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Job Title	City	State	Posted on
AstraZeneca Pharmaceuticals	Delaware	DE	11/19/2009
Mechanic II
? High school diploma ? 3 years of active, hands-on experience in the installation, maintenance, repair and troubleshooting of refrigeration and HVAC/R equipment in commercial, industrial, manufacturing or research facilities. ? Completion of two or more years of a state accredited Journeyman program in HVAC/Refrigeration or equivalent technical program. ? Demonstrated ability with analytical/troubleshooting skills in HVAC controls (DDC and pneumatic) and refrigeration equipment ? Possess a valid EPA 608 Universal Certificate ? Demonstrated ability to make sound decisions and deal effectively with internal customers independently. ? Demonstrated ability to successfully complete complex assignments from start to finish ? Demonstrated ability to work independently and using safe work practices. ? Strong teamwork, interpersonal, communication, and writing skills ? Basic computer skills. Preferred Background ? Completion of a state accredited Journeyman program or equivalent Associates degree in an HVAC engineering technology program ? 5+ years of active, hands-on experience in the HVAC/Refrigeration trade
AstraZeneca Pharmaceuticals	Delaware	DE	11/19/2009
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.
Johnson & Johnson Family of Companies	Somerville	NJ	11/19/2009
Senior Engineer
A BS degree required. A MS degree preferred. Minimum 5 years of related engineering (related to electro mechanical devices) experience required. Experience in a highly regulated environment is highly preferred. Knowledge of ISO and cGMP regulations is required. Previous experience with leading and conducting process validation activities required. Experience with electro-mechanical manufacturing processes preferred. Competent working knowledge of DX methodologies, statistical techniques required. Good communication and presentation skills required. A certification in Process Excellence (Green Belt or Black Belt) is preferred. Competent PC literacy including CAD applications preferred. Due to technical upgrades, this requisition is replacing requisition # 0903157. Any candidates who have already applied to requisition # 0903157 are already being considered, therefore, you do not need to apply.
Johnson & Johnson Family of Companies		CA	11/19/2009
Staff Process Engineer
A minimum of a Bachelor's degree and a minimum of 9 years of engineering related experience OR a Masters degree and a minimum of 7 years of engineering related experience OR a Ph.D. and a minimum of 4 years of engineering related experience is required. Complex understanding of polymer and engineering fundamentals is required. Experience in a highly regulated industry is required. Experience in the medical device or pharmaceutical industry is an asset. A clear mastery of statistical and experimental engineering techniques is required. Proficiency with Microsoft Office, specifically Excel is required. Experience with Microsoft Project is preferred. Experience with balloon catheter process and polymer bonding is preferred. Experience with Six Sigma/Process Excellence Tools, Training, and/or Certification is preferred. Experience managing complex projects is required. Excellent verbal and written communication skills are required. This candidate will have strong analytical/problem solving skills. Ability to work on cross functional teams is required. The ability to develop and lead teams, strong collaborative skills, and the ability to negotiate and influence are required. This position will require that you be based in Menlo Park, CA and travel 10% of the time internationally and domestically. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies		CA	11/19/2009
Principal Engineer
BS degree in relevant discipline and 14 + years of related engineering experience; MS in relevant discipline and 12 + years of related engineering experience; Ph.D. in relevant discipline and 9 + years of related engineering experience. Has significant complex level engineering experience. PE License is desirable. Four plus years experience in the medical device industry is required. Possess a mastery of theoretical and practical fundamentals and experimental engineering techniques. Ability to manage several projects. Excellent verbal communication skills and written skillsIf you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies		CA	11/19/2009
Sr Engineer - R&D
BS degree in relevant discipline and at least five years of related engineering experience is required; or MS degree in relevant discipline and at least three years of related engineering experience. Experience in the medical device industry would be a requirement. Must possess the basic understanding of engineering fundamentals. English communication skills, written and oral is required.Experience with executing design control deliverables is also required. Experience with Cardio Vascular Products will be required in this role.If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies		NJ	11/19/2009
Intern - Finance MBA Leadership Development Program Summer 2010
Graduate student pursuing a full time Master's Degree in Finance or Accounting or MBA Minimum of 3 years of business experience.Leadership capabilities demonstrated through extracurricular activities, employment, and/or internship experiences.Must have permanent work authorization in the U.S. without requiring sponsorship.
Johnson & Johnson Family of Companies		NJ	11/19/2009
R&D Co-Op- Fall 2010
Candidates must be working towards a B.S., M.S., or PhD degree in Chemical Engineering, Materials (Science) Engineering, Biological or Biomedical Engineering, Biology, Chemistry, Pharmaceutical Sciences, or other related concentration. Candidates must possess a 3.0 GPA or higher. Candidates must be authorized to work in the U.S. for any employer.
Johnson & Johnson Family of Companies	Glendora	CA	11/19/2009
TEST LAB SUPERVISOR
Education and/or Experience: a Bachelors Degree in Electrical/Mechanical Engineering or related field with a minimum of 5 years industry experience and 3 years medical device experience. It is also required to have System Engineering experience in multi-disciplinary products ( Software and Hardware). Knowledge and experience in development processes and in documentation writing is an asset in this role. Lead, design, develop, and implement test equipment and test specifications is required.Strong knowledge of one or more of the following standards such as ASTM, UL, IEC 60601-1, ISO 8536-4 and ISO 10555-1 & -5 is preferred.Knowledge of GMP and other regulatory requirement is also preferred for this position.OTHER SKILLS and ABILITIES:Test Lab Supervisor will be expected to have strong analytical reasoning with excellent communication skills.Test Lab Supervisor will have the knowledge, skill and ability to provide technical support to project teams.If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Somerville	NJ	11/19/2009
Staff Mechanical Engineer
A minimum of a Bachelor's degree in Mechanical Engineering, Design Engineering, Biomedical Engineering or a related discipline is required. An advanced degree is an asset. A minimum of 2+ years work experience in product design/development or manufacturing processes testing is required. Experience in design and development of medical devices is an asset. Experience in design of mechanical devices, systems and/or electro-mechanical products is an asset. Successful completion of products from concept to launch is an asset. CAD ability in Solidworks, Mechanical Desktop or equivalent design software is an asset. A general knowledge and understanding of QSR, DOE, QFD, DFMA, and FMEA is an asset. Must be able to apply and comprehend a broad range of engineering and scientific assignments as well as have demonstrated the ability to work independently and within a group. Will utilize the support of technicians also assigned to the project team. Computer literate in project planning and or data acquisition is desirable. Must be self-motivating and innovative and be able to work on multiple projects with different priorities. Extensive verbal and technical writing skills as well as proven analytical and problem solving skills. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Somerville	NJ	11/19/2009
Senior Engineer
A minimum of a Bachelor's degree in an Engineering discipline is required. An advanced degree is an asset. A minimum of 5 years of related engineering experience in an FDA regulated environment is required. Knowledge of ISO and cGMP regulations is required. Previous experience with conducting design verification and validation testing in support regulatory submissions required. Experience with competitive benchmarking, and process qualifications is required. Engineering prototype evaluation is an asset. Project management experience required. Strong communication, and influencing skills are required. A certification in Process Excellence (Green Belt or Black Belt) is an asset. This position may require up to 25% domestic and international travel. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Somerville	NJ	11/19/2009
Senior Quality Engineer
A minimum of a Bachelor's degree in Engineering, Life Science, Physical Science or a related field is required, with an Advanced degree is preferred. A minimum of 4+ years of Quality Engineering experience is required. Experience in the medical device, pharmaceutical or other highly regulated industry is required. New product development experience is required. Supplier quality engineering experience is a plus. Experience with the development of Electro-mechanical devices is an asset. Knowledge of IEC 60601-1 is preferred. Knowledge of ISO and/or cGMP regulations is required. Strong knowledge in Quality Systems Regulations (QSR) preferred. ASQ certifications (CQE, CQM, CRE or CQA) is preferred. Six Sigma Green Belt or Black Belt is desired. Knowledge in Statistics, Sampling Planning, Reliability, Computer System Validation and Process Validation is an asset. Candidate must be able to communicate effectively at all levels within Quality as well as cross functionally with departments such as R&D, Operations, Purchasing, Marketing and Medical Affairs. This position may require up to 20% travel. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	San Angelo	TX	11/19/2009
Controls/Computer Integrated Manufacturing Engineer
