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regulatory affairs in Los Angeles

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    1. Regulatory Affairs Associate (3573)

      Responsible for converting and formatting of regulatory submission documents ensuring that documentation meets client's submission-ready standards under direct supervision. Essential Duties and Responsibilities: • Convert MS Word documents in a legacy format to ISIWriter ...

    2. Quality Assurance & Regulatory Affairs Associate/Specialist

      Summary: This individual reports to the QARA Manager and performs assigned tasks and responsibilities including medical device and product registrations, preparing Technical Files (DMRs), maintaining QMS documents, assisting internal audit, performing regulatory research ...

    3. Senior Regulatory Affairs Specialist

      Working with minimal supervision, manage complex projects/products, including responsibility for the content, assembly, pre-final review, and filing of major medical device applications (e.g., IDEs, PMAs, 510(k)s) submitted to the FDA and foreign regulatory agencies. Applies ...

    4. Regulatory Affairs Associate (3573)

      Responsible for converting and formatting of regulatory submission documents ensuring that documentation meets client's submission-ready standards under direct supervision. Essential Duties and Responsibilities: • Convert MS Word documents in a legacy format to ISIWriter ...

    5. Regulatory Affairs Associate (3573)

      Responsible for converting and formatting of regulatory submission documents ensuring that documentation meets client's submission-ready standards under direct supervision. Essential Duties and Responsibilities: • Convert MS Word documents in a legacy format to ISIWriter ...

    6. Regulatory Affairs Coordinator

      For 60 years, Kelly Services has provided outstanding employment opportunities to the most talented individuals in the marketplace. Today, we are proud to offer a contract Regulatory Affairs Coordinator position for a top Medical Device company in Diamond Bar, CA JOB TITLE: ...

    7. Regulatory Affairs Manager, RA CMC Product Lead

      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 Manager, RA CMC Product Lead ...

    8. Regulatory Affairs Mgr-1577

      •WHY IS THE POSITION OPEN? Maternity leave cover •TOP 3 SKILL SETS: -Significant amount of regulatory CMC hands on experience (5 years+), ideally including for biotech products -Expertise in use of document management systems eg EDM, DECADE, EPIC -Self motivated, independent ...

    9. Regulatory Affairs Mger-1499

      This is a 5-6 month contract position for a Regulatory Affairs Mger. Looking for candidates to interview asap. WHY IS THE POSITION OPEN? Candidate will be the contact for the FDA and will support marketed and development products. Working with teams to review and assess ...

    10. Regulatory Affairs Specialist | Chemical

      Kelly Scientific is actively recruiting for a Regulatory Affairs/ Regulatory Compliance Specialist for a Chemical Manufacturer in Santa Fe Springs. This is an exciting opportunity for a recent college graduate with a B.S. in Chemistry. Our client is looking for someone eager ...

    11. Regulatory Affairs Manager (IND applications)

      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 Manager Job ID: 1499 Industry ...

    12. REGULATORY AFFAIRS MANAGER

        REGULATORY AFFAIRS MANAGER   Simply Biotech specializes in recruiting exclusively for the biotech community. We are currently seeking a Regulatory Affairs Manager for a leading and growing biotech firm in Irvine, California. Relocation assistance may be available.   ...