eBay Classifieds » All ads » Jobs » 

regulatory affairs in Greensboro

(1-2 of 2 ads)
View as:
Categories
  1. 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...

  2. 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...

  3. 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:....

  4. 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...

  5. Medical Writer I at Planet Pharma

    Medical writing, regulatory affairs, clinical research, engineering). Ph.D/Pharm D plus 1 to 2 years of related medical device/drug industry experience (e.g....

    Ads
    1. Academic Program Director - Family Nurse Practitioner Program

      Location: High Point, North Carolina Faculty: Full Time Education: Professional Doctorate Degree Required Experience: Teaching & Academic leadership Requirement: Local to Greensboro / High Point Area Job Summary: The Program Director is a member of the faculty (rank commensurate with experience) who also holds an administrative appointment related to managing a specific program or programs ...

    2. Regulatory Support

      Adecco Engineering and Technology is currently assisting a local client in need of a Regulatory Support Specialist located inGreensboro,NC. This will be an on-going contract job opportunity. The main responsibility of this role is to provide regulatory expertise and support to enable business growth, compliance, customer value and competitive position. Other duties will include but are not ...

      1. Quality Manager, Instrument Manufacturing at Becton Dickinson & Company

        Qualifications Bachelor of Science ( BSc) or Engineering (B.Eng.), Master and/or specialization in regulatory affairs and good knowledge of molecular biology is...

      2. 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....

      3. 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...

      4. 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),...

      5. 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...