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Job Title	City	State	Posted on
AstraZeneca Pharmaceuticals	Boston	MA	11/19/2009
Principal Scientist I/II - DMPK
Minimum Requirements · Ph.D. in a DMPK-related field plus at least 8 years experience in the pharmaceutical industry and in the DMPK discipline · Experience in representing the DMPK discipline on cross-functional drug discovery project teams · Demonstrated ability to influence, mentor and supervise staff working toward project progression and candidate delivery · Thorough knowledge of the DMPK discipline and a successful track record of the application of DMPK principles to drug discovery · Proven ability to develop and enhance a DMPK area of specialism · Familiarity with DMPK-related lead identification and optimization techniques · Familiarity with and commitment to the pragmatic application of DMPK data to the optimization of lead compounds Skills and Competencies · Strong leadership attributes and ability to leverage maximum potential from DMPK staff and to influence cross-functional drug discovery project team members · Excellent team player and ability to work effectively with a variety of personalities · Breadth and depth of knowledge of the DMPK discipline as it applies to the discovery and selection of high quality candidate drugs · Strong scientific, strategic and organizational competency in discipline · Breadth of knowledge and experience in the drug discovery arena · Demonstrated ability to critically evaluate drug discovery problems and apply physico-chemical and DMPK tools and principles to achieve solutions · Ability to martial and apply multi-disciplinary resources to achieve drug discovery goals · Developed expertise in a specific sub-discipline of DMPK with the ability to communicate and apply this expertise to drug discovery challenges · A focus on speed and delivery while maintaining quality of results · Excellent verbal and written communication skills Preferred Background · Expertise in the principles of DMPK, in the application of experimental techniques to optimize and characterize the disposition of drugs and in managing senior level staff
AstraZeneca Pharmaceuticals	Boston	MA	11/19/2009
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
Senior Patent Attorney (Multiple Positions)
· BS/MS ? Organic Chemistry and JD ·7+ years of patent experience · Background in organic/medicinal chemistry · Significant experience preparing and prosecuting small molecule patent applications · Excellent interpersonal skills · Strong communication skills Preferred Background · PhD in Organic Chemistry · Global patent experience in the pharmaceutical industry
AstraZeneca Pharmaceuticals	Delaware	DE	11/19/2009
Senior Patent Litigation Attorney
· JDdegree plus 6-8 years employment in patent litigation as a private practice litigation attorney or in-house litigation counsel. · Litigation-team management experience. · Excellent oral and written communications skills, and human relations skills. Preferred: · Patent litigation experience in Hatch-Waxman matters or cases involving pharmaceutical or biotechnology arts. · An educational background in biology, biochemistry, chemistry or similar arts · Registration in the US Patent and Trademark Office.
AstraZeneca Pharmaceuticals	Delaware	DE	11/19/2009
Principal Patent Attorney
· BS/MS ? Organic Chemistry · JD (US); Qualified EPA (Europe) · 10+ years of patent experience or 5+ years of post-qualification experience (Europe) · Background in organic/medicinal chemistry · Highly experienced in US and European Patent Law and Litigation matters · Significant experience preparing and prosecuting small molecule patent applications within or for the pharmaceutical industry · Excellent interpersonal skills · Strong communication skills Preferred Background · PhD in Organic Chemistry · Global patent experience in the pharmaceutical industry
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
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
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
Scientist Bio Science
Minimum Requirements ?PhD plus minimum 2 years of post-doctoral research experience, demonstrated ability to implement independent research as evidenced by a strong publication record related to the desired core discipline. Preferred Background ?Behavioral Neuroscience or comparable discipline. Reporting Relationship ?Direct Reports ? none initially ?Indirect Reports - supervise a team of up to two colleagues Leadership Capabilities Passion for Customers: Understands one?s customers and uses that insight to provide value Thinks Strategically: Quickly identifies and acts on opportunities, combining forethought with action. This is based on an understanding of the external environment and its impact on AZ. Acts Decisively: Makes and acts on decisions quickly and effectively and fosters the same in others. This is based on an underlying courage to enable risk taking for the business. Drives Performance: Holds self and others accountable for the achievement of performance expectations. Creates an environment that enables others to perform at their best. Works Collaboratively: Actively creates and promotes cross boundary collaboration with the aim of archive better business results. Boundaries can exist between individuals, geographies, cultures, teams, functions or organisations. Develops People and Organisation: Demonstrates and genuine commitment to the time and effort needed to develop oneself and others.
AstraZeneca Pharmaceuticals	Delaware	DE	11/19/2009
Intern - Newark Manufacturing
Qualifications: -Major in Supply Chain -3.0 GPA or higher -Leadership experience demonstrated through extracurricular activities and organizational memberships
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	Cincinnati	OH	11/19/2009
Quality Systems and Compliance Specialist
Minimum of a BS or BA in Business, applied Sciences, Quality or an Engineering-related discipline or equivalent work experience is required. CQA certification is strongly preferred. CQE and/or CRE Certification is also preferred. A minimum of 7+ years of total work experience in Regulatory Affairs and/or Quality Assurance in a medical device or pharmaceutical environment is required. Strong auditing skills are required. Experience managing or participating in internal audit programs is also required. Strong Project Management skills, excellent verbal and written communication skills, influencing management skills are required. Knowledge of ISO-GMPs is required. Knowledge of GLP, GCP Quality Systems and international requirements is preferred. Knowledge of design and development, labeling and manufacturing systems is required. Knowledge of continuous improvement principles is preferred. Experience and/or interactions with a Regulatory agency is preferred. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! Johnson & Johnson is committed to diversity and invites all interested candidates to apply for positions of interest. EOE M/F/D/V Please note: In order to be considered eligible for an interview, candidates must apply online through the appropriate web portal.
Johnson & Johnson Family of Companies	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	Somerville	NJ	11/19/2009
Regulatory Affairs Specialist
A minimum of a Bachelor's degree in Biology, Biochemistry, Immunology or a related discipline is required. A PhD degree in Biology, Biochemistry, Immunology or a related discipline is strongly preferred. A minimum of 2+ years experience in Regulatory Affairs required. Experience or exposure to the field of Biologics is required. Medical Device and Pharmaceutical experience is an asset. US Regulatory experience is required. EU and International Regulatory experience is an asset. Previous experience in regulations and submitting files for health authorities in Israel is an asset. Excellent communication skills will be necessary for this role. This position will require 10% travel and will be located in Somerville, NJ.
Johnson & Johnson Family of Companies		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	Somerville	NJ	11/19/2009
Scientist, Biosurgicals R&D
A minimum of a Bachelors degree is required, with a Masters degree or Ph.D. in Biochemistry, Molecular Biology, Cell Biology, Immunology or a related discipline is preferred. A minimum of 1 year of related experience is required. Must have the ability to independently design and execute experimental studies, analyze and interpret study results. In-depth knowledge and development experience in hemostasis and thrombosis, and materials design for blood-contacting applications is required. Must be able to effectively document data in notebooks, in oral presentations and writing reports. Proven track record of research and multi tasking in a Research & Development environment. Familiar with IP evaluations and product development is preferred. Previous experience in technology evaluations: an understanding of general biotechnology principles are preferred. Awareness and understanding of advanced bioanalytical techniques and test method development and validation processes are preferred. If you want to explore the many small company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today.
Johnson & Johnson Family of Companies	Somerville	NJ	11/19/2009
Staff Scientist - Analytical Chemistry
A minimum of a Ph.D. in Polymer Science, Polymer Chemistry, or Material Science/Engineering with 5+ years of related experience, or equivalent, is an asset. Experience with materials used in the medical device industry is an asset. Experience in new product development processes is preferred. A background in polymer chemistry, processes and bulk polymer characterization techniques thereof (Thermal Analyses, Microscopy, Spectroscopy, Chromatography) is required. Must be able to combine characterization methods and/or adapt new methods in order to solve problems. A working knowledge of surface science processes and techniques is an asset. Good communication and presentation skills must be evident; patents, peer review publications and presentations is a plus. Must be able to communicate detailed polymer characterization data to a diverse group of technical and non-technical associates involved in the product development process. Strong interpersonal and leadership skills are essential. Ability to work in team environment, be further mentored by senior scientific fellows, and mentor junior staff members is necessary. This position is located in Somerville, NJ. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	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		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	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	Somerville	NJ	11/19/2009
Regulatory Affairs Specialist
A minimum of a Bachelor's degree in Biology, Biochemistry, Immunology or a related discipline is required. A PhD degree in Biology, Biochemistry, Immunology or a related discipline is strongly preferred. A minimum of 2+ years experience in Regulatory Affairs required. Experience or exposure to the field of Biologics is required. Medical Device and Pharmaceutical experience is an asset. US Regulatory experience is required. EU and International Regulatory experience is an asset. Previous experience in regulations and submitting files for health authorities in Israel is an asset. Excellent communication skills will be necessary for this role. This position will require 10% travel and will be located in Somerville, NJ.
Johnson & Johnson Family of Companies	Salt Lake City	UT	11/19/2009
Salt Lake City, UT: Full Line Sales Representative: Ethicon Endo-Surgery, Inc.
To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as an Associate Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	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	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	Philadelphia	PA	11/19/2009
PA/OH/WV/MD: Territory Manager: Veridex, LLC, a Division of Ortho-Clinical Diagnostics, Inc.
To be considered for this role, candidates must meet the following criteria: A minimum of a BA/BS degree paired with a minimum of 5-10 years of related experience strongly preferred. MBA a plus. Diagnostic field sales experience with an emphasis in the field of oncology and histopathology and technology selling preferred. Advanced knowledge of customer lymph node processes, along with a working knowledge of the appropriate supporting products a plus. Clinical Experience or related activities a plus. Knowledge of Microsoft Word, Excel, Power Point and Outlook required. Valid drivers license issued in one of the 50 States and clean driving record required. Ability to work in an operating room setting. Ability to travel as necessary or required, which may include overnight and/or weekend travel. Excellent written and oral communication skills. Self directed and self motivated, with a proven track record of career success. Ideal candidate will live (or be willing to relocate) in close proximity to a major airport. 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
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	Spokane	WA	11/19/2009
LAB SPECIALIST- Spokane, Washington Area
A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is strongly preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 70% travel will be required for this position. This position will based in Spokane, Washington Area. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Ann Arbor	MI	11/19/2009
Ann Arbor, MI : Full-Line Sales Representative-Core: Ethicon Endo-Surgery, Inc.
To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Albany	NY	11/19/2009
Albany, NY - Full Line Sales Rep - Ethicon-Endo Surgery
To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	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	Athens	GA	11/19/2009
PROCESS DEVELOPMENT CHEMIST (POST-DOC)
Doctoral degree (Ph.D.) in organic chemistry or related field, with 0-2 years of relevant work experience.
Johnson & Johnson Family of Companies	Syracuse	NY	11/19/2009
Syracuse, NY - Full Line Sales Rep - Ethicon-Endo Surgery
To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Garden City	NY	11/19/2009
Long Island, NY: Breast Care Specialist: Ethicon Endo-Surgery, Inc.
To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Baltimore	MD	11/19/2009
Baltimore, MD: Breast Care Specialist: Ethicon Endo-Surgery, Inc.
To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	White Plains	NY	11/19/2009
Westchester, NY- Full Line Sales Rep - Ethicon-Endo Surgery
To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Portland	ME	11/19/2009
Portland, ME- Full Line Sales Rep - Ethicon-Endo Surgery
To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Springfield	MA	11/19/2009
Worcester, MA: Energy Sales Specialist - Ethicon-Endo Surgery
To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Columbia	SC	11/19/2009
Columbia, SC: Breast Care Specialist: Ethicon Endo-Surgery, Inc.
To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	San Antonio	TX	11/19/2009
San Antonio, TX: Associate Sales Representative: Ethicon Endo-Surgery, Inc.
To be considered for this role, a Bachelor's degree is required. The ability to travel as necessary, depending on geography (potentially overnight and/or weekends) and willingness to relocate nationally within the first year of employment is required. Two years of outside selling experience is preferred. Candidates must have a valid driver's license in one of the 50 states and clean driving record, as well as excellent written and oral communication skills. Candidate's must either be in active military service or within 12 months of active service or within 12 months of receiving their college degree. Candidates with documented successful sales performance (high growth, results vs. plan), the ability to target accounts and achieve results through a daily action plan and the ability to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributor reps) and KOLs, is preferred. Self-starters with strong time management and planning skills are also a plus. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Raynham	MA	11/19/2009
Polish Operator Lead
A minimum of a High school diploma, G.E.D. or equivalent required. Vocational designation or training in preferred. A minimum of 3 years of experience working in a machine shop or production line environment, machining precise finished products required. A minimum of 1 year of grinding and/or buffing experience preferred. Experience working in a Medical Device manufacturing environment preferred. Experience working in a Good Manufacturing Practice (GMP) or other regulated environment preferred. Prior experience in a leadership role (i.e. team lead, group lead) preferred. Training experience preferred. Experience working in an environment that has gone through Lean process changes preferred. The ability to drive change as a change agent in a Lean environment required. Basic mechanical skills required. Prior inspection experience required. Knowledge of blueprint reading and geometric tolerance dimensions preferred. Basic computer skills required. Experience collaborating in a team environment required. Ability to communicate effectively (read, write, and speak) in English is required. Must have strong interpersonal skills to work with people of the production floor. Basic math skills, with the ability to add, subtract, multiply, divide, compute percentages and work with decimals required. The ability to perform and record measurements with drop indicators, venires and gauges is required. The ability to stand and/or walk more than 50% of the time is required. Ability to lift up to 25 pounds unaided is required. Must be able to work 3rd Shift (9:30 PM - 6:00 AM, Sunday through Thursday). The ability to work occasional overtime and holidays is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Kansas City	MO	11/19/2009
Kansas City, MO: Full-Line Sales Representative-Core: Ethicon Endo-Surgery, Inc.