A minimum of a Bachelors degree in a Computer Science/Engineering, Electrical Engineering, or Computer Integrated Manufacturing discipline with at least two years of programming or design experience is required. Required skills include demonstrated ability to contribute in a team environment supporting 24x7 production operations and continuous improvement programs from a technical improvement standpoint. The ability to supervise personnel would be an asset. In addition, the ability to manage and report project budgets and schedules is a must. Fluency with process/operating specifications and engineering processes and practices is required. Fluency with GMPs, regulations, project management tools (MS Project) would be desired. Knowledge of spreadsheets, word processing and associated software is required. Knowledge of MS Access would be preferred. The candidate should posses a strong work ethic, be self-motivated and able to work with little supervision. Technical competences should include: Object oriented programming is required preferably in .Net framework (VB and/or C#) or VB6 Development environment. Visual Studio 2005/2008 would be preferred, Database experience in Oracle or MS SQL Server highly desired. HMI/ operator interface development - FIX32, IFIX, or RSView preferred. Web programming - ASP/ASP.net, HTML preferred. Basic knowledge with Windows 2000, XP, and/or Vista required. This position will be based in San Angelo, TX. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies		CA	11/19/2009
Staff Engineer- FEA Analyst
EDUCATION and/or EXPERIENCE: MS in Engineering Mechanics (or related engineering discipline) and three or more years of related engineering experience; or Ph.D. in Engineering Mechanics (or related engineering discipline). Experience with ABAQUS IMPLICIT and/or EXPLICIT software in an industrial setting is strongly preferred.. Experience with Statistical Analysis, Metal Plasticity and Metallurgical Principles is preferable. Experience with using LINUX or UNIX operating systems is strongly preferred. Experience with CAD software is also strongly preferred. Experience in the medical device industry would be an asset. Other skills and abilities include: A clear mastery of theoretical and mechanics principals is required for this position and experience with experimental engineering techniques is an asset. English communication skills, written and oral are required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Piscataway	NJ	11/19/2009
SAP Global Process Subject Matter Expert - Master Data Management
A minimum of a Bachelor's degree is required. A Master's degree is preferred. A minimum of 5 years of experience in manufacturing roles within Operations or Supply Chain is required. A minimum of 2 years of experience within a Master Data Management role is highly desirable. A working knowledge of SAP is required. Experience working in an FDA regulated environment with an emphasis on Validation & Compliance of systems and processes is preferred. Experience working remotely with business partners in a global environment is preferred. Process re-engineering experience is preferred. Experience working with multiple franchises and sectors in a highly matrixed environment is preferred. Experience with any of the following is preferred: Process Flow Diagrams, Business user requirements and Documentation. Professional Certification with CPIM, CSCP, Six Sigma Black or Green Belt is preferred. This position will require up to 20% of domestic travel. This position will be based in Piscataway, NJ If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies		CA	11/19/2009
Staff Quality Engineer - Irwindale, CA
A minimum of a Bachelor's degree in Engineering, Physical, Biological, or natural sciences, along with a minimum of 8+ years of quality, manufacturing, or research and development experience in a medical device or other regulated industry is required. An MBA, Master's, or advanced degree in an applicable field of study is an asset. An American Society for Quality (ASQ) certification is an asset. Experience or knowledge of Six Sigma, Lean Manufacturing, or Process Excellence tools is desirable. Must have the ability to use broad knowledge of regulatory, technical, and business requirements to conduct due diligence assessments. Project management experience or skills ensuring fulfillment of new product development requirements is required. Development and implementation of Quality standards applicable to the medical device or other highly regulated industry required. Knowledge of Quality and Operations systems and processes, including GMP, in a regulated industry is required. A knowledge of Quality Systems Regulations (QSR) requirements as they relate to medical devices is required. Auditing experience is an asset. Knowledge of Quality Engineering, design control, and verification and validation (V&V) tools and methodologies required. The ability to effectively communicate with internal and external personnel at all levels of the organization will be needed. Well-developed influencing and negotiation skills and the ability to effectively train and mentor a diverse array of employees at all levels of the organization will be needed. Business and financial acumen an asset. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! Due to technical upgrades, this requisition is replacing requisition # 0903032. Any candidates who have already applied to requisition # 0903032 are already being considered, therefore, you do not need to apply.
Johnson & Johnson Family of Companies	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	Taunton	MA	11/19/2009
Manager, Clinical Research
Minimum of a Bachelors degree in Science or related Health Field is required in this role with a Masters Degree in Science/related Health Field preferred. Also preferred is an, MBA. 10 years industry experience with 7 years experience in the Pharmaceutical or Medical Device industries is required. Strong leadership skills and the ability to develop successful strategies while fully understanding the complex environment of the assigned program. Experience in multiple functional areas strongly preferred (Clinical, Marketing, R&D, Sales)Significant project management experience with cross-functional, cross-company and international project teams. Clinical trial experience is strongly preferred and international trial experience is a plus.Strong ability to communicate clinical information (concepts and results) in oral and written communication to experts (e.g., KOL, FDA reviewers) and to product development team members (e.g., clinicians, marketing personnel, engineers)Understanding of the contribution of scientific and medical affairs goals to company business strategiesExperience drafting or reviewing technical documents (e.g., Clinical protocols/reports, design FMEAs, IOVVs). Appropriate knowledge of GMP, GCP and regulations required.Proven insight into the integration of science, regulatory, and business principles as it pertains to the successful development of multi-center clinical studies.Understanding of reimbursement landscape in the US and OUS is beneficial.Prior experience in strategic roles, along with excellent written and oral communication skills, and experience presenting to senior management also required.Ability to foster a strong collaborative team environmentDemonstrated ability to collaborate and work effectively in a fast-paced matrix environmentDemonstrated negotiation and conflict resolutions skills, including the ability to influence without clear reporting authorityStrong professional diplomacy Strong organizational skills (e.g., able to manage multiple institutions and/or projects). If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	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	South San Francisco	CA	11/19/2009
Director, Medical Writing - Janssen AI, LLC
A minimum of a Bachelor's degree in a science or communication discipline with a minimum of 10 years medical writing experience in the clinical or laboratory setting, OR an Advanced Degree with 7 years medical writing experience in a clinical or laboratory setting preferred. Excellent leadership and management experience. Good understanding of experimental methods, research design, and statistical analysis. Ability to analyze medical data and interpret its significance within a pharmaceutical setting. Ability to interpret, analyze, and present statistical data obtained in a clinical trial. Advanced scientific, technical reading, writing and editing skills. Excellent oral communication skills. Proficient computer and word processing skills. Use of templates and experience with document management systems. Up to 5% yearly travel may be required (International as well as Domestic). If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	South San Francisco	CA	11/19/2009
Head of Biometrics (Senior Director) - Janssen AI, LLC
A Ph.D. degree in Biostatistics or closely related field is required. A minimum of 15 years of pharmaceutical experience with at least 5 years of management level experience. International experience is strongly desired. Excellent verbal and written communication skills. Must have a working knowledge of filing regulatory documents and complex statistical methods that apply to all phases of clinical trials. Strong attention to detail and accuracy is a must. Ability to effectively present information to senior management, regulatory authorities, public groups, and other departments. Demonstrated ability to integrate planning efforts across departments to ensure organizational effectiveness. Ability to cultivate internal and external relationships based on trust and respect in anticipation of future working relationships. Demonstrated ability to proactively maximize relationships to enable successful collaboration. Demonstrated ability to facilitate a beneficial resolution of conflict. Ability to articulate a clear vision and help others understand their relationship between their roles, the roles of others and the overall goals of the organization; ability to articulate the reason behind organizational changes and demonstrate flexibility, energy and resilience throughout change efforts. Demonstrated ability to work cooperatively within and outside the organization to accomplish the best outcomes; ability to work in diverse teams to optimize decision-making. Demonstrated ability to provide coaching and feedback to foster professional development while also supporting business goals. 10-15% International and Domestic travel is required.
