, and multiplex immunoassays
- Laboratory maintenance.
- Cost and inventory control at the laboratory level.
- Excellence in data summarization.
Presentation
- Excellent oral and written communication skills. Able to independently summarize role of team, experimental approaches and findings, and potential value.
- Able to present and defend data in lab meetings, as well as during external liasing and project team meetings.
- Able to prepare written reports, for AM, Translational Toxicology, iTox, and external consumption.
Three-five years minimal required years of experience
Rational/Justification: Senior Scientist Technical position essential to support work in the laboratory. Translational Safety Biomarkers and Animal Models (TSBAM) is a new laboratory with a mission to provide innovative, fit-for-purpose animal models for project-driven safety studies. We have hired only the Lab Head of the Animal Models Lab, and lack technical support for delivery of defined objectives. This technical position is prioritized to support the Lab activities aligned with the overall safety strategy, and to move high priority activities forward. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientific Education Manager ? Translational Sciences |
| MD, or PhD with strong research experience in life sciences, clinical sciences, or pharmacology, and at least 3 years of postdoctoral training or professional experience in the biopharmaceutical industry. The candidate must have a working knowledge of early drug development. Experience with clinical trials and/or in initiating scientific education programs or training is a plus. Domestic and international travel will be required. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientific Associate II, Protein Design |
| This role requires a BS or MS in Biology, Biochemistry, Molecular Biology or Immunology and a minimum of 3 years of relevant
working experience. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientific Associate II, Protein Design |
| This role requires a BS or MS in Biology, Biochemistry, Molecular Biology or Immunology and a minimum of 3 years of relevant
working experience. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientific Associate II, Protein Design |
| This role requires a BS or MS in Biology, Biochemistry, Molecular Biology or Immunology and a minimum of 3 years of relevant
working experience. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Research Scientist-Pre-clinical MRI |
| A BS/MS or PhD degree in Bioengineering, or related field.
A minimum of one year experience with small animal Magnetic Resonance Imaging is required. PET experience is a plus. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Research Associate ? Muscle |
| BS/MS degree in biology or equivalent with 3 to 5 years of bench experience in either academic or industrial research setting.
In vivo work: experience in various injection techniques, tissue collection and processing is required. Histology and Immunohistochemistry: sectioning, staining and image analysis/interpretation is a plus.
Biochemistry: protein purification, immunoprecipitation, gel electrophoresis and Western blotting.
Molecular Biology: PCR/RT-PCR, primer design and optimization is a plus.
Cell culture: sterile techniques, cell passaging, cryo-preservation and recovery.
Effective communication skills, attention to detail, ability to work effectively on project teams, self-starter attitude, and intellectual curiosity |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Research Associate - In Vivo Physiology ? Muscle Disease |
| The role requires:
BS/MS degree in physiology, pharmacology, animal science or related fields with 3-5 years experience in a pharmaceutical industry or academic setting
Strong in vivo skills are essential
Experience with models of muscle disease/dysfunction and muscle electrophysiology preferred
Good interpersonal and communication (both oral and written) skills, and ability to work efficiently both independently as well as in a collaborative environment
Meticulous record keeping and attention to details
Ability to organize/prioritize work and meet deadlines in the face of multiple and competing demands
Experience in tissue culture (especially of muscle cell lines), histology, molecular biology and biochemistry methods (e.g., RNA, DNA and protein assays) and genetics (managing genetic models) a plus |
| Novartis Oncology |
na |
HI |
11/20/2009
|
| Regl Scientific Mgr/Dir (Hawaii) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 3 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare/ managed markets environment.
Field-based medical and/or managed care with teaching experience preferred. Thorough knowledge of clinical medicine, managed markets, pharmacoeconomics, disease management, and medical research. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science-oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Operating Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Salary flexible. |
| Novartis Oncology |
na |
UT |
11/20/2009
|
| Regl Account Scientific Asc Dir/Director (AZ, CO, NM, NV and UT) |
| Position will be filled at level commensurate with experience.
MD, PharmD, or PhD with 4 years Post-Doctoral experience required. Field-based medical and/or managed care experience preferred. Thorough knowledge of clinical medicine, managed markets, pharmacoeconomics, disease management, and medical research. Excellent interpersonal communication and presentation skills, (including ability to network), strong personal integrity, teamwork abilities and a customer focus are necessary. Must possess a thorough understanding of the FDA, OIG, HIPAA, and GCP/ICH guidelines relevant to the pharmaceutical industry. Must be able to organize, prioritize, and work effectively in a constantly changing environment. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Ability to interface effectively with a variety of technical platforms for the collection, review, and dissemination of medical information. Demonstrated record of scientific/medical publication. Demonstrated knowledge of GCP practices and standards. Demonstrated technical expertise in at least one disease or therapeutic area. The RASM/D position is associated with approximately 60% travel. Salary flexible. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Regional Associate Director US Clinical Operations, Oncology |
| ? BS degree in a scientific or health care discipline.