To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	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	Birmingham	AL	11/19/2009
Birmingham, AL: Core Sales Representative: Ethicon Endo-Surgery, Inc.
To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as an Associate Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	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, Cell Culture (BetaLogics), 1 of 2
M.S. or B.S. with a minimum of 2 years relevant experience in scientific discipline is required. Extensive experience in cell culture is required. Experience in handling human pluripotent stem cells will be given preferential considerations. Extensive experience in basic analytic skills (e.g., real-time PCR, immunohistochemistry, flowcytometry) is required. The candidate must have strong organizational and interpersonal skills along with excellent oral and written communication capabilities. Must thrive in a team-oriented and entrepreneurial environment. Due to the nature of the cell culture, the candidate must be willing to adopt a flexible work schedule. 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	Skillman	NJ	11/19/2009
Associate Scientist, Cell Culture/Microencapsulation (BetaLogics)
M.S. or B.S. with a minimum of 2 years of relevant experience in a scientific discipline is required. Knowledge of GLP is preferred. Extensive experience in cell culture is required. Experience in handling human pluripotent stem cells will be given preferential considerations. Extensive experience in basic analytic skills (e.g., real-time PCR, immunohistochemistry, flowcytometry) is required. The candidate must have strong organizational and interpersonal skills along with excellent oral and written communication capabilities. Must thrive in a team-oriented and entrepreneurial environment. Due to the nature of the cell culture, the candidate must be willing to adopt a flexible work schedule. Teamwork. Provide guidance to new or junior personnel. May serve as liaison to wider internal or external scientific community.
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	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	Nashville	TN	11/19/2009
Oncology Sales Specialist - Charlotte, NC
Millennium Pharmaceuticals	Cambridge	MA	11/19/2009
Senior Manager, Internal Communications
Millennium Pharmaceuticals	Cambridge	MA	11/19/2009
REGIONAL ACCOUNT MANAGER- SouthEast (FL, PR, GA,AL)
Millennium Pharmaceuticals	Cambridge	MA	11/19/2009
Dir, Regulatory Affairs
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	Cambridge	MA	11/19/2009
Counsel, Pharmaceutical Marketing & Sales Promotions
Millennium Pharmaceuticals	Cambridge	MA	11/19/2009
Associate Director/Director, Molecular Medicine
Millennium Pharmaceuticals	Cambridge	MA	11/19/2009
Sr. Manager, Regulatory CMC
Millennium Pharmaceuticals	Cambridge	MA	11/19/2009
Scientist I/Scientist II, Molecular Technologies
Millennium Pharmaceuticals	Cambridge	MA	11/19/2009
MGR II, REGULATORY AFFAIRS
Millennium Pharmaceuticals	Cambridge	MA	11/19/2009
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
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
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
Senior Scientist- Solid State Method Development
SKILLS/ABILITIES: ? Solid state chemistry applied to pharmaceuticals ? Experimental design and statistical analysis for Analytical Chemistry ? Computer applications and proficiency ? cGMPs, ICH Guidelines and Compendial Requirements ? Project planning and management ? Oral and written communications ? Mentoring of staff PERSONAL ATTRIBUTES: ? Motivated self starter ? Team player ? Ability to lead small scientific group ? Committed to quality ? Well organized, efficient worker ? Good interpersonal skills ? Good problem solver ? Creative, innovative thinker ? Developer of people ? Easily adaptable to change ? Brings closure to work in a timely manner EDUCATION AND EXPERIENCE: PhD in Chemistry or materials science in related field with 7+ years of experience, Masters Degree in Chemistry with 10+ years of experience, or Bachelors Degree in Chemistry with 12+ years of experience or equivalent. Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline. Vertex Pharmaceuticals
Vertex Pharmaceuticals	San Diego	CA	11/19/2009
Temporary Scientific Associate (Analytical Development)
* Requires a BS degree in Chemistry and 5+ years of relevant experience or MS degree in Chemistry and 3+ years of relevant experience. * Must have analytical chemistry experience in a pharmaceutical or related field. * Must have experience using HPLC/GR instruments. * Chemical Manufacturing & Control (CMC) environment experience is highly preferred. * Highly self-motivated, you must have good communication skills both written and verbal, be able to multitask, be flexible and have the ability to work in a flexible cross-functional team environment. Vertex Pharmaceuticals
Vertex Pharmaceuticals	San Diego	CA	11/19/2009
Scientist I (Analytical Development)
· Requires a PhD degree in Chemistry and 1+ years of relevant experience; or MS degree in Chemistry and 3+ years of relevant experience; or a BS degree in Chemistry and 6+ years of relevant experience. · Must have a natural products, analytical chemistry or synthetic organic chemistry background. · Strong knowledge of modern analytical chemistry techniques including separation techniques and mass spectrometry experience is required. · Familiarity with Agilent and Thermo Mass spectrometry instrumentation and software is desirable. · Previous pharmaceutical industry experience would be preferred. · Must be highly self-motivated, highly productive with strong problem solving skills and be capable of working both independently and in a collaborative interdepartmental setting. · Strong written and verbal communication as well as interpersonal skills are a must. 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
Sr Scientific Associate, Analytical Development
- A Master's or Bachelor's degree in the life sciences or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry - 0 - 4 years of academic experience in a chemistry or analytical chemistry laboratory setting with some previous related industry experience preferred - Familiarity with, or a desire to gain a working understanding of, HPLC, LC-MS, GC, GC-MS, FT-IR, UV-VIS, KF and other instruments used in the analysis of pharmaceutical products - An interest in and passion for establishing a career in analytical development and the biopharmaceutical industries - The ability to work successfully in both a team environment as well as independently - Excellent written and verbal communication skills - Established organizational skills Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline. Vertex Pharmaceuticals
Vertex Pharmaceuticals	Cambridge	MA	11/19/2009
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	San Diego	CA	11/19/2009
Research Scientist II (Medicinal Chemistry)
Minimum Requirements ? Ph. D. in organic synthesis with 2-5+ years of productive, relevant post-doctoral experience or ? MS in organic synthesis with 5+ years of productive pharmaceutical experience or ? BS in organic chemistry with 8+ years of productive pharmaceutical experience Vertex Pharmaceuticals
Vertex Pharmaceuticals	San Diego	CA	11/19/2009
Research Scientist I (Medicinal Chemistry)
Minimum Requirements ? Ph. D. in organic synthesis with 0-3 years of productive, relevant post-doctoral experience or ? MS in organic synthesis with 3+ years of productive pharmaceutical experience or ? BS in organic chemistry with 6+ years of productive pharmaceutical experience 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.	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.	Santa Monica	CA	11/19/2009
Associate Director/Director, Toxicology- Agensys, Santa Monica, CA
? Ph.D in toxicology, biochemistry, pharmacology, pharmacokinetics or related sciences; minimum of 10 years of pharmaceutical industry, including 7 years in toxicology and management experience ? Comprehensive knowledge of drug development (non-clinical and clinical) ? Experience with non-clinical CROs ? Knowledge and experience in biopharmaceutics, toxicology, toxicokinetics, ADME and pharmacokinetics with therapeutic antibodies and antibody drug conjugates ? Knowledge of FDA regulations pertaining to non-clinical and clinical drug development. ? Well developed oral and written communication
Astellas Pharma, Inc.	Deerfield	IL	11/19/2009
Associate Director, Pharmacovigilance QA Lead
1. Minimum B.A/B.S. in science (biology, chemistry, pharmacy) or relevant related field of study. 2. Minimum of 5-to-9 years experience in pharmaceutical or biotechnology industries, including safety quality assurance and management experience 3. Ability to work independently and also within teams are essential4. Ability to travel up to 20% domestically and/or internationally 5. Working knowledge of FDA and international regulations (e.g., Volume 9a) 6. Ability to interact and communicate effectively with various levels of management. 7. Excellent communication and project management skills 8. Computer skills to include Microsoft Office (Power Point, Visio, Excel), Access and Project 9. Excellent facilitation, negotiation, problem-solving, and conflict resolution skills 10. Initiates and maintains extensive contacts within both internal and external networks 11. Excellent oral and written communication skills including the ability to present formally and informally within area of expertise to a diverse set of audiences, including senior management and external customers
Astellas Pharma, Inc.	Deerfield	IL	11/19/2009
Assistant Director, Advertising and Promotion Review
1. Bachelor's degree in scientific discipline; advanced degree preferred2. At least 8 years previous industry experience; 5 in RA. Scientific knowledge in chemistry, general biological/physical science and ability to apply that knowledge to regulatory issues and product development having technical complexity. 3. Direct advertising and promotional material review experience required.4. Able to communicate effectively and maintain effective working relationships. Must be able to effectively influence peers and others within the organization.5. Proven ability to prioritize and multi-task with minimal supervision based on interactions with project team members.6. Excellent written and verbal communication skills (native and non-native English speakers) with the ability to meet regulatory requirements and standards while maintaining effective relationships.7. Strong organizational skills and high level of attention to detail, with the ability to coordinate multiple large and diverse projects simultaneously
Astellas Pharma, Inc.	Deerfield	IL	11/19/2009
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.	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.
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.	RTP	Durham	11/19/2009
Chemical Engineer
This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001968. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Chemist
This position requires candidate to be currently enrolled in a BS program in Chemistry or Biochemistry. Ideal candidate will possess superior communication and interpersonal skills. Laboratory experience is preferred. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002018. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Merck Manufacturing Development Program
This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Mechanical Engineering, Industrial Engineering, Chemistry/ Biochemistry, Biology/ Microbiology, or Supply Chain Management. Ideal candidate will possess superior communication and interpersonal skills, a team player with the ability to work independently. Must be graduating between August 2009 and August 2010. Must be willing to be assigned to different jobs and potentially different sites over the first two years of employment. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002036. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Merck Technical Rotation Program
This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Chemistry/ Biochemistry, Biology/ Microbiology. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002035. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Staff Chemical Engineer
This position requires candidate to be currently enrolled in a MS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002019. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Senior Chemical Engineer
This position requires candidate to be currently enrolled in a PhD program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002024.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Senior Chemist
This position requires candidate to be currently enrolled in a PhD program in Chemistry or Biochemistry. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002034.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Chemical Engineer
This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001998. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Chemical Engineer
This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001988. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Chemical Engineer
This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001978. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Manufacturing Development Program
This position requires candidate to be currently enrolled in a MS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Mechanical Engineering, Industrial Engineering, Chemistry/ Biochemistry, Biology/ Microbiology, or Supply Chain Management. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002049. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003868. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003878. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003888. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003898. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003908. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Merck Manufacturing Science Intern
This position requires applicant to be currently working toward a Bachelors degree in Biology, Microbiology, Virology, Chemistry or Biochemistry. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ADM003932 Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003918. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003928. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Merck Manufacturing Science Intern
This position requires applicant to be currently working toward a Bachelors degree in Biology, Microbiology, Virology, Chemistry or Biochemistry. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ADM003942. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Merck Manufacturing Graduate Intern
This position requires applicant to be currently working toward a working toward graduate degree in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Statistics or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000318. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Senior Research Chemist (Continuous Recruitment)
Required PhD in Chemistry or Biochemistry is required. Degree completion no later than end of 2010 required. DesiredSome relevant experience via a co-op, internship, or independent research is preferred for consideration. If you, like us, strive for excellence in all you do, consider joining our team of talented and dedicated individuals from diverse backgrounds who are united in bringing Merck's finest achievements to people around the world. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers/university/ to create a profile and submit your resume for requisition # CHE002098. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.
Merck & Co., Inc.	West Point	PA	11/19/2009
Chemical Engineer
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002008. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Whitehouse Station	NJ	11/19/2009
MMD MS Chemistry College Recruiting
QualificationsThis position requires candidate to be currently enrolled in a MS program in Chemistry or Biochemistry. Ideal candidate will possess superior communication and interpersonal skills. Laboratory experience is preferred. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002122.
Merck & Co., Inc.	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.	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.	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 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
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.	West Point	PA	11/19/2009
Site Compliance Specialist
Education:A Bachelor of Science in a life science (such as Biology, Chemistry, etc.) or an appropriate Engineering field is required; candidates with majors in other fields will not be considered. A major in Biology, Microbiology, Biochemistry, Virology, or Engineering is preferred. Required:At least two (2) years of experience, in broad based quality control and/or quality assurance audits or inspections, or other experience in a variety of manufacturing, packaging, testing, or technical support areas. Desired:Experience in bulk vaccine manufacturing or other bulk vaccine support area is desirable. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001929. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	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.	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
Staff Biochemist
Education Minimum Requirement: Master's Degree or a Bachelor's degree with a minimum 2 years of industry experience Required Experience and Skills: Experience with mammalian cell culture and cell-based potency assays, both on a large scale Basic knowledge of MS Word and Excel Desired Experience and Skills: Experience with automation, ie Backman instrumentation Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # BIO002470. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	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.
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	MA	11/20/2009
TS - Strategic Projects Leader
Ideal Background: Education (minimum/desirable): PhD, MD or PharmD level scientist or life science background with at least 5 years relevant experience. MBA is preferred. Languages: Fluent oral and written English Experience/Professional requirement: 1. Strong knowledge of both early and late phases of pharma-ceutical drug development 2. Proven team leadership skills on complex projects 3. Ability deal with project start-up activities and implementa-tion 4. Excellent communicator ? good presentation and strong medical / scientific writing skills 5. Excellent team work in a multidisciplinary environment 6. Excellent organizational skills, as well as predisposition for innovation 7. Recognized for combining operational and scientific excel-lence in Drug Development
Novartis Oncology	na	NC	11/20/2009
Technician II, Lab
EDUCATION/EXPERIENCE: High school diploma or equivalent required. Degree in physical sciences, statistics, or mathematics preferred. 3-5 years in a fast paced pharmaceutical environment and background in stability, statistics, chemistry or chemical analysis of pharmaceutical finished product dosage forms preferred.
