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    1. 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 ...

    2. 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 ...

    3. 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 ...

    4. 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 ...

    5. 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 ...

    6. 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 ...

    7. 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 ...

    8. 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 ...

    9. 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 ...

    10. 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 ...

    11. 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 ...

    12. Regulatory Affairs Manager, EPA

      Regulatory Affairs Manager, EPA - Near Jersey City, NJ   The Regulatory Affairs Manager is responsible for managing the Regulatory Affairs department. This individual will work with cross functional departments to ensure that all products are in compliance with the appropriate government agency requirements. He/she will represent Regulatory in project team meetings and provide the relevant ...

    13. Regulatory Affairs Manager, FDA

      Regulatory Affairs Manager, FDA - Jersey City, NJ area Handles day-to-day regulatory affairs matters and regulatory compliance relating to new food, treat and consumable product development and existing product lines coordinating such effort with relevant stakeholders such as Legal, QA, Marketing, Packaging and R&D departments. The Regulatory Affairs Specialist provides updates on existing ...

    14. Biosample Clinical Manager

      Hello,   My name is Domenic and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Biosample Clinical Manager for a prominent client of ours.  This position is located in East Hanover, NJ. Details for the position are as follows:   Job Description:   Duties: Support individual clinical trial teams (CTTs) and Biomarker Sub-teams as required ...

    15. Associate Director Compendial Affairs

       Our client, one of the world's largest drug firms, is seeking an individual to lead the Compendial (USP/EP/JP) review and submission processes as well as providing strategic guidance on impact of Compendial changes to Global Testing standards and documentation for QC testing of all company-manufactured products. This oversite includes new product launches, scale-ups, CMC guidance from a QC ...

    16. Head of Formulation Development

      Head of Formulation DevelopmentKelly Scientific has partnered with an esteem specialty generic pharmaceutical company in Central NJ This position is responsible for independently creating and implementing formulation development strategies. The Formulation head within team based structure and provides direction for the progress of team projects. Serves as an SME (subject matter expert) in ...

    17. Regulatory CMC Associate Manager - NJ - 6 months (97610 - KD)

      Assist and support regulatory CMC managers in the following activities: Defining global CMC regulatory strategy and decisions for development projects or marketed products to achieve optimal submission/approval results and ensure regulatory compliance. Communicating CMC regulatory strategy, key issues and remediation activities needed throughout the project/product life cycle, to project ...

    18. CMC Manager Regulatory

      This is a 1 year renewable contract position.   Minimum Requirements:   MS or PhD in a biological science or a related field required a minimum of 5 years of industrial/regulatory experience in biologics development and/or manufacturing Experience in writing regulatory CMC filings required. Must have experience in monoclonal antibody or biologics development. Pre-approval ...

    19. CMC Regulatory Manager

      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, NDAs, ...

    20. GLP Quality Assurance Specialist

      Kelly Scientific is seeking a Quality Assurance Lab Technician with strong Lab experience and excellent GLP knowledge. The incumbent must will perform a variety of tasks in the lab and all in conjunction with GLP standards.Experience / Training / Education: Bachelor's degree in Biology, Chemistry, or science related field. At least 2 years of experience in QA or QC, with focus on bio ...

    21. Quality Engineer – Process and Validation

      Experience: Minimum of three (3) years’ relevant experience performing validation activities within an aseptic pharmaceutical environment.   Education: Bachelor’s degree or higher in Engineering, Life Sciences or related discipline (Engineering, Chemical Engineering, Chemistry, Biology, etc.)   Familiarity with current industry practices and guidelines including those required / ...

    22. Quality Engineer - Utility and Facility Validation

      Experience: Minimum of three (3) years’ relevant experience performing utility and facility qualification/validation activities within a pharmaceutical, diagnostic, biotechnical, or chemical processing environment. Experience within an aseptic manufacturing and processing plant is preferred.   Education: Bachelor’s degree or higher in Engineering, Life Sciences or related discipline ...

    23. Bioinformatics Analyst

        Bioinformatics Analyst - Princeton, NJ area Our client is a Princeton, NJ area biotech company. The Bioinformatics Analyst analyzes experimental data, manipulates and interprets large data sets in accordance with established protocols. Provides routine molecular biology support to the Analytical Services Group. Provides principal support to generation and analysis of gene expression, ...

    24. Director, Medical Science

      Director, Medical Science, Summit NJ area MUST HAVE MD-PLEASE DO NOT APPLY IF NOT AN MD SUMMARY The Director of Medical Science (MS) is responsible for providing input into the Global Project Teams in planning, designing, developing, executing and interpreting clinical studies, including but not limited to those carried out in North America (NA) the global development program. The ...