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    1. 98211 Clinical and Regulatory Analyst III (2 year contract)

      Job Description:Qualifications:This position in Global Safety requires a Bachelor's degree, preferably in nursing, pharmacy or a biological science.At least three years of experience in a hospital, pharmaceutical, or research position.Prior experience in coordinating and overseeing the production of Aggregate Reports (PSUR, DSUR, PAER etc.) and RMPs required.PSUR authoring experience would be ...

    2. Regulatory Affairs Associate - CMC

      Regulatory Affairs Associate – CMC: Near Edgewater, NJ area Position Overview Regulatory Affairs Specialist – CMC: Ensures regulatory compliance by determining submission requirements for development projects and review of CMC changes to current marketing applications. The Regulatory Affairs Associate Director – CMC is also responsible for providing information to cross-functional team ...

    3. Regulatory Affairs Associate - CMC

       Regulatory Affairs Associate – CMC: Near Edgewater, NJ area   Position Overview Regulatory Affairs Specialist – CMC:  Ensures regulatory compliance by determining submission requirements for development projects and review of CMC changes to current marketing applications.  The Regulatory Affairs Associate Director – CMC is also responsible for providing information to cross-functional ...

    4. Biologist

      Job Summary: Seeking a highly motivated biologist with at least 5 years of industry experience to join the in vitro biology team working for a client located in Cranbury, New Jersey. This vital position will independently design and execute studies to advance new small-molecule drug candidates in the Oncology portfolio. Responsibilities will include developing, characterizing, and running ...

    5. Process Engineer / Consumer Products / Pharma

       Process Engineer: Description A Global Leading, multi-billion dollar, Consumer Products Company, has an immediate need for a Process Engineer based in Skillman, NJ. This is a great opportunity to work on a portfolio of some of the World’s most recognized and trusted Brands. Responsible for the site transfer of products, packaging components and/or raw materials on currently marketed ...

    6. Medical Writer

        Medical Writer Responsibilities: · Writing, editing, reviewing and formatting documents that conform to domestic and/or international regulatory submissions and internal document standards, while meeting project timelines. · Carries out core-level responsibilities with minimal supervision. · Responsible for ensuring that assigned documents undergo a quality check before approval, and ...

    7. CMC Manager (428863)

      OVERVIEW   Responsible for planning, authoring, and reviewing Chemistry, Manufacturing, & Controls (CMC) content of global Clinical Trial Applications (CTAs) for biopharmaceuticals and small molecules for all phases of clinical development. Responsibilities include providing CMC content of initial CTAs, Quality Amendments, DMFs, health authority responses, meeting briefing packages, BLAs, ...

    8. QUALITY ASSURANCE - ASSISTANT DIRECTOR - COMBINATION PRODUCTS

      (Need 2 of these people) QUALITY ASSURANCE - ASSISTANT DIRECTOR, COMBINATION PRODUCT Chicago, Il FULL RELO DESCRIPTION The R&D GMP Quality, Clinical Product Supplies, organization is responsible for Product Quality Assurance for investigational medicinal products (IMP), including both pharmaceutical drug and drug/device combination products. These activities comprise of disposition ...

    9. Procedure Author

        TrueBridge Resources, a North Highland company, ranked 4th among the fastest-growing staffing firms in the U.S. for 2013 and 2014 by Staffing Industry Analyst magazine.  We work with clients to fill Contract, Contract-to-Hire, and Direct Hire opportunities within Management Consulting, IT, Accounting/Finance, Human Resources, and Marketing areas.   Bridge your career to the next level and ...

    10. Quality Engineer I

      Hello,   My name is Domenic and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Quality Engineer I for a prominent client of ours.  This position is located in Skillman, NJ. Details for the position are as follows:   Job Description:   Detailed Job Description: Candidate for a Marketed Product Stability (MPS) position for North America ...

    11. In Vivo Drug Discovery Scientist, Pharmaceutical (97854)

      Job Description: In Vivo Drug Discovery Scientist is needed for a contract position at major pharma company in Northeast.  Conduct in vivo physiology experiments to support drug discovery programs within the Department of Cardiovascular Disease. The successful candidate will support in vivo model development activities. Responsibilities will include: the execution of in vivo studies in to ...

    12. Data Management Subject Matter Expert (SME)

      TrueBridge Resources, a North Highland company, ranked 4th among the fastest-growing staffing firms in the U.S. for 2013 and 2014 by Staffing Industry Analyst magazine.  We work with clients to fill Contract, Contract-to-Hire, and Direct Hire opportunities within Management Consulting, IT, Accounting/Finance, Human Resources, and Marketing areas.   Bridge your career to the next level and ...

    13. Food Technologist

      We are seeking a highly motivated R&D Technologist to join a growing highly successful business, Premio Foods’ Research and Development team. The Technologist will be responsible for performing product development work to meet project objectives, supporting innovation and brand maintenance initiatives. Must be able to perform multiple, simultaneous projects. Our mission is to improve the ...

    14. QC Scientist- Pharmaceutical (Lakewood, NJ)

      Scientist I Department: QC ChemistrySUMMARY: Provide technical support for routine testing activities and conduct physical and chemical analysis of samples, products and materials. Primarily responsible for technical transfer and validation of methods to support QC testing of products and materials. Identify basic technical problems, atypical test results or methodology malfunctions and ...

    15. CMC Regulatory Scientist III

      *Please note that this is a 6 month contract assignment. Candidates cannot start an assignment until background check and drug test is completed* Responsibilities: Provide regulatory CMC filing support for assigned projects/products by providing required CMC submission activities (planning, obtaining required data, coordination, authoring, reviewing, and submission) in accordance to ...

    16. Study Manager

      Study Manager  Functional Area: Clinical Research The Study Manager is responsible for coordinating the functional team members and their activities across all geographies, liaising with the sponsor to ensure that the study deliverables are met following proper conduct of a clinical study, including compliance with International Conference on Harmonisation (ICH) Harmonised Tripartite ...

    17. Scientist I - Research Technician - Skillman, NJ

      Every day, Kelly Services connects professionals with opportunities to advance their careers. We currently have an exciting contract opportunity for a Scientist (Level I) with a pharmaceutical company located in Skillman, NJ. Work schedule will be Monday - Friday, typically 8a - 5p. Fulltime, 40 hour work week. Duration is for one year with possible extension, however no guarantee. Pay rate ...

    18. Chemist

      Chemist   Overview: The Chemist is responsible for performing analytical testing of components (where necessary), raw materials, pre-mixes, blends, bulk product and stability product in order to assure compliance to approved specifications.  Responsibilities: Conduct critical chemical and physical analyses on raw materials, initial, in-process and final products, and stability ...

    19. Bioanalytical Manager and Scientist jobs

        Bioanalytical positions in NJ and Utah Lab Director, Scientist and Project Manager / Principal Investigator jobs – all with Lc/ms/ms   1. Bioanalytical Sr. Scientist Project Manager Working as a scientist you will provide our sponsors with a single point of contact, handling all technical and commercial aspects of their relationship with company from initial quote, through method ...