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regulatory affairs in Louisville

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  1. Fuels Trader at Exelon Corporation

    This person will work closely with other members of the Fuels Team, regional power desks, plant operations, portfolio planning, risk management, key suppliers,...

  2. 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!...

  3. Project Assistant - IVRS (Interactive Voice Reposnse System) at Worldwide Clinical Trials

    Project Assistant, Junior Project Manager, IVRS PM, Technical Project Manager, Regulatory Affairs Coordinator, IVRS Development Manager, IVRS Development...

  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. 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. 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. Pharmacuetical Lab Consultant at Avarent LLC

        Our experience in Pharmaceuticals, Medical Devices and Biologics extends from Regulatory Affairs and Quality Assurance to Process Engineering....

      4. Contract eCTD Submissions Manager at Clinipace Worldwide

        Regulatory Affairs Certificate a plus. Minimum of eight (8) years relevant publishing experience, preferably in Pharmaceutical Regulatory Affairs....

      5. Project Manager for Product Development (Kansas City) at RBC Medical Innovations

        Development, Manufacturing, Purchasing, Quality and Regulatory Affairs, and. Project Manager for Product Development....