Johnson & Johnson Family of Companies	Raynham	MA	11/19/2009
Platform Director
A minimum of a BS/BA degree is required with an MBA or other advanced degree highly preferred. A minimum of 6 years of total business experience is required, with at least 2 of those years in the following areas: a combination of R&D and marketing experience, brand or strategy marketing, or new product development project management is required. Medical Device experience is highly preferred. Experience in developing and presenting business strategies is required. Must have the ability to influence without authority across multiple levels. This position requires someone to be both strategic and tactical. Experience with financial modeling is preferred. Must possess demonstrated analytical skills. Must have experience with Voice of the Customer (VOC) and/or Job Outcomes Constraints (JOC) techniques and the ability to translate them. Must be able to utilize both written and oral communication skills to produce effective marketing materials. Must have experience making effective presentations to small and large groups at all levels. Must have experience working in cross functional teams, and be able to engage and get buy in from key internal stakeholders and drive teams towards consensus on product needs/opportunities. This position requires approximately 30% travel primarily domestic with some international travel. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Raynham	MA	11/19/2009
Staff Engineer/ Black Belt Process Driver
BS- Engineering, is required for this role and a Master's Degree in Engineering would be a plus. A strong technical background is also required.Black Belt certification in Design Excellence mandatory. A Master Black Belt is an asset in this role.2 years as certified Black Belt leading and delivering significant new product development projectsMedical device experience a significant plus. Experience in a regulated industry is required.Ability to align board members, cross-functional directors/managers and engineers to drive organizational change through effective leadership, interpersonal and communication skillsKnowledge of New Product Development, taking a product from concept through commercialization is a requirement.Ability to teach design excellence tools is required and the ability to help others complete Black and Green belt training is an asset.Ability to prioritize and complete multiple projects on time and within assigned resource constraints. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	Raleigh	NC	11/19/2009
Senior Quality Assurance Engineer
A minimum of a Bachelor's degree in Engineering, Science, Technology or a related discipline is required, with a minimum of 5+ years experience in a highly regulated industry required, with experience in the medical device or pharmaceutical industry preferred. A minimum of 3+ years experience as a Quality Engineer is required. CQE or equivalent certification is an asset. Experience with Chemical Processing, Chemistry, or in a related lab area is an asset. Thorough understanding of FDA Quality System Regulation, MDD, ISO 13485:2003, quality engineering methodology, and quality management principles are an asset. Working knowledge of Standards applicable to Medical Device Industry are an asset. Experience with medical device product design and manufacturing processes is an asset. Knowledge of statistical tools and techniques is an asset. Experience in analytical problem solving is an asset. Proven accomplishment in Quality System Auditing is an asset. FDA Notified Body experience as a team member is an asset. Personal computer and software applications experience, including e-mail, Internet applications, Word processing, spreadsheet, and database work is required. Statistical Analysis program, Minitab, or other statistics software experience is required. Must be able to work within a team and handle multiple tasks. Experience with dimensional tools (e.g. rulers, optical comparators, calipers, micrometers, pin gauges) and balances/scales is an asset. This position is located in Raleigh, NC. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today!
Johnson & Johnson Family of Companies	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	South San Francisco	CA	11/19/2009
Clinical Program Manager - Janssen AI, LLC
BS or BA in a relevant scientific discipline is required. Must possess at least 5 years of relevant clinical experience in the pharmaceutical (or similar) industry. Excellent interpersonal skills and demonstrated ability to lead is required. Experience in managing staff as well as mentoring and developing junior staff is preferred. Strong communication and influence skills and the ability to create a clear sense of direction is necessary. Must be able to resolve problems using national and international regulations and guidelines. Must have a demonstrated ability to successfully develop, implement, manage and complete clinical trials. Thorough knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is required. Experience in developing RFPs and selection and management of CROs/vendors is required. The ability to write study protocols, study reports, sections for investigator brochures and regulatory documents (e.g. IND, DNA, etc.) with little supervision is required. The ability to examine functional issues from a broader organizational perspective is required. The ability to participate in and/or lead departmental or interdepartmental strategic initiatives under limited supervision is required. Functional expertise to initiate, author, and/or contribute to SOP development, implementation and/or training is preferred. 25% travel is required, both international and domestic.
Johnson & Johnson Family of Companies	South San Francisco	CA	11/19/2009
Manager, Clinical Data Management - Janssen AI, LLC (1 of 2)
High School diploma required. Med Tech background preferred. BS/BA degree preferred. A background in Life Sciences is a plus. A minimum of 5+ years of data management experience within a pharmaceutical and/or health care environment required. Electronic data capture experience preferred. Experience managing external vendors is required. Knowledge of FDA regulatory requirements is strongly preferred.
Johnson & Johnson Family of Companies	South San Francisco	CA	11/19/2009
Senior Clinical Budget Analyst - Janssen AI, LLC
A Bachelor's Degree is required. Working knowledge of the clinical development process and 2+ years of experience in clinical budget development and management are required. Must possess an understanding of clinical trials, regulatory affairs, quality assurance, clinical trial materials, budgeting and routine contracts. Previous experience with industry benchmarking database(s) is strongly preferred. Excellent communication skills (both oral and written) are required. The ability to work effectively in cross-functional teams is required. Strong and proven negotiation and problem resolution skills are also required. Strong business acumen and an innovative spirit are required. Strong inter-personal and collaboration skills are required. Must possess the ability to accomplish substantial tasks with minimal supervision. Experience in assisting and drafting of legal contracts and familiarity of clinical budget development and negotiation is required.