Novartis Oncology	na	CA	11/20/2009
Technical Manager CMO - Emeryville, CA
-Degree in related technical field (Biotechnology / Chemical Engineering / (Bio)chemistry) with doctorate (PhD) desirable or appropriate combination of education and experience. -English fluent spoken and written; German & French spoken are a clear ?plus? -Minimal 7-10 years confirmed experience in biotechnology manufacturing, ideally with direct responsibilities in manufacturing operations, 3rd-party management, toll-manufacturing activities or related area; Microbial expression system manufacturing background a plus.
Novartis Oncology	na	NJ	11/20/2009
Sr.Regulatory CMC Liaison Manager
Education and/or Professional Experience: Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent. Desirable: Advanced degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent. Languages: Fluent English required (oral & written). Good skills in site (local) language desired (oral). Experience/Professional Requirements: 6-8 years in regulatory preferred, and/or experience in drug/biologic pharmaceuticals Working knowledge/experience in regulatory submission and approval processes for New Chemical Entities (NCE) and product life cycle management and proven practical knowledge of and ability to deal with complex CMC regulatory issues and requirements. Proven track record of successfully working in interdisciplinary teams, and of planning, coordinating and leading activities simultaneously on multiple projects. Regularly demonstrated active contributions to line functions or project teams, as well as ability to contribute to matrix teams with the necessary strategic thinking. Demonstrated ability for strategic thinking, maintaining awareness of business impact. Demonstrated ability for risk assessment and mitigation. Computer literacy (e.g. MS-project, Power Point, document management systems) available and shown ability to quickly learn new software and tracking tools and associated processes. Strong interpersonal, communication, negotiation and problem solving skills.
Novartis Oncology	na	NJ	11/20/2009
Sr. 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	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	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 Scientist (Pharmacokinetics)
M.S. degree in biological or related sciences with minimal 3 years laboratory experience. Research experience using animal models is mandatory. Small animal surgical experience is highly desired. Excellent verbal and written communication skills are essential. The knowledge of radiochemistry, tissue distribution, metabolism and pharmacokinetics is desirable. Prior work experience with PK/PD analysis and a demonstrated ability to work with modeling tools and databases (e.g. WinNonlin, GastroPlus, Watson, Spotfire, etc) is a plus. THIS REQUISITION APPROVED BY TSLT ON 1-JULY-2009 AND MOVED TO CRITICAL HIRE LIST.
Novartis Oncology	na	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
Scientist, Pharmacokinetics
EDUCATION/EXPERIENCE: Ph.D. with 1-3 years or MS with 5-8 years of experience in one or more areas biopharmaceutics, pharmacokinetics, drug metabolism, bioanalytical chemistry, biostatistics, PK modeling, in vivo-in vitro correlation (IVIVC), and clinical endpoint BE study design/conduct. Inhalation experience a plus.
Novartis Oncology	na	NJ	11/20/2009
Scientist, NPKPD
M.S. degree in biological or related sciences. Research experience using animal models is mandatory. Small animal surgical experience is highly desired. Good verbal and written communication skills are essential. The knowledge of radiochemistry, tissue distribution, metabolism and pharmacology is desirable. Prior work experience with PK/PD or statistical analysis and a demonstrated ability to work with modeling tools and databases (e.g. WinNonlin, GastroPlus, Watson, Spotfire, etc) is a plus.
Novartis Oncology	na	MA	11/20/2009
Scientist-Biochemical & Organ Toxicology
Technical Skill Sets ? Good skills in isolating and cultivating cells from different organs in different species ? Good skills in performing a variety of biochemical techniques (e.g., preparation of cell and tissue extracts, subcellular fractionation, enzyme assays, ELISA, Western blots, ?). ? Good skills in performing a variety of molecular biology techniques (e.g. nucleic acid purification, cloning, PCR) ? Good understanding of SOPs as well as their practical implementation ? Fluency in English ? Working knowledge of relevant IT systems Experience ? At least 3 years of experience in cellular biology or toxicology in either academic or industrial environment ? Working experience with mammalian cell culture models (primary cultures and cell lines) and related techniques ? Working experience in molecular & biochemical analytical techniques Personal Skill Sets: ? Interpersonal and teamwork skills ? Good oral communication and writing skills ? Computer skills for experimental organization, assay design, data collection and analysis, and report writing Education Bachelor or Master degree in life sciences, preferably biochemistry, pharmacology or biology.
Novartis Oncology	na	MA	11/20/2009
Scientist 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
Scientific Education Manager, Chemistry
PhD in chemistry with 3-5 years of experience in pharma/biotech as a medicinal chemist. Experience in scientific education, web-based learning tools, DMPK, or pharmacology 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 HSE Risk Manager
This position requires 3-5 years experience in health, safety, and environmental risk assessment and management in a biotech/ pharma laboratory environment. The successful candidate should have experience in implementation and maintenance of HSE audit systems, development of tools and programs, and will have conducted periodic audits and follow up for corrective measures. Bachelor degree in life sciences, chemistry, or other appropriate discipline and ABSA certification as a Certified Biosafety Professional (CBP) or other equivalent certification in Occupational Health and Safety Program is required. Solid verbal and written English communication skills. Fluency in additional languages, such as German or Mandarin would be favorably considered. Demonstrated leadership abilities, as well as the ability to communicate and influence others in a complex, matrixed environment are essential.
Novartis Oncology	na	MA	11/20/2009
Research Associate ? X-ray crystallography
B.S/M.S. or equivalent in biochemistry or a related discipline with at least 2 years of research laboratory experience. Experience in protein chemistry (e.g. expression, purification and characterization) is required. Experience with protein crystallization, x-ray data collection, and/or biophysical characterization of proteins would be a decided asset. The candidate must possess good oral and written communication skills.
Novartis Oncology	na	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	MA	11/20/2009
Research Associate - Bacteriology/Biochemistry
The ideal candidate will have a BSc/MSc degree in molecular biology or biochemistry and several years of relevant industry experience within an infectious diseases context.
Novartis Oncology	na	NJ	11/20/2009
Regulatory CMC Liaison / Biologics
Minimum: Relevant scientific degree in biotechnology, biochemistry and cell biology or equivalent. Languages: Fluent English required (oral & written). Experience / Professional Requirements: ? Several years of experience in regulatory preferred. ? Excellent working knowledge/experience in regulatory submissions and approval processes for Biopharmaceuticals and ability to deal with complex CMC regulatory issues and requirements ? Strong background in biopharmaceutical development (e.g. cell culture, downstream processing, analytics). Biologics experience desired ? Proven track record in successfully leading/working in interdisciplinary teams, and of planning, coordinating and leading activities simultaneously on multiple projects. ? Strong interpersonal, organizational, communication, presentation, negotiation and problem solving skills.
Novartis Oncology	na	NC	11/20/2009
QC Chemist IV
EDUCATION/EXPERIENCE BS or BA in Chemistry or life sciences and 8 or more years of professional related
Novartis Oncology	na	NJ	11/20/2009
Principal Scientist (GMP Facility Manager/Engineer)
Education Minimum: BS/MS or equivalent with greater than 8 years of experience. Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent) with a minimum of 5 years of experience. Languages: Fluent English (oral and written) Experience/Professional Requirement: 1. Successfully demonstrated several years (minimum of 3 years) of directly related experience as senior scientist of Ph.D. with post-doctoral/industrial experience (minimum of 1 year) or equivalent. 2. Successfully demonstrated expertise in a specific scientific/technical area. 3. Recognized achievements in the development of new lab/plant procedures. 4. Excellent knowledge of laboratory and/or technical tools. 5. Proficient in utilization of special tools/equipment, lab automation tools and specialized facilities e.g., containment/sterile labs. 6. Thorough understanding of development activities and processes in a specific function. 7. Good knowledge of software and computer tools. 8. Profound literature search skills. 9. Good presentation skills and scientific/technical writing skills. 10. Strong scientific leadership skills. 11. Strong knowledge of relevant SOP, GLP, GMP and Novartis regulations and policies.
Novartis Oncology	na	MA	11/20/2009
Presidential Post Doctoral Fellow
Multiple positions exist at all sites of Novartis Institutes for BioMedical Research for individuals with the following minimum requirements: Ph.D. in biological sciences, chemistry, or computer science. Applicants who have commenced postdoctoral training may apply as well, but they should not have been in postdoctoral training for more than 3 years. Candidates must be able to work independently and also participate in team efforts. Excellent oral / written communication and presentation skills and scientific creativity are essential.
Novartis Oncology	na	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
The candidate should have a PhD. with 3+ years of experience in the pharmaceutical or biotech field,experience with developing new assays and transitioning them to HTS and a strong understanding of cellular biology and its relationship to cancer indications is a must. The ability to analyze large datasets for statistically relevant information, and experience with multiple automation platforms also required.
Novartis Oncology	na	MA	11/20/2009
PhD Medicinal/Synthetic Organic Chemist
* Ph.D. in synthetic organic or medicinal chemistry * 2-6 years of relevant post doctoral or industrial experience * Experience managing BS/MS chemists * Proven track record of innovative project contributions including peer-reviewed publications * Ability to work independently and ability to interact with a multidisciplinary team of medicinal chemists, biologists, pharmacologists and external collaborators. * Experience with modern structure-based drug design and multi-parallel synthesis is a plus. * Excellent oral / written communication and presentation skills * Flexibility to work in a dynamic environment
Novartis Oncology	na	MA	11/20/2009
Pharmacogenetic Analyst (CP)
Competencies: ? Strong background in genetics and/or molecular biology ? Previous experience performing genetic association studies required ? Strong background in biostatistics and/or statistical genetics ? SAS programming a plus ? Proficiency working with and manipulating large data sets ? Broad scientific knowledge ? Experience in clinical development desirable ? Ability to work well in a team environment ? Excellent presentation and communication skills (essential) ? Strong publication record desirable Education and professional experience: PhD in genetics (or related fields) is required with experience performing genetic/genomic association studies.
Novartis Oncology	na	MA	11/20/2009
Ph.D Scientist: Oncology Biotherapeutics
Biotherapeutics lab head Qualifications: ? Ph.D. molecular biology or related field. ? Minimum 3 years of post-doctoral experience in cancer and/or antibody therapeutic research. ? Independent, self motivated and innovative personality ? Excellent written and oral communication skills ? Extensive experience in cell and biochemical assay development and analysis
Novartis Oncology	na	MA	11/20/2009
Pathways Research Scientist (BS/MS)
?BS or MS in Biochemistry, Molecular Biology, or Cell Biology, with 5+ years of laboratory research experience. ? Extensive experience with culturing various mammalian cell lines, utilizing both 2D and 3D culture systems, designing cell-based assays, generating stable cell lines, and executing small molecule screens with laboratory automation equipment. ? Experience with high content imaging and designing/executing high content imaging-based screens. ? Outstanding molecular biology techniques including complex DNA cloning, site-directed mutagenesis, and qPCR. ? Exceptional expertise in genetic screening with siRNA/shRNA/cDNA by conventional and viral transduction technologies. ? Proficient in various protein analysis techniques, including, but not limited to, ELISA assays, immunoprecipitations, and western blots. ?Excellent communication skills
Novartis Oncology	na	MA	11/20/2009
Patent Attorney, Chemistry
Minimum education: B.A., B.Sc. (or equivalent) , chemistry, biochemistry or equivalent with strong understanding of medicinal chemistry in a biotech/ pharma environment. M.S., Ph.D. or equivalent in organic or medicinal chemistry preferred. J.D. or equivalent; Admission to at least one state bar; and Registered to practice before Patent Office. ?Expertise in local patent law; Detailed understanding of global patent systems (including but not limited to US, EP, JP and international systems), patent process, documentation and national and international patent office filing systems. ?Strong scientific background. ?Strong customer-service focus to build and sustain good working partnerships with key stakeholders and project teams. ?Effective analytical, presentation and communication skills. ?Demonstrated ability to work independently as well as collaboratively in a team. ?Well-developed research and critical thinking skills, and sound decision-making abilities, with attention to detail to produce consistently accurate work. ?Strong organization and time management skills with flexibility, creativity, resourcefulness to successfully prioritize and manage multiple, competing priorities simultaneously. ?Strong written and spoken communication in English is required. Proficiency in other languages, such as German, a plus.
Novartis Oncology	na	MA	11/20/2009
Oncology Pharmacology PhD- PK/PD
A PhD degree in one of the life sciences, with expertise in in vivo physiology or pharmacology and at least three years postdoctoral and/or industry experience. Industry experience with oncology models is strongly preferred. The candidate should have a comprehensive, in-depth knowledge of Oncology research, particularly related to industrial drug discovery and development, with emphasis on drug combinations. He/she should have a strong background in molecular biology, biochemistry, developmental biology and a good knowledge of statistics. The candidate is also expected to be highly motivated, to have excellent leadership, communication and inter-personal skills. Experience in leading Oncology drug discovery programs and/or supervisory experience is a plus.
Novartis Oncology	na	NJ	11/20/2009
Oncology Global Drug Development Fellow
Qualifications required Medical Doctorate (MD) degree or equivalent is required. Advanced knowledge in Oncology, Haematology, Endocrinology required. Completion of 2-4 years of post-MD training in above area required. Fluent oral and written English. Any other language a plus. Knowledge, Skills, and Experience desired Involvement in patient care and demonstrated medical/scientific expertise in oncology and/or haematology Exposure to or demonstrated interest and knowledge in pharmaceutical company research environment Strong interpersonal, communication, and problem solving skills. Demonstration of general understanding of drug development process including key processes involved in protocol development, clinical trial conduct, statistical analysis of trials, and regulatory environment, Demonstration of ability to work within a team environment and across other functions Mobility/Citizenship Must be able to relocate to Basel, Switzerland or New Jersey, USA for a period of one year Current residency/citizenship of an EU country is highly preferred. Must be able to attain the appropriate work authorization for the US in a timely fashion. For US and Switzerland, Novartis will apply on the candidate?s behalf.
