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document control in San Diego

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    1. Senior Medical Writer

      Sigma Bullhorn ID: 7963Location: La Jolla Area, CAPosition: Senior Medical WriterClient Industry: Biotechnology/PharmaceuticalsClassification: 4 Months Contract (Extensions Likely Into 2016 or Conversion to FTP Status) PLEASE NOTE: Remote Work is NOT allowed. On-Site Only. If you have any questions, I’ll be happy to answer them, but I’ll need to see a copy of your most ‘up-to-date’ resume to ...

    2. Document Control Associate, San Diego, CA

      Document Control Associate, San Diego, CA Kelly Scientific Resources, a division of Kelly Services, has an immediate opening for a Document Control Associate with a growing biotech company located in a state-of-the-art facility in San Diego, CA. Position Overview: The Document Control Associate is expected to have a working knowledge of Good Laboratory Practices GLP as well as to ensure ...

    3. Companion Diagnostic Development Director - San Diego, CA

      Newly founded biotech company seeking individual with proven success leading efforts for companion diagnostic or clinical trials in collaboration with oncology therapeutic trials. Functions: *** Create clinical trial protocols, case report forms, study reports and clinical data listing for trials. *** Oversee development and approval of biomarkers for drug efficacy and patient selection ...

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    4. Research Associate

        Hello,   My name is Josh and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Research Associate for a prominent Fortune 500 client of ours.  This position is located in San Diego CA.  Details for the positions are as follows:   Job Description We are seeking a highly motivated scientific associate with laboratory experience to join the ...

    5. Technical Editor/Marketing Assistant

      Technical Editor/Marketing Assistant Position Summary The Technical Editor/Marketing Assistant works alongside technical staff, senior management, and Pangea’s subcontractors as well as client staff, providing editing, formatting and production support for all documents produced by Pangea. Company documentation ranges from highly technical memorandums and reports, environmental documents, ...

    6. Senior Regulatory Medical Writer

      Senior Medical Writer (Remote) Job Responsibilities: Responsible for writing and editing documents including, but not limited to, investigator brochures, integrated clinical/statistical study reports, clinical protocols and amendments, Integrated Summaries of Safety (ISS) and Efficacy (ISE), annual reports/DSURs, manuscripts and posters Develop, maintain and drive document finalization ...

    7. Commissioning & Qualification Validation Consultant -

      ProPharma Group has a client in San Diego that is designing and installing a new chemical bulk storage and distribution tank farm. They need a professional consultant with CQV and tank system experience to help them write and possibly execute the following types of technical documentation: FATs, URSs to IQ/OQ. The project entails 1X 1000 gal. acid tank, 1x2000 gal caustic tank, 1x1000 gal. ...

    8. Synthesis Manager

      Our client, an exciting biotech company, is seeking a Synthesis Manager to join their team in Vista, CA. RESPONSIBILITIES Plan and manage GMP process and manufacture activities Ensure synthesis department is following approved GMP manufacture directions such as Master Batch records, Standard Operating Procedures, Standard Test Procedure and other procedures to manufacture GMP material, ...

    9. Quality Engineer (Req: 4258367)

      Kelly Scientific, a division of Kelly Services, is actively recruiting for a Quality Engineer for a major biotech company in Carlsbad, California. Essential Duties and Responbilities: Working with GMP Compliance team to rescope Frederick site procedures to include R&D lab and address any identified compliance gaps. Good understanding of FDA 21 CFR 820 or 21 CFR 210/211 Strong Document ...

    10. Validation Engineer

      Validation Engineer - Regulated Environment At Formex, we are a group of competent individuals, fiercely committed to Collaboration and Possibility. By living our values of Leadership, Execution and Accountability, we work together as a team to advance our client’s drug compounds, partnering to bring products from ideas into existence. We have an immediate opening for a skilled and ...

    11. Scientist II - Molecular Biologist, Carlsbad, CA

      Scientist II - Molecular Biologist, Carlsbad, CA Kelly Scientific Resources, a division of Kelly Services, has an immediate opening for a Scientist II to work with a world-class, leading biotech company in the Carlsbad, California area! As a Scientist II you will work in a team-based environment and perform Quality Control assays/experiments on molecular biology reagents bulks, components, ...

    12. Scientific Associate - Molecular Biology

      Hello,   My name is Steve Graham and I represent The Fountain Group.  We are a national staffing firm and are currently seeking a Scientific Associate- Molecular Biology for a prominent client of ours.  This position is located in San Diego, CA. Details for the position are as follows:   Job Description: We are seeking a highly motivated scientific associate with 0-3 years of biopharma ...

    13. Global Validation Leader

       Be responsible to drive the Facility, Equipment & Instrument, Software, and Process Qualification initiative for the company Responsible for the development of the master plans and the entire qualification execution at the new Tatabanya location and interacts functionally across the organization at San Diego and Tatabanya.  Develops and writes the Qualification Master Plans, protocols, ...

    14. Microbiologist for a Biotech Company

      Our client is seeking an experienced Microbiologist for its San Diego facility. The Microbiologist is responsible for designing, directing, and executing the research plans and experimentation in microbiology.  Involvement in testing new methods compatible with molecular based pathogen tests and designing validation plans for the AOAC studies. Other responsibilities include supervising a ...