Johnson & Johnson Family of Companies	South San Francisco	CA	11/19/2009
Senior Clinical Contract Analyst - Janssen AI, LLC
A Bachelor's Degree is required. A certificate of completion of formal course in Paralegal studies is preferred. Certification of Notary Public is a plus. Working knowledge of the clinical development process and 2+ years of experience in clinical budget development and management are required. Must possess an understanding of clinical trials, regulatory affairs, quality assurance, clinical trial materials, budgeting and routine contracts. Excellent communication skills (both oral and written) are required. The ability to work effectively in cross-functional teams is required. Strong business acumen and an innovative spirit are required. Strong inter-personal and collaboration skills are required. Must possess the ability to accomplish substantial tasks with minimal supervision. Familiarity of clinical budget development and/or negotiation is required.
Johnson & Johnson Family of Companies	South San Francisco	CA	11/19/2009
Global Commercial Leader - Janssen AI, LLC
Bachelor's degree required; advanced degree preferred. A minimum of 14 years of progressive marketing experience preferably in the pharmaceutical or devices industry; extensive line marketing experience (prefer strong US experience in an infusion/biological setting), senior brand responsibility, product launch experience, and team leadership required. Ideally will have demonstrated success in establishing new markets/new paradigms. A minimum of 2 years strategic global marketing leadership experience required. Demonstrated track record leading highly matrixed, cross-functional work teams composed of high-level managers and executives. Experience with global R&D programs preferred. Extensive experience accomplishing objectives through people. Position requires significant domestic and some international travel.
Johnson & Johnson Family of Companies	South San Francisco	CA	11/19/2009
Global Marketing Director, Infrastructure - Janssen AI, LLC
BA/BS required; Advanced degree in business or life sciences preferred. A minimum of 10 years of progressive marketing experience is required with a proven track record of exceptional team & cross-functional leadership. Pharmaceutical industry experience is highly preferred, significant line marketing experience with senior brand responsibility, is required. Global marketing experience and launch experience is preferred. Demonstrated global mindset with the ability to assimilate complex science quickly is required. This position requires up to 25% domestic/international travel.
Millennium Pharmaceuticals	Cambridge	MA	11/19/2009
Assoc Director - Solid Formulations
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
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
Senior Engineer
Minimum of a Bachelor's Degree or equivalent in Computer Science, Information Systems, Engineering, or related technical discipline (required) 8+ years of experience in security engineering Integration of AD and LDAP directory stores for authentication (AD) and directory attributes for administration roles, event management, and reporting Windows, linux, unix, networking technologies experience Lotus Notes experience a plus Certifications a plus Must possess good communication and mentoring skills Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline. Vertex Pharmaceuticals
Vertex Pharmaceuticals	Cambridge	MA	11/19/2009
Senior Scientist, Process Safety
- Ph.D. or BS/MS in Chemical Engineering or Chemistry - 6 + years of relevant work experience in API or fine chemical process development, scale-up, troubleshooting, and optimization - A strong and sound understanding of synthetic organic chemistry and chemical engineering fundamentals along with common chemical hazards/incompatibilities with a familiarity with modern in-situ process analysis tools (FTIR, n-IR, UV-Vis) being a plus - Experience with the application of common safety evaluation instrumentation such as TGA, DSC, RC-1, ARC, RSST and the resulting data in the identification and mitigation of chemical process hazards - Demonstrated experience with modeling complex, physicochemical systems and statistical design of experiments as well as a fluency with common physical property and process modeling tools (Aspen, Dynochem, Matlab, etc.) - Knowledge of applied kinetics, thermodynamics, and transport fundamentals - A nature driven by high productivity and producing results - The ablity to generate and implement original ideas and solutions that contribute materially to the success and development of drug substance candidates - Excellent communication and interpersonal skills, strong organization and planning skills, a high level of technical aptitude and creativity, and the ability to interact, lead, and collaborate within an interdisciplinary team environment comprised of organic, physical, and analytical chemists; project team members; and manufacturing personnel Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company?s strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex?s product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection. Vertex Pharmaceuticals
Vertex Pharmaceuticals	Cambridge	MA	11/19/2009
Associate Director, Market Research
- A Bachelor's degree in a quantitative discipline such as finance, engineering, mathematics or statistics with a preference for an advanced degree in business, economics, mathematics, or statistics - 7 years experience in pharmaceutical and/or biotechnology market research, with a majority of this experience being company or client side - Experience with managed markets market research including working knowledge of key primary and secondary data sources as well as selection of pricing research vendors and pricing research execution - Ability to multitask as well as be productive, and innovative, in a dynamic, fast paced environment while working both independently and coaching others on aspects of market research projects - Strong interpersonal skills along with the proven ability to succeed in matrix team environment. Previous team management experience would be a plus - Outstanding written and verbal communication skills with the established ability to effectively communicate study results to diverse audiences - Strong computer skills including advanced competency with PowerPoint. Working knowledge of SPSS or SAS preferred Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company?s strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex?s product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection. Vertex Pharmaceuticals
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
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
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
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.	Elkton	VA	11/19/2009
Staff Chemical Engineer
This position requires candidate to be currently enrolled in a MS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002019. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Senior Chemical Engineer
This position requires candidate to be currently enrolled in a PhD program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002024.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Chemical Engineer
This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001998. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Chemical Engineer
This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001988. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Chemical Engineer
This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001978. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Manufacturing Technical Rotation
This position requires candidate to be currently enrolled in a PhD program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002053.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003868. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003878. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003888. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003898. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003908. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Merck Manufacturing Business Intern
This position requires applicant to be currently working toward a Bachelors degree in Supply Chain Management, Engineering, Business or a related discipline. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ADM003948. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003918. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Merck Manufacturing Engineering Intern
This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003928. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Merck Manufacturing Graduate Intern
This position requires applicant to be currently working toward a working toward graduate degree in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Statistics or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000318. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Chemical Engineer
Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002008. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Quality Compliance Auditor
Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating day shift (6AM-6PM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001961. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Quality Compliance Specialist
Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 3 years of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends, and to complete several months of training on first shift. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001974. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Quality Compliance Auditor
Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends, and to complete several months of training on first shift. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Principal Development Engineer
Education:BS, MS or PhD Degree in Chemical Engineering, Materials Engineering/Science or Pharmaceutics with a minimum of 8 years post-bachelors degree experience in Technical Operations, Process Development, or related experience (Ph.D., 4 years or more experience required). Required:At least 3 years of experience in the formulation/development and technology transfer of controlled release dosage forms. Strong Chemical Engineering skills with a desire to perform hands-on work including design and execution of experiments at both pilot scale and during scale up. Thorough understanding of polymer chemistry and other materials along with their impact on drug release. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ENG002042. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Staff Engineer