Novartis Oncology	na	WA	11/20/2009
Oncol Area Sales Manager/Sr Area Sales Manager
Bachelor's degree required with a minimum of three years of pharmaceuticals sales management experience in the oncology, institutional, or specialty marketplace. Qualified candidates must have a demonstrated record of success in their ability to lead and inspire a sales team towards meeting and exceeding objectives, to communicate and implement tactical product strategies with a sophisticated audience, and to think strategically (i.e., "outside the box" and look at the "big picture") while providing creative and innovative solutions to market problems. Personal integrity and leadership abilities are essential. Excellent interpersonal, communication (both written and verbal), and presentation skills are required. Must be able to effectively multitask, problem-solve, and make decisions. Computer literacy (i.e., Word, Excel, and PowerPoint) is a must. As one of the largest pharmaceutical companies in the world and voted as one of the 100 Best Companies to work for by Working Mother Magazine, we are committed to peak performance, improving the quality of life, and embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V
Novartis Oncology	na	NJ	11/20/2009
Onco Dir Clinical Rsch Phys
? MD or PhD in Clinical Parmacology, Biochemistry or related field ? Substantial postgraduate bedside or clinical pharmacology experience in a relevant cancer treating discipline and institution required. ? Substantial experience with determining, administering, and evaluating the outcome of systemic combined modality cancer or adult hematologic malignancy treatment plans required. ? ? 3 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV. ? Medical/scientific and operational expertise in cancer molecular medicine, biologics, and or response modifiers ? Demonstrated technical knowledge and innovation in early clinical development study designs that provide relevant evidence to decision-makers. ? Versatile knowledge and understand of pre-clinical science of oncology and all aspects of translational medicine such as toxicology, pharmacology, and regulatory requirements for early phase development in at least two relevant jurisdictions
Novartis Oncology	na	MA	11/20/2009
MS/ Ph.D Oncology Drug Discovery/ Target Validation Research Associate
The ideal candidate should possess a MS degree with 3-5 years of relevant biotech research experience. Candidates with a tumor biology Ph.D and relevant technical skills who are looking for a non-supervisory, technically driven position, are also encouraged to apply. Knowledge of cell signaling pathways as related to oncology or other proliferative diseases is crucial. It is essential that you have an excellent working knowledge of a breadth of cellular and molecular biological methods (especially RNAi, RT-qPCR, cloning, cell culture, transient/ stable cell line generation, immuno-detection and phenotypic characterization). You should be a scientifically motivated self starter, capable of independently conceiving, conducting and critically analyzing your own innovative research with minimal supervision. Strong presentation skills, communication and the ability to work in a fast-paced team-oriented environment will also be vital.
Novartis Oncology	na	MA	11/20/2009
Molecular/Cellular Biology Research Scientist (BS/MS)
B.S or M.S scientist with at least 3 years of relevant research experience; the candidate has strong background in cellular and molecular biology. Previous experience in the study of innate immunity is highly desirable; experience in cellular immunology and in vivo biology is advantageous. Experience with large dataset analysis is a plus. The candidate is expected to possess strong problem solving and analytical skills, and be capable of independent thinking. Excellent communication and organization skills are required.
Novartis Oncology	na	MA	11/20/2009
Molecular Pathways Investigator (Ph.D)
Ph. D. degree with 1- 3 years of postdoctoral training and with strong background in cell biology, biochemistry and molecular biology. Previous experience with identification and progression of biological targets is a plus. The candidate is expected to possess strong problem solving and analytical skills, and be capable of independent, creative thinking. Excellent communication and organization skills are required.
Novartis Oncology	na	MA	11/20/2009
Molecular Pathologist
Education: DVM or MD, board-certified pathologist, MSc Experience: Scientific experience and/or training as a molecular pathologist Technical Ability: Technical and scientific experitise in ISH, IHC, immunofluorescence and knowledge in various aspects of molecular biology. Scientific experience in the development of novel protein and nucleic acid detection methods applied to tissue sections Presentation: Good oral and written communication skills. Able to present data to peers and senior colleagues
Novartis Oncology	na	MA	11/20/2009
Medicinal Chemistry Associates/Scientists (BS/MS)
Multiple positions exist at all levels for candidates with the following minimum qualifications. B.S. in Chemistry or M.S. degree with at least 1 year experience in the synthesis and characterization of organic compounds. Experience with common spectroscopy (NMR, IR, UV, MS) and analytical techniques required. Experience with chromatography purification systems required. Good written and oral communication skills are required for effective drug discovery team participation. For faster consideration, please provide research summary when submitting resume. NIBRIERP
Novartis Oncology	na	CA	11/20/2009
Manager Quality Assurance-CMO (Emeryville, Calif)
-Bachelor or higher in Biochemistry, Chemistry, Microbiology or another related science -Fluent in speaking / writing in English -7 to 10 years experience in the pharmaceutical industry, with direct experience with Biopharmaceutical APIs. Experience in QA Operations, production, QC and/or other relevant operational areas, but must include minimally 5 years in QA, and 3 years of management and or project management experience.
Novartis Oncology	na	MA	11/20/2009
Lab of the Future (LOTF) Project Manager
Advanced degree in a scientific (biology or chemistry) discipline. MBA is a plus. Project management proficiency and experience in biotech/pharma required. Excellent communication, presentation and written skills in English are essential; German or Mandarin a plus. ?Generally proficient with design, business, and science concepts in order to better collaborate with scientists, architects, IT professionals, etc. ?Proven ability to set and meet performance targets within a predefined budget and timeline ?Excellent understanding of laboratory environments ?Ability to work collaboratively with and influence multiple stakeholders and users ?Excellent command of Microsoft Office ?Comfort with ambiguity ?Demonstrated ability to innovate ?Results driven ?Highly committed and self-disciplined
Novartis Oncology	na	MA	11/20/2009
Lab Head, Antibody & Protein Structure
This role requires a PhD in Biochemistry, Molecular Biology or Structural Biology and a minimum of 2-3 years of relevant post-doc experience in antibody/protein structure study. A strong team-working focus and excellent communications and inter-personal skills. A proven scientific track record in the design and engineering of therapeutic antibodies and proteins.
Novartis Oncology	na	MA	11/20/2009
Lab Head, Antibody & Protein Design, Novartis Biologics
This role requires a PhD in Biochemistry, Molecular Biology or Immunology and a minimum of 3 years of relevant post-doc experience. Strong team-working focus and excellent communications and inter-personal skills. Strong proven scientific track record in the discovery and engineering of therapeutic antibodies and proteins. The role is located in Cambridge, MA and reports to the Unit Head of Protein Design.
Novartis Oncology	na	MA	11/20/2009
IT Application Management
-BS Degree in Computer Science or equivalent preferred -6 years or more experience to include service delivery & management of document/records management systems -Strong Documentum 6.5 (WebTop, BPM, BPI, DTS/CTS) -Strong Java background -Strong Web Application background (Tomcat, JBoss) -Strong ITIL Service Management -Medium Project Management -Scientific background preferred
Novartis Oncology	na	MA	11/20/2009
Innate Immunity/TLR Biology Investigator (Ph.D)
Ph. D. degree with 1- 3 years of postdoctoral training and with strong background in cell biology, biochemistry and molecular biology. Previous experience in the study of innate immunity including inflammasome is highly desirable. Experience with large dataset analysis is a plus. The candidate is expected to possess strong problem solving and analytical skills, and be capable of independent, creative thinking. Excellent communication and organization skills are required.
Novartis Oncology	na	MA	11/20/2009
Histotechnology Research Scientist (BS/MS)
The ideal candidate will have a BS or MS degree in a biological or chemical science discipline plus at least 4 years of histology experience. Strong organizational skills, self-motivation, attention to detail, flexibility, proactive willingness and desire to engage in the laboratory workflow, and an ability to contribute to a team environment are essential. Candidates should have experience working in a fast-paced, high volume, high productivity and quality environment, in either an industry or clinical laboratory. Experience and proficiency with immunohistochemistry methodology and image analysis is strongly preferred. Prior experience in cell biology and/or molecular biology techniques is preferred.
Novartis Oncology	na	WA	11/20/2009
Hematology Sales Representative/Specialist - Spokane, WA
Bachelor?s Degree 5 years of pharmaceutical sales experience At least 2 years of experience in oncology/urology/institutional/specialty sales. Computer literacy i.e., Word, Excel, PowerPoint Candidates must be self-motivated, possess a high degree of technical expertise, have exceptional selling skills, be team-oriented and must be familiar with the Oncology community. Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V.
Novartis Oncology	na	MA	11/20/2009
Head of Engineering
BS/MS (PhD preferred) in Engineering (Biomedical/ Bioengineering, Mechanical, Electronic, Chemical, Systems) with minimum of 7 years experience in Life sciences or medical device development. English In vitro molecular diagnostics experience essential. Familiar with regulatory and compliance requirements for diagnostic tests. Experience in engineering design, optics, hardware, system architecture, application support, and disposables. Minimum 2 years in role as systems engineer or system analyst. Experience working on multi- disciplinary projects. Strong knowledge of assay chemistry for diagnostic tests/ molecular biology. Excellent oral and written communication skills with the proven ability to work effectively across a matrixed and widely dispersed organization. Ability to lead and succeed in a multi-cultural environment.
Novartis Oncology	na	MA	11/20/2009
Head of Bioinformatics & Biostatistics
Education: Minimum ? MS, Desirable - PhD Experience: Minimum - 8 years , Desirable ? 10 years. Management experience: Minimum ? 4 years, Desirable ? 6 years. In vitro diagnostics experience essential. Specific Professional Competencies: - Must have proven proficiency in common statistical and data mining techniques used in analyzing biological data. - Must have experience using R, Matlab, Spotfire, Partek or similar data analysis software. - Proficiency in developing applications in high-level (Java, C++, C#) and scripting (Perl, Python, Ruby) programming languages to accomplish bioinformatics tasks. Familiarity with web frameworks such as Rails or Django is highly desirable. - Experience using relational databases such as SQL Server, Oracle or PostgreSQL - Knowledge of bioinformatics tools and databases such as the NCBI and UCSC Genome Browser, BLAST, Primer3, GEO and BioConductor - Knowledge of pathway analysis and tools such as Ingenuity Pathway Analysis and GeneGo?s MetaCore is highly desirable. - Familiarity with assay development and common laboratory techniques is highly desirable. - Good understanding of molecular biology and diagnostic development is highly desirable. - Must have excellent communication and presentation skills.
Novartis Oncology	na	MA	11/20/2009
Group Head, Biochemical & Organ Toxicology (Cambridge)
We are seeking an experienced scientist and manager to lead a Biochemical & Organ Toxicology group within Investigative Toxicology (Preclinical Safety, Translational Sciences) based in Cambridge, MA. Investigative Toxicology is using non-clinical innovative investigations to discover the mechanisms of target organ toxicity and to prevent and solve pre-clinical and clinical drug safety issues. The candidate will be responsible for the design and set-up of new experimental facilities for 3 laboratories, and the management of staff therein. The candidate will also be responsible for subsequent development, implementation and management of experimental studies. The primary deliverable of these laboratories (Endocrine & Repro-toxicology, Protein & Mitochondrial Toxicology and Biochemical & Cellular Toxicology) will be to facilitate the early identification and characterisation of toxicities during preclinical phases of drug development with a particular focus on Novartis Institute for Biomedical Research (NIBR) disease areas, expertise and technologies in Cambridge. In addition, the candidate will also work closely with Preclinical Safety Project Team Representatives to help assess potential safety liabilities associated with novel drugs and their target(s). The candidate will report to the Global Head of Biochemical and Organ Toxicology and will interact closely with colleagues in other groups as a member of cross-functional and multi-disciplinary teams (including global Investigative Toxicology & Preclinical Safety departments, NIBR and external collaborators).
Novartis Oncology	na	MA	11/20/2009
Global Program Diagnostics Director
Education: Doctoral in life sciences or chemistry, or MBA with equivalent experience in life sciences. Languages: Fluent English (written and oral), on other language Experience/Professional Requirement: 1. 12+ years industry experience 2. 5+ years multi/cross functional leadership experience 3. International drug or diagnostic development project functional leadership 4. Have an advanced understanding of the diagnostic development process and programs. 5. Provide thought-leading insights to the competitive environment and internal partner interfaces 6. Sound knowledge of international customs and business practice 7. Hands on experience with a major submission and regulatory review process 8. Proven people leadership capabilities 9. Model natural leadership characteristics 10. Expert leadership skills demonstrated in GPT, in staff management role or in other organisational assignments. Expert skills to facilitate/optimise contribution of team members as individuals and members of cohesive team. 11. Strong interpersonal and communication skills for bridging scientific and business participants, for negotiating timelines and for effective international collaboration. 12. Outstanding verbal and written communications. 13. Diagnostic or therapeutic experience is an advantage
Novartis Oncology	na	MA	11/20/2009
Fellow, Endocrine and Reproductive Toxicology (Cambridge)
Minimum Requirements ? Ph.D. degree in Biochemistry, Physiology, Cell Biology, Toxicology or a related Biological Science. ? At least 2 years of prior experience in pharmaceutical drug development and/or toxicological sciences is required ? A strong expertise in hormonal disruption and toxicology, and reprotoxicology ? Experience of managing highly skilled technical staff, laboratory equipment, consumables and safety is desirable. ? Fluency in English (written and spoken) is a must. ? Flexibility and ability to work in a team, comfortable with multitasking, good written and oral communication skills, independent and accurate working style, ability to plan and organise effectively, willingness to take on additional responsibilities are expected.
Novartis Oncology	na	MA	11/20/2009
Facilitators for pharmaceutical teams curriculum
Experienced Facilitators with references needed.