? Expert in Oncology with established contacts in the medical community
desired
? Demonstrated skill sets, competency, and proficiency in clinical research
and relevant people management skills.
? Thorough understanding of international aspects of the drug development
process
? Extensive knowledge of GCP/ICH, FDA, local regulations, and trial
monitoring practices
? Matrix management skills in a local and global environment
? Excellent writing, oral and interpersonal communication skills as well as
strong organizational skills
? Proficiency in relevant computer software applications
? Ability to travel a minimum of 50%
? Ability to interact/communicate in matrix organization.
? At least 6 years experience in clinical research.
? At least 2 years supervisory experience is preferred.
? At least 5 years monitoring experience is preferred.
? Experience in project management a Plus
? Strong computer knowledge in Word, PowerPoint, Excel and Lotus Notes
At least 6 years |
| Novartis Oncology |
na |
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 |
IA |
11/20/2009
|
| Professional Services Veterinarian, Swine-Midwest |
| DVM Degree (required)
Good record keeping abilities
Ability to effectively communicate and have effective interpersonal skills.
Knowledge about swine production medicine
Computer skills |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Product Director/Assc Dir Regional Marketing Leader |
| Education: University degree in marketing or related
Fluent English and Spanish preferred
7-10 years operational marketing / product management experience (including Country-level product management, fast moving consumer goods branding or marketing support functions)
Pharmaceutical sales experience (minimum 6 months sales rep rotation)
International experience or worked with international marketing teams as a local product manager
Launch experience with new products or major line extensions
Experience in clinical development or Pharma project management
Experience in pharmaceutical brand/product communications
Exposure to multi-country product launches
Bilingual in English/Spanish is strongly preferred
Therapeutic areas of expertise - Oncology, Transplant, or AIDS is stongly preferred. |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Process Validation Engineer III |
| EDUCATION/EXPERIENCE:
BS and 4 years of related experience in Pharmaceutical or related industry or MS and 2 years of related experience in Pharmaceutical or related industry or PhD and no significant experience |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Principle Med Scien Expert MD |
| ?Advance 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 nephrology/transplantation required. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Principal Scientist (GMP Facility Manager/Engineer) |
| Education
Minimum: BS/MS or equivalent with greater than 8 years of experience.
Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent) with a minimum of 5 years of experience.
Languages: Fluent English (oral and written)
Experience/Professional Requirement:
1. Successfully demonstrated several years (minimum of 3 years) of directly related experience as senior scientist of Ph.D. with post-doctoral/industrial experience (minimum of 1 year) or equivalent.
2. Successfully demonstrated expertise in a specific scientific/technical area.
3. Recognized achievements in the development of new lab/plant procedures.
4. Excellent knowledge of laboratory and/or technical tools.
5. Proficient in utilization of special tools/equipment, lab automation tools and specialized facilities e.g., containment/sterile labs.
6. Thorough understanding of development activities and processes in a specific function.
7. Good knowledge of software and computer tools.
8. Profound literature search skills.
9. Good presentation skills and scientific/technical writing skills.
10. Strong scientific leadership skills.
11. Strong knowledge of relevant SOP, GLP, GMP and Novartis regulations and policies. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Principal MSE |
| MD or PhD with unique knowledge for successful clinical program development and execution, with > 6 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. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Presidential Post Doctoral Fellow |
| Multiple positions exist at all sites of Novartis Institutes for BioMedical Research for individuals with the following minimum requirements: Ph.D. in biological sciences, chemistry, or computer science. Applicants who have commenced postdoctoral training may apply as well, but they should not have been in postdoctoral training for more than 3 years. Candidates must be able to work independently and also participate in team efforts. Excellent oral / written communication and presentation skills and scientific creativity are essential. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Postdoctoral Fellow, DMPK |
| Ph.D. degree with 0-3 years of post-PhD research experience in pharmacokinetics, biopharmaceutics, biomedical engineering, chemical engineering, or other related discipline with specific experience in PK/PD and/or PK modeling is required. The candidate must be able to work independently and have a strong understanding of PK/PD. The candidate should should be able to provide technical assistance on individual projects, spanning across multiple therapeutic areas. Hands-on experience in PK and PK/PD modeling is a must. Good oral and written communication skills are required. Previous experience with some of the PKPD softwares such as: WinNonlin; ADAPT; NONMEM, GastroPlus. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| PhD Scientist: Antibody Therapeutics |
| Molecular Biology lab head Qualifications:
? Ph.D. in molecular biology or life science
? Minimum 3 years of post-doctoral experience in life-science and/or antibody therapeutic research. Industry experience is a plus.
? Self-driven and creative personality
? Excellent written and oral communication skills
? Extensive experience in molecular biology, cell and biochemical assay development and analysis |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| PhD Research Investigator- Oncology Cellular Assay |
|