Education:· B.S in Engineering, Biological Sciences, Chemistry or Physics. M.S. in Engineering, Biological Sciences, Chemistry or Physics preferred.Required:· Minimum of 4 years work experience required; with 2 years of work experience specifically in the field of validation. Specific experience in at least one of the following areas is required:· Filter performance qualification using Filter Integrity testers, bubble point, and diffusive flow testing. Experience in validation desired; alternatively, experience in engineering or operations is acceptable with use of sterilizing filters, tangential flow filtration, ultra filtration, and vent filters.· Container/ Closure Integrity testing using microbial ingress and helium leak testing. Experience in validation desired; alternatively, experience in engineering or operations using welders, sealers, and aseptic fluid transfers using sterile bags and manifolds is acceptable.· Experience in a GMP or ISO13485 laboratory performing microbiology, environmental monitoring or engineering development work. Support the GVTE / BSV Lab Coordinator, with performing instrument qualification, metrology, SOP development , creating training material, lab notebook review, performance of internal audits (chemical hygiene, safety, 5S, GMP), and carrying out improvements activities and corrective actions in response to audits.Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ENG002123. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Staff Scientist
Education Minimum Requirement: Bachelors Degree in microbiology, biochemistry, biochemical engineering or related field plus three years related experience. Masters Degree D in microbiology, biochemistry, biochemical engineering or related field preferred. Required Experience and Skills - Strong technical background in cell culture, molecular and microbiology, excellent communication skills, demonstrated ability to troubleshoot bioprocesses, and the ability to work in a team environment. The candidate must be experienced in aseptic technique, be able to work efficiently in a high paced environment and collaborate well with others. Desired Experience and Skills - Virology experience and Assay development. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ENG002118. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Principal Development Engineer
Education:BS, MS or PhD Degree in Chemical Engineering or Materials Engineering/Science. Required:A minimum of 8 years post-bachelors degree experience in Manufacturing, Process Development, or acceptable related experience (Ph.D., 4 years or more experience required). Strong Chemical Engineering skills with a desire to perform hands-on work including design and execution of experiments at various scales (lab/ pilot plant etc). Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE001837. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Sr. Engineer - Sterile Process/Capital Project Support
Requirements:Bachelor of Science in Chemical Engineering, Mechanical Engineering, or Biomedical Engineering5 years experience in a process engineering support or capital project engineering role supporting an FDA regulated processPreferred:Experience with a sterile/aseptic processExperience with a pharmaceutical manufacturing process Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #CHE002167. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Release Coordinator
EducationA Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. RequiredAt least three (3) years of relevant post-degree work experience in a manufacturing or research environment or a related field. Strong analytical, problem solving, oral and written communication skills, leadership, and attention to detail. Solid understanding of regulatory requirements and GMPs. PreferredAseptic gowning may be required. Tites may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000134. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Release Associate
Required:B.S. degree with a technical emphasis in an appropriate scientific or engineering field. At least one year of relevant post-degree work experience in a laboratory, manufacturing, or quality position. Evidence of leadership skills coupled with good oral and written communication skills, i.e. effective presentation of concepts and ideas, as well as interpersonal and conflict resolution skills. Attention to detail, flexibility and an awareness of production and attendant quality control problems. Preferred:Familiarity with manufacturing batch records is a key skill necessary for success in this position; prior batch record experience is a strong plus. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000124. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Sr. Engineer/Scientist - Manufacturing Process Technical Support
Minimum Qualifications: Bachelor's degree in Chemical, BioChemical or Bioprocess Engineering with 5 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR Master's degree in Chemical, BioChemical or Bioprocess Engineering with 2 years experience in a GMP Biopharmaceutical manufacturing or research and development environment Preferred Qualifications:Experience providing technical support of a GMP manufacturing process, specifically in protein purification and/or fermentation. Experience writing technical documentation: such as change controls, protocols, operating procedures. Experience with commissioning, qualification, and validation of biopharmaceutical equipment and processes. Demonstrated expertise in bioprocessing unit operations such as fermentation, chromatography, tangential flow filtration Demonstrated ability to lead a group of individuals in task oriented assignments such as technical investigations, root cause analysis, equipment installation Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002082. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Elkton	VA	11/19/2009
Process Engineer/Scientist - Pharmaceutical Manufacturing Process Support
Basic Qualifications: Bachelor's degree in Chemical, BioChemical or Bioprocess Engineering with 7 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR Master's degree in Chemical, BioChemical or Bioprocess Engineering with 5 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR PhD in Chemical, BioChemical or Bioprocess Engineering Preferred Qualifications:Experience leading and developing people and teams Experience and expertise in protein purification or fermentation Project management experience Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002084. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Quality Compliance Auditor
Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating day shift (6AM-6PM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000131. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Quality Compliance Auditor
Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating day shift (6AM-6PM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000137. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Quality Compliance Auditor
Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000141. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Quality Compliance Auditor
Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000133. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Rahway	NJ	11/19/2009
Project Scientist
Education:BS in Biological Sciences Required. MS in Biological Sciences Preferred Required experience: 3 years post-bachelors degree experience in supply for therapeutic proteins/vaccines/biologics (may be combination of post-graduate education and/or work-related experience.) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #PRO007555. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	Rahway	NJ	11/19/2009
Staff Biochemist
Education:BS in Biological Sciences Required. Required experience: 1 to 3 years post-bachelors degree experience in analysis and supply of biologics (may be combination of post-graduate education and/or work-related experience.) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #PRO007589. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Lead, Learning & Behavior Realization
Educational Requirements: Minimum of five years in a highly regulated industry (preferably pharmaceutical). BS/BA degree in education, science or engineering. Required experience and skills:Minimum of four years experience in instructional design/technology, organizational development, or performance consulting. Excellent communication skills Ability to facilitate cross-functional teams. Ability to collaborate with others. Self-motivated and adaptable Ability to plan and organize work. Ability to learn, understand and communicate business needs and solutions. Ability to solve problems creatively. Computer Skills Ability to drive results. Ability to think strategically. Ability to influence stakeholders. Ability to leverage diversity. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #EMP000210 . Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck
Merck & Co., Inc.	West Point	PA	11/19/2009
Quality Engineer
Education:Bachelor's degree required. The desired educational background is a BS in an appropriate Engineering field, Operations Improvement, or Business Administration. Other fields of study will be considered if accompanied by significant relevant experience. Required:Three or more years of related Industrial, Production, or Staff experience, obtained through post-degree work in one or more of the following areas: Project management, operations support, or process improvement Financial analysis, resource allocation, or budget / profit plan management Capital plans and/or projects Regulatory and/or compendial requirements Preferred:Experience in one or more of the following areas: Facilities / space planning Operations research techniques Vendor relations and/or contract negotiation Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA002013. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means
Merck & Co., Inc.	West Point	PA	11/19/2009
Release Analyst
EducationA Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. RequiredAt least three (3) years of relevant post-degree work experience in a manufacturing or research environment or a related field. Strong analytical, problem solving, oral and written communication skills, leadership, and attention to detail. Solid understanding of regulatory requirements and GMPs. PreferredAseptic gowning may be required. Tites may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000149. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	RTP	Durham	11/19/2009
Operational Coach- Manufacturing Maintenance Leader
Required:Minimum of 6 years experience in a manufacturing maintenance role within a GMP facility. Minimum 4 years coaching/supervisory experience Bachelor degree in Engineering or Science Asset:Vaccine/sterile experience Plant maintenance, project engineering and/or operations experience Computer Maintenance Management System (Maximo) SAP Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000272. Merck is an equal opportunity employer, M/F/D/V proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.