Novartis Oncology	na	NJ	11/20/2009
Expert Clinical Manager
Phase I Oncology clinical trial experience a requirement. On an exception basis highly-qualified candidates with strong oncology experience with Phase 2/3 clinical trial experience might also be considered. Candidates should have 3-5 years of experience in clinical environment (at least 2+ pharma. industry). University degree in Biological Sciences/Nursing/Pharmacy is a minimum. Candidates must demonstrate: * strong oral and written communications skills and experience in medical scientific writing protocols and Clinical Trial Reports independently * experience and ability to recognize safety and efficacy data trends independently * knowledge of clinical trial design, statistics and pharmacokinetics * experienced with all aspects of the drug development process * knowledge of medical, scientific and clinical research techniques of the assigned areas * knowledge of GCP and local regulatory requirements
Novartis Oncology	na	MA	11/20/2009
Executive Assistant, Global Head Preclinical Safety
A minimum of 3-5 years as an administrative professional supporting executive level management. AS/BS degree required. Proven experience handling confidential and sensitive information is essential. Advanced knowledge of Microsoft Word, PowerPoint, Excel, Lotus Notes (or Outlook) required. Must possess excellent organization skills and have a high attention to detail with a desire to get the job completed accurately and in a timely manner.
Novartis Oncology	na	MA	11/20/2009
Executive Administrative Assistant, Ophthalmology
A minimum of seven years as an administrative professional supporting executive level management. AS/BS degree required. Proven experience handling confidential and sensitive information is essential. Advanced knowledge of Microsoft Word, PowerPoint, Excel, Lotus Notes (or Outlook) required. Must possess excellent organization skills and have a high attention to detail with a desire to get jobs completed accurately and in a timely manner. Project Management skills are a plus. Additionally, this candidate will be self-motivated, have excellent interpersonal skills and the ability to build professional relationships. They will also possess the ability to work independently and as an effective and engaged team member in a fast-paced environment. Strong initiative and follow through is essential. Candidates with a proven ability to provide guidance and/or support to Administrative Assistants is a preferred.
Novartis Oncology	na	NJ	11/20/2009
Director Translational Med Research Oncology
Education: ?MD/PharmD/PhD with revelant experience including previous scientific program leadership ?Must have significant, highly relevant experience in Oncology clinical trial & clinical operations. Experience: ?Conscientious, enthusiastic team player with excellent interpersonal as well as verbal and written skills. ?Strong leadership skills; ability to effectively work within internal teams across disciplines, with external collaborators and with contract research organizations. ?Must demonstrate good judgment and initiative. ?Must be hands-on, be detail oriented and work well under pressure. ?Demonstrated track records in the ability to effectively influence decisions inside the organization as well as the ability to drive efforts and overcome obstacles.
Novartis Oncology	na	NJ	11/20/2009
Dir Clinical Rsch Physician, Oncology
The successful candidate should have an MD and be Board Certified or board eligible in either hematology or oncology with several years (2 + years) of oncology/hematology clinical research experience in the industry. Essential requirement will be excellent presentation skills and strong background scientific knowledge base in Hematologic malignancies. Experience in both Clinical Development and/or Medical Affairs is preferable or a combination of experience in academic medicine with clinical research and/or 1 year of clinical development experience within the pharmaceutical industry. Experience leading the design, conduct, analysis and reporting of oncology clinical studies is desirable. Should have demonstrated significant successful interactions with oncology key opinion leaders/investigators. Candidates should have demonstrated the capability for strategic planning along with operational skill and experience related to clinical research involving both single and multiple centers. Ability to work across multiple functions is essential. Effective oral and written communication skills and strong leadership are sought.
Novartis Oncology	na	MA	11/20/2009
Diagnostics Early Stage Project Team Leader (Breast Cancer)
The candidate must possess a PhD in a relevant scientific field, such as Molecular Biology/Genetics, Cancer/Cell Biology, and Biochemistry, with at least 8 years of industrial experience, preferably in the areas of cancer diagnostics. * In-depth knowledge of disease mechanisms and the relevant signal transduction pathways at the molecular level is essential. * In-depth knowledge about various technologies for quantification of gene expression and protein detection as cancer diagnostic tools is important. * Knowledge of and experience in quality and regulatory requirements under which IVD molecular diagnostic products are developed, commercialized and supported (for example 510k or PMA applications, GLP, GCP, and GMP, etc.) are essential. * Strong management and leadership skills with proven ability to direct and lead project and cross-functional teams effectively in a dynamic environment are required. * Experience in leading and managing multi-disciplinary R&D projects for IVD applications is highly desirable. Experience in leading and/or managing diagnostic and/or prognostic product development for breast cancer is a plus. * Excellent communication and presentation skills are essential.
Novartis Oncology	na	CA	11/20/2009
Contract Mnfg Consultant (Emeryville, Calif)
Degree in related technical field (Biotechnology / Chemical Engineering / (Bio)chemistry) with doctorate (PhD) desirable or appropriate combination of education and experience. English fluent spoken and written; German & French spoken are a clear ?plus? Minimal 7-10 years confirmed experience in biotechnology manufacturing, ideally with direct responsibilities in manufacturing operations, 3rd-party management, toll-manufacturing activities or related area; Microbial expression system manufacturing background a plus.
Novartis Oncology	na	MA	11/20/2009
Computational Chemistry/Biology Research Investigator (Ph.D)
The ideal candidate will possess the following qualifications: ? Ph.D. degree in computational chemistry, computational biology or a related field, with 3+ years of related work experience. ? Familiarity with up-to-date biological screening paradigms. ? A proven track record in leveraging in silico techniques to drive basic science projects or in impacting hit finding activities in a drug discovery environment. ? A solid understanding of chemometrics, which includes QSAR methodologies, data mining and visualization, protein modeling, molecular docking, library design, conformational analysis, pharmacophore development, 2D and 3D similarity. ? A good understanding of bioinformatics and computational biology including gene expression data analysis and mining biological pathways to enhance target knowledge (GeneGO, Ingenuity). ? Demonstrate the ability to work independently as effectively as being able to collaborate in multidisciplinary teams. ? Strong analytical and problem-solving skills and scientific creativity are essential. ? Excellent oral and written communication skills and organizational skills are required. The following qualifications are a plus: ? A solid experience in a pharmaceutical or biotech environment. ? Background in medicinal chemistry and basic knowledge of synthetic organic chemistry. ? Programming skills in C/C++/C#, Java and scripting in Perl/Python and Pipeline Pilot.
Novartis Oncology	na	MA	11/20/2009
Computational ADME Scientist (BS/MS)
Candidates possessing an M.Sc. in Computational Chemistry or a closely related discipline with 5+ years of experience in in silico modeling in the drug metabolism and pharmacokinetics field within a pharmaceutical or biotechnology company. An in-depth understanding of all aspects of computational modeling within DMPK with special emphasis on descriptor calculation software, multivariate modeling approaches and application in the drug discovery setting is required. A successful candidate must be able to plan, conduct and interpret ADME modeling investigations in support of drug discovery efforts. A good working knowledge of drug metabolism and pharmacokinetics is required, with strong competencies in computational modeling via PLS, RF, neural networks or similar, as well as descriptor calculation software. Experience with pharmacokinetic modeling software (e.g. WinNonLin), programming language (e.g. C++, Java), and Linux operating systems is highly desired. A successful candidate will need excellent interpersonal skills, particularly oral and written communication skills.
Novartis Oncology	na	NJ	11/20/2009
Clinical Research Scientist/Sr. CRS
1. Minimum 2 years experience in drug development for CRS role. Clinical trial experience preferred. 2. Basic working knowledge of clinical database systems 3. Knowledge of clinical trial design; basic statistics and pharmacokinetics a plus. 4. Solid medical/scientific writing skills; ability to effectively communicate across the business organization 5. Knowledge of Oncology therapeutic area 6. Knowledge of good clinical practices (GCP/ICH) and regulatory requirements. 7. Ability to collaborate and work effectively in teams. 8. Demonstrates competencies in line with established profile. 9. Ability to manage multiple projects simultaneously. 10. Effectively manage project goals/objectives and timelines. 11.Collaborate with cross functional areas to support project deliverables. 12.Up to 20% travel
Novartis Oncology	na	MA	11/20/2009
BS/MS Research Associate: Molecular Pharmacology
A BS/MS life science degree with proven record of accomplishment and at least 3 years of prior drug discovery experience is required. The candidate must be well organized and able to work independently to plan, execute, interpret and troubleshoot experiments. Strong oral and written communication skills are essential. Excellent time management and multi-tasking skills are required, along with the ability to work collaboratively within a team environment.
Novartis Oncology	na	MA	11/20/2009
BS/MS Research Associate-Mass Spectrometry
Successful candidate will have minimally a BSc degree in the appropriate scientific area, with at least 2-3 years experience of extraction of low molecular weight analytes from plasma and/or tissues and developing LC and/or LC/MS methods to undertake their analysis. Experience with lipids measurement is preferred, but not essential.
Novartis Oncology	na	MA	11/20/2009
BS/MS Research Associate - Biochemistry Cellular Biology
BS/MS degree in cell biology, biochemistry, or molecular biology with 2+ years of relevant research experience is required. Experience in immunohistochemistry, immunoprecipitation, protein Western blot, protein interaction study, cell culture, and other cell biology/biochemical techniques. Demonstrated experience with executing experiments, interpreting results, and recording data while functioning independently. Effective oral and written communication skills. We are looking for a motivated candidate that works efficiently and collaboratively in a team environment.
Novartis Oncology	na	MA	11/20/2009
BS/MS Associate: In Vivo Pharmacology Oncology Translational Medicine
B.S./M.S. degree in Pharmacology, Molecular Biology, Biochemistry, or equivalent with 2-4 years of experience in animal models of human diseases, preferably in industrial oncology drug discovery. Practice in handling and dosing of rodents and formulation of test compounds is critical. A very strong background in molecular and cell biology with a good knowledge of statistics is essential. Familiarity with Excel, Word, Power Point and graphics applications, as well as excellent writing, communication, and inter-personal skills are very important. The ability to independently prepare drafts of publication-style reports will be a plus.
Novartis Oncology	na	CA	11/20/2009
Biopharmaceutical Mfg Microbial Fermentation Expert - Vacaville, CA
-PhD in Microbiology, Biochemistry, Biochemical/Chemical Engineering -English required; German or French desirable -Minimum of 5 years in a commercial manufacturing environment
Novartis Oncology	na	MA	11/20/2009
Bioinformatics, BMD Expert
Minimum requirements The successful candidate will have a Ph.D. in bioinformatics, engineering, physics, statistics, applied mathematics, or a related field with a strong computational background. The candidate should have experience (2+ years) analyzing genome-scale data sets and a working knowledge of molecular biology. Fluency in at least one statistical package (R/Bioconductor preferred) and one programming or scripting language (e.g. Perl, Ruby, Java, Python) is a must, as is experience in a Unix/Linux environment. Familiarity with software packages such as Partek, GeneSpring, GeneData Analyst, and Matlab is also required. Experience with relational databases and SQL is a plus. The successful candidate will be a team player with good communications skills, capable of discussing complex computational concepts with scientists from a variety of backgrounds. Required years of experience One - Three Years Education Doctorate Degree
Novartis Oncology	na	MA	11/20/2009
Bioinformatics - Oncology Translational Science
The ideal candidate will have an MS or higher in computational biology or a related field, with a minimum of 3-5 years research experience. A strong understanding of the application of statistics to biological problems, and experience in the analysis of genomic data, are required. Strong communication skills and a proven track record of interacting with scientific teams are also required. The candidate should be a strong scientific programmer, and ideally will be proficient in Perl and the R statistical language.
Novartis Oncology	na	MA	11/20/2009
Asc Director Biostatistics
Education (minimum/desirable): PhD or Masters Degree (or equivalent degree) in Statistics, Data mining, Bioinformatics or related field with 3 years or 5 years of experience respectively for senior role. Languages: Fluent English (oral and written). Experience/Professional requirement: ? Proven knowledge and expertise in statistics, data mining and/or bioinformatics and their applications to clinical trials. Experience with a wide range of advanced statistical methods. Strong analytical capabilities and data exploration skills. ? Experience in main tasks of a program statistician and as a team leader. ? Proven knowledge of drug development. ? Background knowledge and strong interest in life sciences. ? Proven knowledge of general statistical software packages (e.g. SAS, R/Splus/MATLAB). Knowledge of specialized statistical/data mining tools. ? Good communication, presentation and consultancy skills. ? Creative mind with good problem solving skills.
Novartis Oncology	na	NJ	11/20/2009
Asc Dir/ Dir New Product Strategies
A combination of science/marketing-business degrees; advanced degrees preferred; Minimum of 8 years of Pharma industry experience is required that include sales, medical science liaison and/or product management. At least 4 years of oncology experience and knowledge of US market. The candidate must possess strong interpersonal, communication and analytical/strategic thinking abilities. 25% travel is a requirement of this position.
Novartis Oncology	na	CA	11/20/2009
Asc Dir Quality Assurance-CMO (Emeryville, Calif)
-Bachelor or higher in Biochemistry, Chemistry, Microbiology or another related science -Fluent in speaking / writing in English -10 or more years experience in the pharmaceutical industry, with direct experience with Biopharmaceutical APIs. Experience in QA Operations, production, QC and/or other relevant operational areas, but must include minimally 5 years in QA, and 3 years of management and or project management experience.
Novartis Oncology	na	CO	11/20/2009
Analytical Research Scientist
BS Degree and 3-7 years experience. Masters Degree and 3 - 4 years experience. PhD - 1 to 3 years experience. Previous method development experience required. Knowledge of cGMPs. Pharmaceutical industry experience preferred.
Biogen Idec, Inc.	Cambridge	MA	11/20/2009
Principal Scientist, Bioanalytical Chem
PhD in a science major such as Chemistry and Biochemistry · >8 years experience in pharmaceutical industry or contract research organization · Experience in managing/conducting high throughput LC/MS/MS bioanalytical studies to support discovery small molecule projects. · Excellent organizational, interpersonal and communication skills. · Solid experience in people and performance management. · Demonstrated record of scientific publications.
