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  1. Sr. Principal Scientist - Microbiology (Manufacturing Experience Required) at firstPRO Inc.

    Operations, Manufacturing/Materials Management, Supply Chain, Corporate and Plant Quality, Manufacturing, Regulatory Affairs, Marketing, Finance, Executive...

  2. Regulatory Affairs Specialist at The Richmond Group USA

    So if you are an experienced regulatory affairs professional ike working in a collaborative environment, and have solid familiarity with medical devices, you...

  3. Director, Regulatory Affairs at Sterling Hoffman Life Sciences

    Prepare regulatory filings and maintain regulatory requirements. Preference will be given to people with recent experience in regulatory affairs management....

  4. Compliance Engineer, Medical Devices (Life Sciences), Google[x] at Google

    Prepare documentation of medical device design projects and communicate with internal regulatory affairs personnel to support global clearances/approvals....

  5. Medical Device Functional Safety / Software Safety Expert at Tuv America

    Perform evaluations of regulatory submissions including:. TÜV SÜD America Inc., a global leader in product safety and EMC testing, regulatory affairs and...

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    1. Associate Regulatory Affairs

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: Regulatory Affairs AssociateJob ID: 1762Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 18 Month ContractPay Rate Range: Depends on Experience (W-2 all ...

    2. Global Director, Regulatory Affairs

       The Global Director of Regulatory Affairs will direct all Regulatory Affairs activities and will have responsibility for providing significant input regarding worldwide strategy, planning, execution and budget. This individual takes the lead to develop, propose and implement regulatory strategies for new products, changes to existing commercial products and new indications. This key position ...

    3. Regulatory Affairs Manager - (97716)

      A highly reputable pharmaceutical corporation is looking for a qualified Regulatory Affairs Manager to work in Thousand Oaks, CA.Job Description:The Regulatory Affairs CMC Product team is responsible for execution and/ or coordination of all global regulatory CMC activities, including providing leadership, guidance, and insight to oversee the successful execution and implementation of ...

    4. CMC Regulatory Affairs Manager - Biotech/Pharma

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis. Title: CMC Regulatory Affairs ManagerJob ID: 1687Industry: Biotech/PharmaceuticalLocation: Thousand Oaks, CADuration: 6 Month ContractPay Rate Range: Depends on Experience (W-2 all ...

    5. Regulatory Affairs Associate

      Under general supervision responsible for the coordination and the preparation of documents/packages for regulatory submissions. Review and evaluate technical and scientific data and reports required for submission in support of companies products.Responsibilities:• Track of status and progress of regulatory documentation • Review, edit and proofread regulatory documentation • Assist in ...

    6. Associate Regulatory Affairs

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: Associate Regulatory Affairs Job ID: 1735 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 5 Month Contract Pay Rate Range: Depends on Experience (W-2 ...

    7. Regulatory Affairs (Publishing) Associate (3704)

      Summary: Under direct supervision and responsible for the systems preparation of components, building, validating, quality review, submission to the regulatory authority(ies) and archiving of regulatory dossier in support of client's products. Essential Publishing Duties and Responsibilities: • Working knowledge of ICH Submission Readiness Standards • Supports the compilation of ...

    8. Global Director / Manager Regulatory Affairs

      The Global Director / Manager of Regulatory Affairs will direct all Regulatory Affairs activities and will have responsibility for providing significant input regarding worldwide strategy, planning, execution and budget. This individual takes the lead to develop, propose and implement regulatory strategies for new products, changes to existing commercial products and new indications. This key ...

    9. Regulatory Affairs Manager

      • TOP 3 SKILL SETS: Scientific background, Experience with Regulatory Affairs Chemistry Manufaturing and Controls , Experience in working with document management systems ( EPIC) (IMR) including Microsoft Suite.  • DAY TO DAY RESPONSIBILIES / FIRST 30 DAYS: Execution of regulatory filings (ARMC’s, Annual Notifications, CTA Amendments, and Post Approval Changes).  • RED FLAGS: Only clinical ...

    10. Regulatory Affairs Associate

      Kelly Clinical Research is seeking a Regulatory Affairs Associate for a contract opportunity in Westlake Village, CA. The Regulatory Affairs Associate will be responsible for formatting regulatory submission documents ensuring that documentation meets the company submission-ready standards under direct supervision.Essential Duties and ResponsibilitiesConvert MS Word documents in a legacy ...

    11. CMC Regulatory Affairs Manager

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: CMC Regulatory Affairs Manager Job ID: 1687 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 6 Month Contract Pay Rate Range: Depends on ...

    12. CMC Regulatory Affairs Manager

      Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.   Title: CMC Regulatory Affairs Manager Job ID: 1687 Industry: Biotech/Pharmaceutical Location: Thousand Oaks, CA Duration: 6 Month Contract Pay Rate Range: Depends on ...

      1. Animal Originated Tissue Expert at Tuv America

        Perform evaluations of regulatory submissions including:. Perform regulatory audits of clients per European Medical Device Directives (AIMD, MDD, IVDD),...

      2. Cardiac Implant Expert at Tuv America

        Perform evaluations of regulatory submissions including:. TÜV SÜD America Inc., a global leader in product safety and EMC testing, regulatory affairs and...

      3. Director of Quality, Safety, Accreditation & Risk at Southern Maryland Hospital Center, Inc.

        Master's Degree 3-5 years experience required MedStar Southern Maryland Hospital Center is actively recruiting for a outstanding candidate for Director of

      4. Legislative & Regulatory Affairs Director - 90188035 - Washington at Amtrak

        Government Affairs || Corporate. The Director, Legislative & Regulatory Affairs, develops, guides and directs legislative policies and proposals to advance...

      5. Clinical Trial Research Physician at Laulima Government Solutions, LLC.

        Knowledgeable in the areas of clinical research and regulatory affairs as they relate to clinical studies and healthcare management....