Merck & Co., Inc.	West Point	PA	11/19/2009
Process Engineer
Education: BS in Chemical Engineering, Bio-Engineering or Biosciences. MS in Chemical Engineering, Bio-Engineering, or Biosciences preferred. Required:Demonstrated Technical Strength. Strong Analytical Problem-Solving. Ability to lead teams. Effective Communication, both verbal and written. Strong Collaboration & Leadership experience. Preferred:GMP experience, Cell Culture and/or Virology experience. Previous Technology Transfer experience. Experience with Aseptic Processing and related equipment desired. Knowledge and experience of CIP and SIP. Knowledge or experience of six sigma methodology, process analytical technology, process monitoring and control. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # PRO007596. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm Representatives Please Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by
Novartis Oncology	na	MA	11/20/2009
Sr Director Regulatory Affairs
Advanced education degree in life-sciences, engineering or public health or law. 1. Greater than 10 years work related profession experience. 2. 7 years experience in drug/diagnostic regulatory affairs. 3. Knowledge of drug development and regulation affairs requirements 4. Familiar with regulatory issues and challenges associated with Drug/Diagnostic co-development and companion diagnostic. 5. Have a track record in successful data submission for FDA and EMEA approval 6. Sound knowledge of international customs and business practice 7. Profound understanding of molecular technologies and the impact on outcomes and diagnostic results 8. Leadership capabilities working across cultures, expertise and backgrounds 9. Excellent negotiation skills with regulatory staff on various levels of hierarchy 10. Outstanding interpersonal and communication skills for bridging scientific and business participants, for negotiating timelines and for effective international collaboration. 11. Outstanding verbal and written communications
Novartis Oncology	na	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
Scientist I, Mammalian Cell Line Development
A B.S. or M.S. degree in biology, cell biology, immunology, or related life science field and 3 plus years of experience in biotechnology or pharmaceutical industry are required. Recent Ph.D. graduates will also be considered. The Scientist must be able to work independently to design experiments and perform therapeutic protein expression and production runs to accomplish team goals. Candidate should bring a highly collaborative spirit with an ability to work on multiple projects and maintain well organized records and notebooks. The successful candidate should also have excellent written and oral communication skills, and be able to thrive in our fast-paced and dynamic organization.
Novartis Oncology	na	MA	11/20/2009
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	NC	11/20/2009
Process Validation Engineer III
EDUCATION/EXPERIENCE: BS and 4 years of related experience in Pharmaceutical or related industry or MS and 2 years of related experience in Pharmaceutical or related industry or PhD and no significant experience
Novartis Oncology	na	NJ	11/20/2009
Postdoctoral Fellow, DMPK
Ph.D. degree with 0-3 years of post-PhD research experience in pharmacokinetics, biopharmaceutics, biomedical engineering, chemical engineering, or other related discipline with specific experience in PK/PD and/or PK modeling is required. The candidate must be able to work independently and have a strong understanding of PK/PD. The candidate should should be able to provide technical assistance on individual projects, spanning across multiple therapeutic areas. Hands-on experience in PK and PK/PD modeling is a must. Good oral and written communication skills are required. Previous experience with some of the PKPD softwares such as: WinNonlin; ADAPT; NONMEM, GastroPlus.
Novartis Oncology	na	CA	11/20/2009
Mfg Process Engineer - Vacaville, Calif
BS in Chemical, Biochemical, or Mechanical Engineering, preference in Chemical/Biochemical Engineering. Written and spoken English Up to 5 years in a commercial manufacturing environment
Novartis Oncology	na	NE	11/20/2009
Lean Sensei
Required:: ? Bachelor?s degree in science- or engineering-related field. MS or MBA preferred. ? 15+ years of business/operations management or manufacturing experience with management responsibilities. ? Lean expert training, excellent skills using IT applications to organize and analyze data (MS-Access, MS-Excel, Minitab, IGraphX, etc.). Desired: Proficiency in design for manufacturability. ? Hands-on experience with deploying TPS-based lean methods in operations is a critical requirement. ? Technical mastery of continuous improvement tools and methodologies. ? Certified Lean Expert/TPS based. ? Results-oriented, strong analytical skills, and demonstrated process improvement success in managing large teams in a continuous improvement culture. ? Proven change agent and ability to lead teams through: Making case for change; stakeholder management; change communications; removing barriers; setting milestones and acknowledging progress; and reinforcing change through organizational systems. ? Strategic focus. ? Collaborative Leadership: Willingness to work on the shop floor and lead by example; ability to influence decision making with or without authority; facilitate groups with diverse perspectives; and bring teams to agreement. High tolerance for ambiguity. ? Must have strong interpersonal and communication skills that build productive relationships and influences others, both within the business and across organizations. ? Must have a strong track record of collaborating effectively with others in the spirit of common objectives. ? Communication: Ability to interact with all levels of the business (senior leaders to working teams); exceptionally good listening skills; able to present complex or new ideas with clarity and simplicity. ? Planning and Execution: Excellent project management and prioritization skills. Solid business acumen. Able to deliver results despite shifting environment. ? Analytical Problem Solving: Able to identify problems; apply structured and disciplined methodology to identify root cause using data. Innovative and effective solution development, risk mitigation and execution. Hands-on experience with most of the following Lean/problem-solving tools: DMAIC, Lean, voice of the customer, SMART problem and goal statements, SIPOC and process mapping, process capability analysis, failure mode and effects analysis, graphical methods, measurement systems analysis, hypothesis testing, analytical hierarchy process, benchmarking, design of experiments, quality function deployment, control charts, standardized work.
Novartis Oncology	na	MA	11/20/2009
Lab Head, Mammalian Cell Line Development
A Ph.D. and postdoctoral fellowship in biology, cell biology, immunology, or related life science field and experience in the biotechnology or pharmaceutical industry are required. Managerial experience is also desirable. The Lab Head is expected to perform and supervise hands-on laboratory work. A highly collaborative spirit and ability to work on multiple projects is desirable. Successful candidate will have excellent written and oral communication skills, will be well organized and will thrive in a fast-paced, lean and dynamic organization.
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
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	NJ	11/20/2009
Executive Director, Quality Assurance
minimum required travel 60%required. Education and training: Graduate in Chemistry, Pharmacy, Microbiology or another related science Excellent oral and written English communication skills. Second language is preferred. Minimum 10 years board experience in Pharmaceutical industry or a related regulatory industry. Valid operational experience includes production of QA/QC operations, quality management experience, development or other relevant experience working at a regulatory health authority. Broad business awareness. Expertise in one or more areas: Facilities, CSV, Laboratory, Aseptic manufacturing, Microbiology, Biopharmaceuticals, Pharmacovigilance, etc. Expertise in Compliance and health authority interactions. Expertise in GxPs, working knowledge of legal, quality engineering concepts, risk management techniques. Experience working on teams (multiple roles) and projects. Working knowledge of global regulatory requirements required. Involvement in Industry forums desired.
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
Biogen Idec, Inc.	Cambridge	MA	11/20/2009
Director, Discovery & Preclinical IT
ā?¢ In-depth knowledge of informatics and IT solutions in the discovery and preclinical space. ā?¢ Proven expertise in global solutions design, development, and production implementation. ā?¢ Excellent managerial and operational skills, combined with strong customer focus. ā?¢ Ability to effectively communicate with peers, upper management, and business partners ā?¢ Demonstrated ability to articulate and ā??sellā? a vision for IT-enabled drug discovery. ā?¢ Proven ability to lead multi-disciplinary, cross-cultural project teams. ā?¢ Comfortable working in a matrix organization and managing by influence. ā?¢ Previous managerial experience in a similar industrial position preferred. ā?¢ Demonstrated ability to forge academic and commercial collaborations is a strong plus.