Biogen Idec, Inc.	Cambridge	MA	11/20/2009
Scientist II, Bioanalytical
A Ph.D. in cell biology/molecular biology/immunology with 5-7 years of industry experience in a related field is required. Experience in immunoassay development, cell based assay development using a variety of technologies such as ELISA, Biacore, flow cytometry, reporter gene assays, statistical analysis of data is required. Familiarity with PK/PD concepts, and experience in supporting pre-clinical and clinical studies, interaction with pharmacokinetics scientists, toxicologists, clinicians and with regulatory authorities is desirable. Familiarity with GLP compliance procedures and guidelines is a must.
Biogen Idec, Inc.	Waltham	MA	11/20/2009
Clinical Trial Manager
â?¢Typically requires at least 5+ years of global drug development with experience managing clinical projects within time, budget, and quality expectations. â?¢Experience in hematology/oncology clinical research and development very desirable, especially in the areas of hemophilia and clotting disorders. â?¢NDA/BLA or MAA experience desirable, particularly within an orphan/rare disease therapeutic area. â?¢Thorough knowledge of GCP, ICH guidelines and awareness of global regulatory requirements/differences for clinical development. â?¢Detail and process oriented, with excellent project management skills, including risk assessment and contingency planning. â?¢Demonstrated leadership, communication, and organizational skills, along with problem solving, conflict resolution, and team building skills. â?¢Proven excellence in cross-functional matrix and/or cross-cultural partnership setting preferred.
Biogen Idec, Inc.	Raleigh/Durham	NC	11/20/2009
Scientist I, Stability
Minimum of 3 years direct experience in stability / formulation of biological and/or small molecule products in the Pharmaceutical industry, with 6+ years industry experience. PhD with 6+ years industry experience preferred, or BS/MS degree in Biology, Chemistry, Biochemistry, Chemical/Biochemical Engineering, or related disciplines with equivalent experience.
Biogen Idec, Inc.	Waltham	MA	11/20/2009
Scientist II
â?¢3-5 years of industry experience in (peptide/protein) analytical chemistry in a research/product development setting. â?¢Understanding and hands-on experience with a wide range of analytical chemistry techniques: HPLC (reversed-phase, size-exclusion, ion exchange), Electrophoresis (SDS-PAGE/IEF/CE), Protein Sequencing, Peptide Mapping, Carbohydrate Analysis and Mass Spectrometry. â?¢Knowledge and experience with amino acid post-translational modifications. â?¢Understanding and hands-on experience with biophysical techniques: ITC and Light Scattering â?¢Excellent oral, written and interpersonal communication skills and an ability to work across scientific disciplines. â?¢Experience with FDA/ICH guidelines. â?¢Knowledge of statistics and the ability to interpret experimental data to summarize the key findings. â?¢Meticulous attention to detail in following procedures, preparing written documentation and execution of experiments. â?¢Perform complex assays and investigate/troubleshoot assay problems.
Biogen Idec, Inc.	San Diego	CA	11/20/2009
Scientist II, BioPharm Develop
A Ph.D. in Biochemistry/Chemistry/Pharmaceutics/Chemical Engineering or a related discipline with a minimum of two years biopharmaceutical industry experience or relevant postdoctoral experience is required. The candidate should have excellent laboratory, computer, documentation, communication and organizational skills. Experience with protein formulation and analysis is required.
Biogen Idec, Inc.	Cambridge	MA	11/20/2009
Manager, EHS â?? R&D Support, Radiation Safety Office
The successful candidate will also have experience in one or more of the following: -Biosafety program - Providing oversight for the implementation and documentation of a biosafety program -Material Safety Data Sheet program - Providing oversight to product MSDS development process -Potent compound program â?? Supporting the implementation of an active pharmaceutical ingredient exposure control program. -Green Chemistry â?? Developing and implementing green chemistry principles in an R&D setting. Qualifications Successful candidate will have demonstrated the following experience: 8-10 years working in a biotechnology or pharmaceutical environment with a good understanding of scientific principles and practices. Experience as a safety professional applying a working knowledge of regulatory requirements and dealing with relevant federal, state and local regulatory agencies. Masters degree and Certified Health Physicist certification preferred.
Biogen Idec, Inc.	Waltham	MA	11/20/2009
Clinical Program Leader
â?¢Typically requires at least 8+ years of global drug development with experience managing clinical projects within time, budget, and quality expectations. â?¢Experience in hemophelia, thrombosis and/or oncology clinical research and development is very desirable â?¢NDA/BLA or MAA experience desirable, particularly within an orphan/rare disease therapeutic area. â?¢Thorough knowledge of GCP, ICH guidelines and awareness of global regulatory requirements/differences for clinical development. â?¢Detail and process oriented, with excellent project management skills, including risk assessment and contingency planning. â?¢Demonstrated leadership, communication, and organizational skills, along with problem solving, conflict resolution, and team building skills. â?¢Proven excellence in cross-functional matrix and/or cross-cultural partnership setting preferred.
Biogen Idec, Inc.	Cambridge	MA	11/20/2009
Scientist II, BioPharm Develop
â?¢Experience in solid state chemistry and material science technology. â?¢Expertise in pre-formulation (characterization of physiochemical properties). â?¢Experience in drug discovery support and solubilizing techniques to support medicinal chemistry, pharmacology, DMPK and PCDS. â?¢Expertise in polymorphism, salt screening/salt selection
Biogen Idec, Inc.	Cambridge	MA	11/20/2009
Principal Scientist, Pathologist
â?¢5 years of experience in toxicologic pathology is desirable. â?¢Excellent written and spoken communication skills are expected. â?¢Experience and proven ability to work with scientists and professionals from a wide variety of disciplines in a dynamic, project-driven environment â?¢Desire to have impact on the development of novel pharmaceuticals
Biogen Idec, Inc.	Waltham	MA	11/20/2009
Associate Scientist
A minimum of 3+ years of industrial research experience. The successful candidate should be responsible, motivated, flexible, a good team-player, have excellent oral and written communication skills, be able to collaborate with cross-functional teams.
Biogen Idec, Inc.	Cambridge	MA	11/20/2009
Director, Small Molecule Product Quality Management
Ph.D. in Chemistry, Pharmaceutical Sciences or equivalent with 10+ years of experience in Analytical Development, Process Chemistry or Manufacturing, including 3+ years in Quality or Regulatory departments of Pharmaceutical Company/ies. Experience in working with external collaborations for manufacturing, CMC projects and matrix managed projects is desirable. The candidate should possess working knowledge of Quality Assurance, Quality Control, cGMP compliance and regulatory requirements for multiple regulated territories. Success factors for this leadership position are ability develop people, change management, ability to drive teamwork for timely decisions in a multi-disciplinary, matrix managed results oriented environment.
Biogen Idec, Inc.	Cambridge	MA	11/20/2009
Scientist II, Stability
Minimum of 3 years direct experience in stability / formulation of biological and/or small molecule products in the Pharmaceutical industry, with 10+ years industry experience. PhD with 10+ years industry experience preferred, or BS/MS degree in Biology, Chemistry, Biochemistry, Chemical/Biochemical Engineering, or related disciplines with equivalent experience.
Teva Pharmaceuticals USA	North Wales	PA	11/20/2009
Business/Market Research Analyst
Teva Pharmaceuticals USA	Horsham	PA	11/20/2009
Employment Law Counsel
Teva Pharmaceuticals USA	Horsham	PA	11/20/2009
Sr Director, Clinical Reg Affairs- Women's Health
Teva Pharmaceuticals USA	North Wales	PA	11/20/2009
Sr. Manager, Network Administration & IT Security
Teva Pharmaceuticals USA	North Wales	PA	11/20/2009
Talent Development Specialist
Agilent Technologies, Inc. US	Anaheim	CA	11/20/2009
LCMS Product Specialist-Los Angeles
? Strategic Selling Skills (Executive Selling, Solution Selling)3-5 years ? High degree of LCMS application and platform domain competency ? Strategic Selling Skills (Executive Selling, Solution Selling)3-5 years ? LCMS Industry and Market Knowledge ? Excellent Verbal and Written Communication Skills as well as Interpersonal and Presentation Skills ? Teaming/Collaboration Skills (resource mgmt. and team leadership) ? B.S., M.S. or PhD in Biology, Chemistry, or Molecular Biology ~cb~09/09/09
Agilent Technologies, Inc. US	Wilmington	DE	11/20/2009
Online Sales Specialist - Intern
Completion of sophomore/junior/senior year towards a BA/BS in Chemistry, Biochemistry, or related science degree Would also consider Business, Marketing or similar discipline Proficiency in the use of Microsoft Office - Excel, Word, Outlook Strong interest in interacting directly with customers (via phone, email) Excellent verbal, written and phone communications skills Must be a team player with ability to work in a fast paced, dynamic team environment
Agilent Technologies, Inc. US	Santa Clara	CA	11/20/2009
Applications Engineer
Requires: - BS in biology, biochemistry, molecular biology; related discipline or equivalent. Master or PhD preferred. - 3+ years experience with life science software products - Experience with systems biology software products - Experience in interacting with customers in a pre-sales and/or post sales support role - Experience in generating and presenting technical training materials - Experience in interacting with cross-functional groups including sales, marketing and R&D Geo Location: Santa Clara, California cb~09/11/09
Agilent Technologies, Inc. US	Santa Clara	CA	11/20/2009
LC/MS Proteomics Scientist
PhD Degree or equivalent in Chemistry, BioChemistry, Biology, or related field. Minimum of 4 years relevant experience. The successful person for this position will: ? Be comfortable with all aspects of LC/MS analysis of proteins: sample preparation, instrument operation, data analysis, and data interpretation and processing ? Have the ability to use mathematical, theoretical modeling and software tools to develop predictive models for improving methods and data mining algorithms ? Have an understanding of the use of statistics in data interpretation and experimental design ? Be well-versed in the scientific method ? Have an understanding of mass spectrometry instrumentation, ion optics, and sources ? Have familiarity with and the ability to write software tools to assist in data mining ? Have a good understanding of proteomics in relation to other aspects of systems biology ? Be an effective communicator and team player ~cb~11/12/09
Agilent Technologies, Inc. US	Santa Clara	CA	11/20/2009
Nucleic Acid Chemist - Genomics R&D
Qualifications : ? Ph.D. degree in Organic Chemistry, Biochemistry or equivalent ? 4+ years relevant experience in industry and/or academia ? Strong theoretical knowledge and hands-on applications of modern Nucleic Acid chemistries required ? Strong knowledge and experience developing DNA and RNA synthesis processes is highly desired ? Knowledge of Chemical and Physical property Analytical techniques is highly desired, including LC/MS, NMR, viscosimetry, tensiometry, etc. ? Knowledge of Surface chemistry and surface analytical techniques a plus ? Proficiency in molecular biology techniques (electrophoresis, enzymatic assays, ?) and experimental troubleshooting a plus ? Proficiency with PCR & qPCR methodologies a plus ? Previous experience with microarrays and a working knowledge of statistical methods a plus ? Computer literacy and hands-on experience working with database software applications ? Excellent communications skills and time management skills ? Ability and enthusiasm to work in a collaborative team environment ~cb~11/12/09
Agilent Technologies, Inc. US	AnaheimEl SegundoFolsomGarden GroveLa JollaMenlo ParkPalo AltoPleasantonRedwood CityRohnert ParkRosevilleSan DiegoSan FranciscoSan JoseSanta BarbaraSanta ClaraSanta RosaWestlake Village	CA	11/20/2009
Product Marketing Engineer
? Bachelor of Science in biology, biochemistry, molecular biology, bioinformatics, or related discipline required. Master or PhD preferred. ? Understanding of software tools used in copy number and SNP studies ? Ability to communicate and discuss technical information on copy number and SNP analysis/bioinformatics, genetics, and genomic studies. ? Knowledge of key software platforms for genetic analysis and bioinformatics tools and databases such as the eArray, DGV, NCBI and UCSC Genome Browser. ? Exceptional cross-functional communication skills - proven ability to influence at all levels of the organization. ? Demonstrated use of marketing skills and market knowledge to define and commercialize products that result in business success. ? Experience in working with worldwide customers and is a strong advocate for customer focus and customer driven development. cb~10/01/09
Agilent Technologies, Inc. US	Boulder	CO	11/20/2009
API Process Development Scientist
Requires: - PhD Chemistry, Biochemistry; or Life Science discipline or equivalent - 3+ years hands on process development experience in pharmaceutical or biotechnology industrial - Pharmaceutical pilot palnt experience desired - Downstream and purification experience desirable - Hands on experience with HPLC, GC-MS, LC-MS, MS-MS, NMR and other supporting analytical technologies for chemical synthesis -Experience with DOE, statistical process control, Process Analytic Technology (PAT) applications and Quality by Design (QbD) initiatives desired - A proven track record in product/process development of API's that have been successfully transferred validated and approved by the FDA or corresponding regulatory authority. - Experience in development and successful transfer of safe, robust and scalable processes for the preparation of APIs. - Knowledge of ICH Q7 and cGMP guidelines highly desired - Excellent communication (oral and written), computer skills and interpersonal skills a must - Ability to interface with global cross-functional internal and external customers and partners - Track record of success in working with multiple projects in a fast pace environment managing to aggressive time lines and deliver projects on time - Available for occasional business travel Geo Location: Boulder, CO ~cb~10/20/09
Agilent Technologies, Inc. US	FolsomMenlo ParkPalo AltoPleasantonRedwood CityRohnert ParkRosevilleSan FranciscoSan JoseSanta ClaraSanta Rosa	CA	11/20/2009
Instrument Firmware Developer
Requires: BS degree in EE, CS or equivalent; MS is preferred - 5+ years of experience in an instrument firmware development role. Experience designing analytical equipment is strongly desired. - Strong skills in programming to include most of the following: o VxWorks o Linux and/or Unix o C, C++ o Assembler o DSP o Signal Processing o Programmable Logic Design (FPGA) o Network programming (TCP/IP, OSI layer model etc.) - Strong skills in interfacing with analog and digital electronics: o System architecture and design o Communications protocols o Driver development o Display and keyboard protocols - Other desired skills: o Experience in IC design o Experience in PCA/PCB design o Experience in Analytical Instruments - Good communication and documentation skills. - Works effectively in a multi-disciplined environment and with other functions (manufacturing, marketing, etc).
