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  1. Clinical Data Analyst at ICON Clinical Research

    Work with Data Management, Clinical Operations, Central Laboratory, ITG, Biostatistics, Medical Writing, Regulatory Affairs and Quality Assurance to ensure all...

  2. Sterilization and Microbiology Auditor / 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. Quality Management System Auditor at Tuv America

    TÜV SÜD America Inc., a global leader in product safety and EMC testing, regulatory affairs and certification, has an immediate opening for a Quality Management...

  4. Medical Device Auditor at Tuv America

    TÜV SÜD America Inc., a global leader in product safety and EMC testing, regulatory affairs and certification, has an immediate opening at our offices in the...

  5. Pressure Vessel Engineer / Auditor at Tuv America

    TÜV SÜD America Inc., a global leader in product safety and EMC testing, regulatory affairs and certification, has an immediate for:....

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    1. Jr. Machining Process Engineer

      Jr. Machining Process Engineer Company Job Location: Chicago, IL Salary: $80,000 - $100,000 Relocation Fee Provided. This part will focus on advances related to crushing and machining schedules used as a touch of the helpful contraption industry, for instance, think less squashing, and profile beating, arranging, recommending, and etc. Obligations: Distinguish, arrange and execute ...

      1. Manager, US Regulatory Affairs - Remote USA or Canada at MAPI

        Healthcare Regulatory, Regulatory Affairs. Mapi is adding a Manager, US Regulatory Affairs to our Strategic Regulatory team!...

      2. Quality Assurance Manager - Operations at Siemens

        Division Mobility (MO) Job Type Regular Business Unit Mobility Management Job Time Full-Time Functional Area QA - Quality Assurance/Regulatory Affairs

      3. Director of Regulatory Affairs at Sterling Hoffman Life Sciences

        Create a post-market regulatory project schedule. An appropriate combination of education and regulatory experience i.e. associate degree with 10+ years of...

      4. Director Site Quality Operations at Sanofi Pasteur

        Background in Quality Control, manufacturing and development and/or Regulatory Affairs. Experience interacting with regulatory agencies and health authority...

      5. 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....