Teva Pharmaceuticals USA	North Wales	PA	11/20/2009
Sr. Manager, Network Administration & IT Security
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	Columbia	MD	11/20/2009
System Architect
Qualifications: Qualifications: ? Bachelors or Master Degree or University Degree in Electrical/Electronic or Computer Engineering and 5+ years applicable experience in architecting and implementing complex software solutions, and a deep understanding of Mobile Communication Systems and Networks. (Including Cell Phone and other Mobile Communications Infrastructure). ? Software project management, definition, development and deployment expertise. ? Understanding of the customers data streams and architecture where our products content will be used. ? Direct experience with SIGINT customers, products and applications. ? Experience in SIGINT acquisition systems, familiarity with content acquisition platforms in wireline, cellular telecom, and IP. ? End USER expertise in SIGINT missions ? Experience with end user, installation and commissioning of new systems within customer environments is highly desired. ? Familiarity with 7 layer OSI model and current and evolving telecoms standards including Wireless Protocols, with a strong background in IP ? Self starter and ability to self-learn ? Strong interpersonal/relationship skills, solid written and verbal communications ? US citizenship required. ? Current US Government Security Clearance -or- ability to process for and obtain US Government Security Clearance
Agilent Technologies, Inc. US	Colorado Springs	CO	11/20/2009
R&D Software Engineer
Position requires: ? BS/MS Degree in Computer Science or equivalent and a minimum of 5+ years SW development experience ? 5+ yrs Java Development ? Experience building devkits is preferred ? C++ experience desirable ? Linux OS experience desirable ? Telecom or general networking industry knowledge is helpful ( as related to network quality of service) ? Experience with WEB application development ? Knowledge of FLEX GUI Builder, REST API, and XML/XSD, GUI human factors background is an added plus ? Excellent verbal and written communication skills ? Ability to work with cross-functional global teams ? Results-oriented and track record of success in delivering to critical project deadlines ? Strong sense of initiative and ability to work autonomously These additional skills are strongly preferred: ? Experience with Object and data modeling ? Web based transactions (managing sessions, persistence of the data, JPA) ~cb~8/27/2009
Agilent Technologies, Inc. US	Colorado Springs	CO	11/20/2009
R&D Software Engineer
Position requires: ? BS/MS Degree in Computer Science or equivalent and a minimum of 5+ years SW development experience ? 5+ yrs Java Development ? Linux OS experience ? Telecom or general networking industry knowledge is helpful ( as related to network quality of service) ? Experience with WEB application development ? Knowledge of FLEX GUI Builder, REST API, and XML/XSD, GUI human factors background is an added plus ? Excellent verbal and written communication skills ? Ability to work with cross-functional global teams ? Results-oriented and track record of success in delivering to critical project deadlines ? Strong sense of initiative and ability to work autonomously These additional skills are strongly preferred: ? Experience with Object and data modeling ? Web based transactions (managing sessions, persistence of the data, JPA)
Agilent Technologies, Inc. US	Colorado Springs	CO	11/20/2009
R&D Network Engineer
This role requires a well rounded, hands-on Network Engineer who will function as a Network expert, Software development engineer, and Test Engineer. The individual must possess a BS Engineering ( or equivalent) and possess advanced knowledge in a high-performance datacenter with direct support and network services engineering responsibilities. Network certifications are strongly preferred. C++ and XML Software development skills are also strongly preferred. Other key skills: ? Advanced experience with configuration and support of Cisco routers and switches (minimum 7+ years) 1.Desired Cisco hardware knowledge with platforms 6500, 7500, 4500, 3800, 3700, 2900 ? Advanced experience with configuration and support of Hewlett Packard switches (minimum 5+ years) 1.Desired Hewlett Packard knowledge with platforms Procurve 4000m/8000m, 3400, 3500, 5300, 5400 2.Advanced experience with configuration and support of Juniper equipment. 3. Advanced experience with configuration and support of Alcatel-Lucent equipment. ? Strong layer 2 and layer 3 experience with a focus on enterprise and data center switching and routing including: Ethernet, Spanning Tree, VLAN, MPLS, Link Aggregation, ether-channel, QoS, 802.1Q, DHCP, ARP, RARP, IGMP, SNMP, IPv4, VoIP, multicast routing protocols, 10 Gig Ethernet, minimum 5 years ? Demonstrated ability to gather design requirements or problem requirements and recreate infrastructure so that initial design validation can be completed or in the case of a problem being able to troubleshoot and isolate root cause. ? In-depth knowledge of network element infrastructure, error reporting, OS limitations, etc. ? Strong Customer interface skills ? Excellent written and communication skills ? Experience in mentoring peers and junior level engineers and administrators ~cb~8/31/2009
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
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	Columbia	MD	11/20/2009
Sr. Systems Design Engineer
The position requires a BSEE/MSEE with emphasis in digital signal processing (DSP). Must have proven ability to use computer tools for simulation, coding and measurement (i.e. MatLab) and working knowledge of C and/or C++ languages within Microsoft Windows? and Linux operating system frameworks. Ability and desire to work on rapid paced projects with several design tasks. Ability to work effectively as a member of a geographically dispersed team of engineers both in our core labs and in other functional areas including our sales group. Chosen candidate must have excellent communication skills, both verbal and written. Must be willing to travel when necessary. ? Must be a US Citizen ? High-level government security clearance is required Desired Skills: ? MSEE with emphasis in communications signal analysis and processing ? In-depth knowledge of programming with Visual Studio? and Wind River DIAB development environments ? Experience in design of demodulators including digital PLL's, digital filters and bit coding/decoding algorithms ? In-depth knowledge of complex receiver and signal processing chains ? Working knowledge of the Agilent E3238s system ? Knowledge of measurement techniques and considerations in the wireless market ? Working knowledge of direction finding
Agilent Technologies, Inc. US	Santa Clara	CA	11/20/2009
R&D Bioinformatics, Software Engineer
External Qualifications: This dynamic position requires a MS degree in Computer Science or equivalent plus a minimum of 5+ years relevant experience with bioinformatics tools and procedures as applied to high-throughput computational pipelines. Chosen candidate must have the following: ? 5+ years experience in C++, .NET, and Java ? Object oriented programming experience a plus ? Experience with: BLAST, BLAT and/or MOST ? Experience with SQL and/or Oracle database ? Knowledge of public biological databases, tools, and repositories is required ? Hands-on experience producing software in collaborative, multidisciplinary environment to solve problems in biological or other life science is highly desirable ? Experience with Image Analysis is a plus Geographic Location: Bay Area, California (Santa Clara) ~cb~10/19/09
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	Colorado Springs	CO	11/20/2009
R&D Software Engineer
Position requires: ? BS/MS Degree in Computer Science or equivalent and a minimum of 5+ years SW development experience ? 5+ yrs Java Development, with a significant portion of this in the client server area. ? Experience with Object and data modeling ? Experience with WEB application development ? Experience creating UI?s using FLEX Builder. ? Experience working with XML and XSD?s. ? Experience with database access and database design. ? Excellent verbal and written communication skills ? Ability to work with cross-functional global teams ? Results-oriented and track record of success in delivering to critical project deadlines ? Strong sense of initiative and ability to work autonomously These additional skills are strongly preferred: ? Network protocol knowledge and experience ? Experience with multi-threaded transaction systems ? Linux OS experience ? Telecom or general networking industry knowledge is helpful ( as related to network quality of service) ? Web based transactions (managing sessions, persistence of the data, JPA) ? Knowledge of, REST API, GUI human factors background is an added plus ? C++ programming ? Prefer experience will some or all of the following: JUnit, MySql, Hibernate, JMS, XML and Java parsers, J2EE, JTA, JMX, Java Patterns. ~cb~8/18/2009
Agilent Technologies, Inc. US	Santa Clara	CA	11/20/2009
Software Engineer
Educated to at least university degree level, you'll also have 5+ years' practical R&D experience, including at least 3 years' in a similar environment. A keen problem-solver with a proactive, team-oriented approach, you'll relish the challenges this pioneering environment presents. ~cb~10/29/09