Agilent Technologies, Inc. US	Boulder	CO	11/20/2009
Quality Control Analyst
This is a solutions oriented environment where your energy, enthusiasm and pro-active approach will not only help drive Agilent's continued growth and development, but also your own career success. EDUCATION and/or EXPERIENCE Bachelor's degree (B.S.) or equivalent in chemistry or related life sciences field; and five to ten years related experience and/or training; or equivalent combination of education and experience. Five to ten years experience working in a GMP production environment is required. 1. Knowledge of GMP guidelines as well as international regulations pertaining to the production of APIs and drug products. 2. Knowledge and understanding of the oligonucleotide manufacturing or related pharmaceutical manufacturing processes. 3. Skill in communication, written and verbal; will be handling various relations issues and will be confronted with various interactions 4. Knowledge of and skill in using computer software and hardware applications, including Microsoft products and the Internet. 5. Skill in managing various projects; must be able to use individual discretion in completing work assignments; while assisting the group in establishing priorities, setting standards and working collectively to accomplish deadlines and objectives 6. Ability to read, analyze, and interpret industry related periodicals, SOPs, and government regulations. Ability to write reports, business correspondence, and procedures. Ability to respond to common inquiries or complaints from customers, co-workers, subordinates, and supervisors regarding the products and processes. Geo Location: Boulder CO cb~11/11/09
Agilent Technologies, Inc. US	Santa Clara	CA	11/20/2009
Regional Government Security Manager (West)
- MUST currently hold a SCI level security clearance with a current Single Scope Background Investigation (SSBI). - Must have a firm understanding of the security policies, procedures and directive of the DoD, National Industrial Security Program and Intelligence Community SCI security programs. - Bachelors Degree in Criminal Justice, Security Management, Industrial Security, Business Management or equivalent combination of education and experience. - 5 to 10 years of experience in the Government Security Field. - Knowledgeable in the use of JPAS, DIAS COMSEC and DoD/OPM Electronic Personnel Security Questionnaire software packages. - Proficiency with Microsoft Office products is essential. - Requires the ability to make sound decisions, manage time, take independent action, analyze problems and provide focused solutions. - Demonstrated ability to effectively communicate information to various audiences and all levels of the organization both verbally and through written communications. - Must be highly organized, be willing to work in a team environment, be able to prioritize tasking, perform in a multi-tasked and dynamic environment. - Must be dependable, responsive, customer focused and possess the qualities of diplomacy, tact, excellent judgment, discretion and initiative. ~cb~10/05/09
Agilent Technologies, Inc. US	Santa Clara	CA	11/20/2009
Product Marketing Engineer
? Bachelor of Science in biology, biochemistry, molecular biology, bioinformatics, or related discipline is required. Master or PhD preferred. ? Ability to communicate and discuss technical information on copy number and SNP analysis/bioinformatics, genetics, and genomic studies. ? Knowledge of key software platforms for genetic analysis and bioinformatics tools and databases such as the eArray, DGV, NCBI and UCSC Genome Browser. ? Exceptional cross-functional communication skills - proven ability to influence at all levels of the organization. ? Demonstrated use of marketing skills and market knowledge to define and commercialize products that result in business success. ? Experience in working with worldwide customers and is a strong advocate for customer focus and customer driven development.
Agilent Technologies, Inc. US	Santa Clara	CA	11/20/2009
Applications Scientist - Microarrays & QPCR
Key Areas of Expertise: Must have expertise in the following key areas: -Microarrays ? Agilent arrays: Gene Expression, ChIP-on Chip, CGH -QPCR ? both probe and SYBR Green assay experience desired -Agilent Bioanalyzer -Use of bioinformatics software, such as GeneSpring or ArrayAssist to analyze microarray data Education/Experience: ?Must have a B.S. or M.S. in Biology, Molecular Biology, or Biochemistry. A PhD is preferred. ?5 years lab experience with microarrays and QPCR ?Lab experience with Stratagene and Agilent products is a plus ?Must be a team player ?Excellent verbal and written communication, organizational, and project management skills -Ability to interface with global multidiscipline internal/external cross function teams -Ability to demonstrate excellent outbound phone calling communication skills. -Ability to solve a broad range of problems of varying scope and complexity. -Proactively acts to understand customer needs and identify solutions to non-standard tasks/queries; actively creates business opportunities. Geo Location: May reside in the Santa Clara, CA - La Jolla, CA - or Wilmington De Office No relocation assistance available. cb~10/08/09
Agilent Technologies, Inc. US	Santa Clara	CA	11/20/2009
Human Resources Business Partner
? BS/MS Degree in Business/ HR/OD or equivalent ? 8 years business experience in progressively challenging responsibilities in the following areas: leadership development of senior business team, organizational development/effectiveness, consulting, change management and talent management. ? A minimum of 3-5 years of HR experience within the Life Sciences space. ? Experience supporting Life Sciences channels preferred. ? A working knowledge of general HR practices a must along with the ability to influence HR strategy and policy using previous knowledge and experience from other business and work environments. ? The successful candidate will be an experienced business and human resources professional who has had experience within a heavily matrixed organization. This candidate will have related industry experience in the life science/biotech industry, with an emphasis in strategic planning, the ability to facilitate and relate to people across cultures and levels, and proven leadership skills. Geo Location: San Francisco/Bay Area
Agilent Technologies, Inc. US	MiamiTampa	FL	11/20/2009
Academic Sales Account Manager-Florida
Requires - BS/MS in a Life Science discipline (advanced degree preferred) and - 3+ years direct sales experience with a demonstrated track record of success - High level of expertise in Liquid Chromatography including a working knowledge of Fast LC (UHPLC)and LCMS. - Proteomics/biochemistry product expertise within varied industries and customer types. - Strong business development and sales/closing skills. - Must have excellent communication (written and verbal) and teamwork skills. - Able to interface comfortably at high levels within the customer management structure Geographic Location: Tampa/Miami
Agilent Technologies, Inc. US	Newport	DE	11/20/2009
Chemical Process Engineer
Qualifications Minimum of 4 years experience in chemical process manufacturing Bachelors or Masters Degree in chemical engineering or chemistry Demonstrated ability to apply chemical process fundamentals Extensive cross-functional team experience with demonstrated excellent teamwork skills Demonstrated success with process transfer and scale-up from R&D Previous manufacturing experience in an ISO9000 environment Demonstrated success improving process performance with respect to quality, rate, and yield Proven ability to find successful solutions to multiple problems of varying scope and complexity Demonstrated ability to work across multiple functions leading and managing projects Excellent written and oral communication skills Desired Qualifications: 5 to 8 years of experience Experience with batch chemical processing Experiences applying LEAN principles in a manufacturing environment Experience with colloidal science - experience with colloidal silica a plus Experience working within a Six Sigma organization with Green Belt or Black Belt certification ~cb~10/28/09
Agilent Technologies, Inc. US	Houston	TX	11/20/2009
Service Sales Specialist ? Southern US Region
Requires - BS/MS in Scientific, Engineering or Business discipline or equivalent. - 3+ years hands on laboratory or industry experience with instrumentation hardware, software, applications coupled with industry regulatory requirements such as (GLP, GMP, FDA) highly desired - 3+ years sales experience with a demonstrated track record of success in projects or sales at major accounts highly desired. - Ability to translate the Value Proposition of service as a financial and operational benefit to meet customer needs. - Strong business development, sales negotiating, and sales closing skills. - Must have excellent communication skills (written and verbal) and teamwork skills. - Outstanding presentation, planning and organizational skills - High level knowledge of instrument support services business - Computer literate with advanced skills using Microsoft suite of products (Outlook, Excel, Word, Powerpoint, Access) plus other IT systems. - Able to interface comfortably at high levels within the customer management structure - Demonstrated attention to detail and ability to manage large volumes of data. - Must be available for up to 60% business travel - Live in Houston, or surrounding communities Region Includes: Texas, Oklahoma, Louisiana ~cb~11/09/09
Agilent Technologies, Inc. US	Wilmington	DE	11/20/2009
Marketing Program Manager
? Undergraduate degree in Marketing or Business Administration. Strongly prefer chemistry or Biological Sciences degree. ? Minimum of 7 years of demonstrated results in a marketing role or relevant experience ? Worldwide experience developing outbound marketing programs to drive demand for new and existing products, as well as encourage repeat purchasing ? Well developed strategic thinking skills, project management skills, experience working with outside suppliers, a proven track record of measuring and enhancing program effectiveness, strong initiative, and the ability to work with a diverse group of individuals are critical. ? Demonstrated experience developing justifications for marketing investments (ROI analysis) ? Demonstrated results orientation, including developing fact-driven, business goal-focused plans that align with strategic objectives ? Effective project management and organizational skills ? Clear and compelling writing skills; strong oral communication skills; strong content presentation skills ? Ability to work collaboratively with a diverse group of individuals cross-organizationally, cross-functionally and within a global matrix ? Strong initiative and creativity ? Experience in relationship marketing, retention, and loyalty strategies using a range of direct marketing channels ? Proven ability to understand the needs and buying influences of a scientific target audience
Agilent Technologies, Inc. US	Santa Rosa	CA	11/20/2009
Semiconductor Fab Integration Engineer
M.S. or Ph.D. in Electrical Engineering, Physics, Materials Science, Mechanical Engineering, Chemical Engineering or equivalent experience. Experience with advanced semiconductor and/or MEMS processes and devices is essential and specific skills in III-V device physics and processing are highly desirable. Experience with statistical process control and design of experiments is desired. Candidates should have excellent interpersonal, problem solving, and communication skills for successful inter-group and intra-group interactions. US Citizenship/Permanent Resident status is recommended, but applications from highly qualified candidates requiring work sponsorship will also be considered. Candidates requiring work sponsorship must be eligible for access to export controlled electronics technology. Geo Location: Santa Rosa, CA ~cb~11/02/09
Agilent Technologies, Inc. US	Santa Clara	CA	11/20/2009
HPLC Bio-Separations Application Chemist
? Advanced Degree in Biochemistry, Molecular and Cellular Biology, or equivalent (demonstrated by 5+ years working experience in analytical HPLC bio-separations and confirmation of technical HPLC and Bio-Chromatography knowledge) ? Demonstrated expertise in operating HPLC systems and using a variety HPLC Bio-Columns including ion exchange, size exclusion, reverse phase, hydrophobic interaction and affinity ? Demonstrated experience in operating LC/MS and/or capillary electrophoresis systems for Biologic analysis preferred but not required ? Proven track record of self motivation and initiative ? Excellent verbal and written communication skills ? Ability to travel world wide as required up to 30% of the time ? Biopharmaceutical or Biotechnology expertise is critical to this position ~cb~11/01/09
Agilent Technologies, Inc. US	Santa Clara	CA	11/20/2009
Applications Engineer
Requires: - BS in biology, biochemistry, molecular biology; related discipline or equivalent. Master or PhD preferred. - 3+ years experience with life science software products - Experience with systems biology software products - Experience in interacting with customers in a pre-sales and/or post sales support role - Experience in generating and presenting technical training materials - Experience in interacting with cross-functional groups including sales, marketing and R&D Geo Location: Santa Clara, California
Agilent Technologies, Inc. US	Westlake Village	CA	11/20/2009
Field Service Engineer- Westlake Village
Description : As the Field Technical Support Representative for a high tech growth business serving the Chemical Analysis and Life Science markets, your primary responsibilities will include: Installation, repair and qualification services for Agilent and non-Agilent analytical instruments (LC/GC/MS) products for customers, on-site. Provides service in accordance to a maintenance contract, which may involve a managed service arrangement. Will be part of a team that delivers services on-site for large volume customers. Perform the duties of a Customer Service Representative for the Life Sciences and Chemical Analysis Group (LSCA) of Agilent Technologies. Responsibilities include on-site installation, customer training, repair and troubleshooting of hardware, and provide routine preventative maintenance, qualifications, and verification services. Typical products include Liquid Chromatographs, Gas Chromatographs, Mass Spectrometers, UV/VIS Spectrophotometers and Data Systems. Job focus will be on customer satisfaction by providing customers with high quality services. Other responsibilities include adherence to environmental health and safety guidelines, managing parts, coordinating resources, training, organization, providing feedback to manufacturing divisions, working with sales forces, and maintaining up to date technical knowledge for assigned products. Agilent Technologies is the world's premier measurement company. Agilent provides core electronic and bio-analytical measurement tools to engineers, service providers, researchers and scientists in the electronics, communications, life science research, environmental and petrochemical industries. ~cb~11/05/09
Agilent Technologies, Inc. US	Garden Grove	CA	11/20/2009
Scientist I
MS/Ph.D. or equivalent industrial experience required Strong protein chemistry background essential: - conjugation - purification Experience working with immunoglobulins desired Diagnostics industry experience desired ~cb~11/11/09
Agilent Technologies, Inc. US	Columbia	MD	11/20/2009
Federal Inside Account Manager
? The successful candidate needs to have at a minimum a BS Degree in the science such as Chemistry, Biology, Biochemistry or Physics. ? The ability to identify legislative funding to key agencies is necessary. Collaborating with Agilent's Government Affairs Office is required to facilitate earmark funding opportunities. ? Computer web searching and conducting federal business research and familiarity with the federal government's E-Buy and FedBizOpps and miscellaneous electronic interfaces is a requirement. ? They should have a strong understanding and can demonstrate computer skills and utilize programs to include Microsoft Office Suite 2007, Visio, Adobe etc. ? Excellent organization, written and verbal communication skills are required. Exception telephone communication skills are required and should be able to be demonstrated. ? The ability to research, formulate , format and organize electronic information to include sales data, government agency budget information, regulatory guidance affecting the federal programs, should be demonstrated and is required. ? Excellent probing and questioning skills required. ? A fundamental understanding of the sales process from prospecting and cold calling through closing deals is desired. ? The ability to use Customer Relationship Management software is desired. Previous experience with SAP-CRM is desired. ? The ability to accurately predict and forecast business close dates is desired. ? The ability to negotiate and mitigate critical customer issues is desired. ? The ability to configure and quote Agilent systems for sale is desired.
