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regulatory affairs in Los Angeles

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    1. Global Scientific Communications Manager-1285

      What are the top 3 skill sets needed to qualify for this opening? Scientific acumen, ability to work under pressure, strong communication skills Global Scientific Communications Manager - Bone Health Therapeutic Area Job Description: The successful candidate will be ...

    2. Regulatory Affairs (1890)

      Responsible for formatting of regulatory submission documents ensuring that documentation meets Client's submission-ready standards under direct supervision. Essential Duties and Responsibilities • Provides support and technical assistance for formatting regulatory ...

    3. NURSE IV- Evaluation Manager

      This position is with the Department of Veterans Affairs (VA), Veterans Health Administration (VHA), in the Office of Academic Affiliations (OAA), in Washington, DC. The Department of Veterans Affairs (VA) Nursing Academic Partnership Program (VANAP) has been developed to ...

    4. Regulatory Affairs Specialist III

      Summary: Responsible for preparing submissions to both national and int’l regulatory agencies, including preparation, submission, and periodic update of drug master files and related correspondence and letters of authorization. Also responsible for providing technical data ...

    5. Regulatory Affairs (4379)

      Responsible for formatting of regulatory submission documents ensuring that documentation meets Client's submission-ready standards under direct supervision.  Essential Duties and Responsibilities • Provides support and technical assistance for formatting regulatory ...

    6. TECHNICAL DIRECTOR (biopharmaceutical)

      We are looking for a Systems Director, Sales, Marketing and Business to work on-site at a leading biopharmaceutical company in Thousand Oaks, CA. In this full time position, you will support the organizational functions and business processes focused around, but not limited ...

    7. 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 ...

    8. Medical Writer (4350)

      Summary: This position will be responsible for assisting in developing the strategic medical communications platform for the therapeutic area in collaboration with various cross-functional stakeholders. This medical communications platform will then be incorporated across ...

    9. Specialist Clinical Supply Chain

      Supply chain experience (any industry, but pharma or biotech is a plus) including demand and supply planning; SAP experience is a plus (but not required), strong organization and multi-tasking skills are REQUIRED, strong Excel skills, strong analytical and problem-solving ...

    10. Quality Control Publisher I

      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: Quality Control Publisher I Industry: Biotech ...

    11. Regulatory Compliance Specialist

      Regulatory Compliance Specialist for Custom Chemical Formulators Inc. (CCFI) – Santa Fe Springs, CA Custom Chemical Formulators, Inc. (CCFI) is a family-owned and operated premier industrial chemical manufacturer and supplier for the Industrial, Institutional, Janitorial, ...