Agilent Technologies, Inc. US	Santa Clara	CA	11/20/2009
Software Engineer
Educated to at least university degree level, you'll also have 5+ years' practical R&D experience, including at least 3 years' in a similar environment. A keen problem-solver with a proactive, team-oriented approach, you'll relish the challenges this pioneering environment presents. ~cb~10/29/09
Agilent Technologies, Inc. US	Santa Clara	CA	11/20/2009
Senior Software Engineer
Job requirements: ? Demonstrated C/C++ programming skills in a product-development environment. ? Demonstrated knowledge of STL, MFC, ATL, ActiveX, and other related software technologies. ? Experience with Microsoft Visual Studio and other software-development tools required. ? Experience investigating newer technologies and evaluating feasibility of utilizing newer technologies for system platforms. ? Experience synthesizing a cohesive system consisting of hardware, electronics, firmware, and software. ? Ability to work collaboratively in team environments. ? Ability to provide clear and concise oral and written communication of product concepts and engineering requirements. ? Ability to follow both written and verbal directions and ask questions when necessary. ? Ability to adhere to a quality control system. ? Willingness to exercise considerable independent judgment. ? Demonstrated strong follow-through with thorough attention to detail. Education/Experience: ? Bachelor's degree in computer science, engineering, or related field. Advanced degrees are strongly preferred. ? 10+ years of technical experience required, with past work on product-development teams strongly preferred. ? Experience developing production-quality software required, with robotics and automation experience a plus. ~cb~10/29/09
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
Customer Account Specialist
? Bachelor of Arts or Bachelor of Science degree ? Ability to travel ? Relevant customer experience Geo Location: Wilmington, DE ~cb~11/11/09
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	Santa Rosa	CA	11/20/2009
Productivity Engineer
Musts - 5 years minimum experience in PCB layout - 3 years minimum experience in high-speed digital and/or high-frequency RF PCB layout - Expertise with Mentor Graphics Expedition and specifically Expedition CES - Expertise in manufacturing output processes, data, and tools - Experience with Mentor BoardStation layout - Excellent troubleshooting skills and ability to trace problems to root cause in layout - Knowledge and familiarity with PCB fabrication and assembly technologies and processes - Experience with the Valor design rule checker - AS degree in electronics, Computer-Aided drafting, or equivalent - Excellent communication skills and ability to do multitasking - Good computer skills Wants Skill or experience in the following areas would be a plus, but aren't required. - Programming skills in scripting (e.g., VBscript, Perl, Javascript) - Documentation and technical writing skills - Familiarity with component library and schematic tools - Electronic circuit design experience - Familiarity with other PCB tools besides Mentor Graphics (e.g., Cadence, Zuken, Intercept) and can objectively evaluate and recommend best tools and practices - Experience in systems and EDA tool administration - Bachelors degree in electrical engineering or equivalent ~cb~11/17/09
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)	Columbus	NE	11/20/2009
Business Analyst
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
Core Team Leader- R&D Platform
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BD (Becton, Dickinson and Company)	Sandy	UT	11/20/2009
Engineering Technician
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BD (Becton, Dickinson and Company)	Research Triangle Park	NC	11/20/2009
Global Business Systems Analyst -Manufacturing Execution System Implementation
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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)	San Diego	CA	11/20/2009
Instrumentation Technician I
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BD (Becton, Dickinson and Company)	Broken Bow	NE	11/20/2009
Intern -Engineering Process/Electrical
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BD (Becton, Dickinson and Company)	Sumter	SC	11/20/2009
Lead Technical Associate
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BD (Becton, Dickinson and Company)	Sumter	SC	11/20/2009
Lead Technical Associate
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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)	Wilson	NC	11/20/2009
Manufacturing Engineer
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
Manufacturing Integrator, Diabetes Care
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BD (Becton, Dickinson and Company)	Sandy	UT	11/20/2009
Mechanical Design Engineer, Medical Surgical Systems
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BD (Becton, Dickinson and Company)	Baltimore	MD	11/20/2009
Mechanical Engineer / Senior Mechanical Engineer
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BD (Becton, Dickinson and Company)	Sandy	UT	11/20/2009
Mechanical Engineer w/ FEA, Medical Surgical Systems
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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
Molding Technology Engineer
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BD (Becton, Dickinson and Company)	Columbus	NE	11/20/2009
PosiFlush Manufacturing Engineer
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
Principal Engineer - Technical Lead
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
Principal Engineer, Environmental Packaging
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
Principal Engineer, Mechanical Engineer - Hypodermic team
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
Principal Engineer- R&D Platform
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BD (Becton, Dickinson and Company)	Sandy	UT	11/20/2009
Principal Scientist, Advanced Technology - Medical Surgical Systems
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BD (Becton, Dickinson and Company)	Canaan	CT	11/20/2009
Process Engineer - Molding
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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)	Waltham	MA	11/20/2009
Production Operator II
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BD (Becton, Dickinson and Company)	Wilson	NC	11/20/2009
Production Planner/Buyer
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
Project Engineer
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BD (Becton, Dickinson and Company)	Durham	NC	11/20/2009
Project Engineer - Packaging
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BD (Becton, Dickinson and Company)	Columbus	NE	11/20/2009
PS Site IT Leader
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BD (Becton, Dickinson and Company)	San Jose	CA	11/20/2009
QA Technician II -FPR
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BD (Becton, Dickinson and Company)	Sandy	UT	11/20/2009
Quality Engineer
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BD (Becton, Dickinson and Company)	Burlington	NC	11/20/2009
Quality Engineer II, Reagents
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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)	Baltimore	MD	11/20/2009
R&D Electrical Project Engineer
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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)	Baltimore	MD	11/20/2009
R&D Mechanical Project Engineer
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BD (Becton, Dickinson and Company)	Baltimore	MD	11/20/2009
R&D Sr. Optical Engineer
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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)	Mebane	NC	11/20/2009
Research & Development Validation Engineer II
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
Senior Engineer, Packaging Technology, BD Medical Surgical Systems
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
Senior Project Engineer - Assembly
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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)	Holdrege	NE	11/20/2009
Six Sigma Coordinator
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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. Manufacturing Equipment Engineer - Reagents
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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
Staff Engineer, Packaging Technology
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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)	Columbus	NE	11/20/2009
Summer Engineering Internship
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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)	Wilson	NC	11/20/2009
Tech Transfer Engineer
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BD (Becton, Dickinson and Company)	Durham	NC	11/20/2009
Technical Team Member- ADVANCED MOLDING SKILLS
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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)	Wilson	NC	11/20/2009
Validation Engineer
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BD (Becton, Dickinson and Company)	Wilson	NC	11/20/2009
Validation Technician II
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BD (Becton, Dickinson and Company)	Franklin Lakes	NJ	11/20/2009
WW Senior Strategic Marketing Manager
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