Agilent Technologies, Inc. US	Cedar Creek	TX	11/20/2009
Manufacturing Associate-Intermediate
This position requires a BS/BA degree in biological science or related field and one (1) to two (2) years of previous experience in chemistry, molecular biology and/or biochemistry. A strong working knowledge of standard laboratory techniques of molecular biology is required ( PCR, DNA and RNA isolation, bacterial transformations). Strong oral and written communication, organization, team building and computer skills essential. cb~11/11/2009
Agilent Technologies, Inc. US	Westlake Village	CA	11/20/2009
Field Service Engineer- Westlake Village
Description : Representative for the Life Sciences and Chemical Analysis Group (LSCA) of Agilent Technologies. Responsibilities include on-site installation, customer training, repair and troubleshooting of hardware, and provide routine preventative maintenance, qualifications, and verification services. Typical products include Liquid Chromatographs, Gas Chromatographs, Mass Spectrometers, UV/VIS Spectrophotometers and Data Systems. Job focus will be on customer satisfaction by providing customers with high quality services. Other responsibilities include adherence to environmental health and safety guidelines, managing parts, coordinating resources, training, organization, providing feedback to manufacturing divisions, working with sales forces, and maintaining up to date technical knowledge for assigned products. Will be part of a team that delivers on-site services at a major account. Agilent Technologies is the world's premier measurement company. Agilent provides core electronic and bio-analytical measurement tools to engineers, service providers, researchers and scientists in the electronics, communications, life science research, environmental and petrochemical industries. ~cb~11/17/09
BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Accounting Manager
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BD (Becton, Dickinson and Company)	San Diego	CA	11/20/2009
Biochemist I
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BD (Becton, Dickinson and Company)	Baltimore	MD	11/20/2009
Clinical Project Lead
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BD (Becton, Dickinson and Company)	Baltimore	MD	11/20/2009
Core Team Leader
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Director of Campaigns
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BD (Becton, Dickinson and Company)	Durham	NC	11/20/2009
Immunoassay Development Manager
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Instrument Assembly Associate I
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BD (Becton, Dickinson and Company)	Broken Bow	NE	11/20/2009
Intern - Quality Engineer/Microbiology
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Manager International Regulatory Affairs
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BD (Becton, Dickinson and Company)	Burlington	NC	11/20/2009
Manager Technical Product Support Cervical Programs
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Manager US Regulatory Affairs
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BD (Becton, Dickinson and Company)	San Diego	CA	11/20/2009
Manufacturing Manager - Tissue Culture
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
Metallurgist/Materials Engineer
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
Product Manager, Scientific Services
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Production Chemist I
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BD (Becton, Dickinson and Company)	San Diego	CA	11/20/2009
QA Inspector I
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Quality Engineer II
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Quality Engineer II
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
R&D Director, Additive and Chemistry
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
R&D Director, Preanalytical Systems
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
R&D Manager, Emerging Markets
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BD (Becton, Dickinson and Company)	Sandy	UT	11/20/2009
R&D Manager, Infusion Systems
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
R&D Manager, Packaging Technology
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
R&D Manager, Technology Development
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Reagent Dev Associate III
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Reagent Dev Associate III
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BD (Becton, Dickinson and Company)	Baltimore	MD	11/20/2009
Regulatory Affairs Specialist
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
Regulatory Affairs Specialist
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Reliability Engineer II
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Research Associate
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BD (Becton, Dickinson and Company)	San Diego	CA	11/20/2009
Research Associate III
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BD (Becton, Dickinson and Company)	Durham	NC	11/20/2009
Scientific Affairs Liaison
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BD (Becton, Dickinson and Company)	Baltimore	MD	11/20/2009
Scientist
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Scientist I
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BD (Becton, Dickinson and Company)	San Diego	CA	11/20/2009
Scientist I
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BD (Becton, Dickinson and Company)	San Diego	CA	11/20/2009
Scientist I
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BD (Becton, Dickinson and Company)	San Diego	CA	11/20/2009
Scientist II - Molecular Biology
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BD (Becton, Dickinson and Company)	Durham	NC	11/20/2009
Senior Clinical Trial Manager
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BD (Becton, Dickinson and Company)	Durham	NC	11/20/2009
Senior Marketing Manager ? Multiplexed Assay Products
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BD (Becton, Dickinson and Company)	Baltimore	MD	11/20/2009
Senior Regulatory Affairs Specialist
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BD (Becton, Dickinson and Company)	Baltimore	MD	11/20/2009
Senior Scientist
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BD (Becton, Dickinson and Company)	Research Triangle Park	NC	11/20/2009
Software Engineer
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Software Project Engineer
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Software Project Engineer
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Sr Algorithm Scientist Developer
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Sr Reagent Dev Associate
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Sr Scientist
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
Staff Engineer - Environmental Sustainability
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
Strategic Innovation Leader
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BD (Becton, Dickinson and Company)	Baltimore	MD	11/20/2009
System Project Engineer
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Technical Applications Specialist
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Technical Writer IV
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
WW Controller Cell Analysis
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openQ	Charlottesville	VA	11/19/2009
Data Research Project Manager
Skills: • Very thorough understanding of life sciences industry • Understanding of, and comfort with, reading medical literature and performing information searches on medically-related topics • Excellent verbal and written communication skills • Strong analytical skills and technical understanding of data acquisition, data structuring and data quality control • Prior experience interfacing with customers about data-related projects • Strong team player and the proven ability to work independently Education: • PhD in life sciences field preferred or Master’s degree and preferably at least 5 years relevant experience in life sciences driven data company
Strategic Diagnostics Inc.	Newark	DE	11/19/2009
Scientist III
Qualifications: (Knowledge, Skills and Abilities: Education, Experience, Job Skills, Equipment Skills, and Certifications) 1. B.S/B.A. in Biology, molecular biology, Chemistry, biochemistry/ microbiology/ immunology/ medical technology field with 5+years. MS or PhD generally required for this level with 1-2 years of experience. 2. Strong knowledge of QSR, cGMP and ISO regulations and guideline 3. Fully knowledgeable of Instrumentation used in molecular biology. 4. Demonstrated skill in the areas of protein purification and analysis; such as IMAC, Gel filtration, western blot. 5. Demonstrated skill in the areas of DNA manipulation; such as PCR and gene construction, sub-cloning and sequence analysis. Supervisory Responsibilities: May manage a team of scientists and technicians performing, training, coaching and aid in quarterly and yearly performance reviews, conducts disciplinary discussions as appropriate. Abilities: 1. Thorough understanding of molecular biology and protein biochemistry. 2. Must be familiar with accepted industry practices and regulations 3. Maintain broad knowledge of current scientific theories and practices. 4. Able to multitask 5. Able to work independently and lead a team of scientists 6. Able to organize and prioritize tasks for his/her self and others 7. Able to resolve problems with others 8. Good verbal and written communication 9. Develops SOP’s 10. Documents coaching Work Environment / Other Requirements: Works in a variety of lab environments that could lead to exposure to heat, cold, dry air, chemicals, odors and humidity. Ability to lift 50 pounds required
Strategic Diagnostics Inc.	Newark	DE	11/20/2009
Senior Scientist-Process Engineer
Experience in lateral flow, immunoassay, bioluminescence and other bioassays is preferred. MS or PhD generally required for this level with 8-12 years of experience. Individual must demonstrated technical expertise in a related business or field. Must be familiar with accepted industry practices and regulations. Prefer experience in a Food Industry, or Biopharmaceutical/Pharmaceutical Manufacturing environment.
Morphotek®, Inc.	Exton	PA	11/20/2009
Scientist, Bioanalytical Development
Knowledge/Skills/Abilities Required • BS/MS with 5-7 yrs or PhD with 0-2 yrs relevant experience required. • In-depth knowledge and understanding of bioanalytical assays for protein macromolecules with strong scientific and technical skills in method development and validation. • A minimum of 5 years of hands-on experience in the development and/or validation of quantitative ligand binding and immunogenicity assays for biologics (e.g. antibodies, proteins or peptides). • Well versed in current regulatory guidance and industry practices for development and validation of bioanalytical methods for large molecule biologics. • Excellent verbal and written communication skills. • Experience in GLP and/or clinical regulatory compliance is desired. • Strong analytical skills, and a demonstrated ability to work both independently and in a team setting required.
Morphotek®, Inc.	Exton	PA	11/19/2009
Sr. Scientist - Pharmacology
Job Requirements and Qualifications Education: PhD with training in pathology, cell biology or related fields, expertise in oncology preferred but not required. Must have at least 5 years experience in biotech/pharmaceutical industry. Strong experimental skills in human disease model development, mammalian tissue culture, vector transduction and imaging-related technology. Oncology experience is preferred. Experience in IHC is a plus. A thorough understanding of molecular oncology and immunology. Demonstrated experience in in vivo human disease model and an excellent publication record. Supervisory experience preferred. Excellent organizational, time management, communication, and interpersonal skills. Strong oral and written skills, and experience maintaining a record of studies in the form of notebooks, technical reports, summaries, protocols, and quantitative analyses. Other Information Special Information (Travel required, physical requirements, on-call schedules, and etc.): Some travel may be required.
Miltenyi Biotec Inc.	Auburn	CA	11/20/2009
Technical Support Scientist
Ph.D. in Immunology, Molecular Biology or similar field with 1-3 years experience in life sciences environment; or equivalent combination of education and experience. Flow cytometry experience is a must. We offer a competitive salary and excellent benefits package. There is no relocation associated with this position. EOE/AA To apply, go to: https://home.eease.com/recruit/?id=370281
Southern Research Institute	Frederick	MD	11/20/2009
Scientific Project Leader for Emerging Pathogens
Seeking qualified candidate with a PhD in life sciences discipline, MD, or DVM with a minimum of eight years prior experience managing NIH grants, contracts or projects in the biotech or pharmaceutical industry environment. Must be proficient in project management methodologies, have demonstrated success in generating/developing funding streams through successful proposal submissions; an outstanding publication record and documented combination of education, experience, and training to qualify as a study director within specified programs. Must be able to lead execution of large complex projects involving multiple technical staff at varying levels of expertise. Must be able to respond quickly to new funding opportunities while, at the same time, provide support to existing projects. Prior successful experience in a Contract Research Organization is highly preferred. Qualified candidate must be able to positively interact and communicate with individuals across the organization at all levels and positively engage current and potential funding sponsors within the government and private sector. Candidate must be able to work in a team environment and be capable of supporting and participating in related ongoing project lead by others. Must be able to be able to collaborate with others to accomplish a common goal. Prior documented experience working in infectious disease research, particularly virology, immunology, biomarkers, and animal models (small animal or NHP models) of infectious diseases. Well known standing in the field of human pathogenic viruses preferred. Experience in respiratory viruses, antiviral therapeutics, or vaccine discovery and development preferred. Prior GLP experience preferred. Must be able to obtain clearance for select agents. This position will work in a BSL2 and BSL3 plus environment and therefore must be able to meet the medical and vaccination requirements. This position is responsible for obtaining funding for and ensuring the successful execution of projects awarded. This position, as the study director of awarded projects, is responsible for the overall technical conduct of the study; interpretation, analysis, documentation, and reporting of results; issuance of study protocols and amendments; adherence to study protocols and amendments; following GLP practices; meeting all contract deliverables; and maintaining a positive relationship with the client. This position also ensures the quality of the product or service delivered; manages project budget and risk factors; and uses project management methodologies to ensure that projects are managed effectively. We operate in a matrix environment. This position may or may not have direct reports. Regardless of direct reporting technical staff, this position is responsible for the supervision of any/all individuals supporting the project to ensure high quality outcomes. This position is responsible for providing performance feedback to individuals supporting projects through informal and formal performance management processes. This position coordinates necessary technical talent with other project leaders and supervisors to ensure project needs are met. This position trains and develops others as necessary, provides mentoring and coaching, and seeks input from others when necessary. Prior supervision/leadership experience helpful. This position will report to the Director of Infectious Disease Research or the Program Leader. Work Environment & Conditions: Individuals who will enter BSL-2/BSL-3 labs must: satisfactorily complete medical requirements; obtain applicable vaccinations; pass and maintain in depth security and background checks, including clearance to handle select agents; wear required PPE; and must have effective communication skills. All offers of employment (and continued employment) are subject to drug testing. Applications must be made online at http://www.southernresearch.org / for position sr-02194
Miltenyi Biotec Inc.			11/20/2009
Technical Sales Consultant
Ph.D., M.S. or B.S. degree from a four-year college or university and two to four years experience in the life sciences environment; or equivalent combination of education and experience. Immunology and/or Molecular Biology background is preferred, and Ph.D. is highly desirable. Other Requirements: Must possess a valid driver’s license, evidence of insurance / insurability and ability to receive appropriate clearance to access restricted government accounts. We offer a competitive salary, commission, car allowance, and excellent benefits package. There is no relocation associated with this position. EOE/AA To apply, go to: https://home.eease.com/recruit/?id=367955
Miltenyi Biotec Inc.	Auburn	CA	11/19/2009
Marketing Product Manager - Auburn, CA
Bachelor’s or graduate degree in the life sciences, or MBA preferred. Must have in-depth technical knowledge and 2 to 5 years of experience in science field related to product line marketing; or equivalent combination of education and experience. We offer a competitive salary and excellent benefits package. There is no relocation associated with this position. EOE/AA https://home.eease.com/recruit/?id=229953