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  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....

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    1. Sr. Manager Regulatory Affairs-CMC

      Sr. Manager Regulatory Affairs-CMC Needed for a well funded US Biopharmaceutical Company · Global Regulatory Affairs Strategy · Clinical Development · Phase II-III · Oncology· Immunology · Neurology  Manager/Sr. Manager Level | Regulatory Affairs | CMC/Small MoleculeLocation: SeattleSalary: $130,000-$170,000 + bonus + excellent benefits This biopharmaceutical company set in the beautiful ...

    2. Clinical Research Associate - West Coast Region - Home-Based

      ~~We are currently looking for a knowledgeable, entrepreneurial and innovative person to join our Clinical Operations team in the West Coast Region.   If you are eager to work on full-scale complex trails within multiple therapeutic areas, provide us with expertise and guidance in the region, help strengthen our local presence and be involved in something new, outstanding and challenging, ...

    3. Sr. Manager Regulatory Affairs-CMC

        Sr. Manager Regulatory Affairs-CMC Needed for a well funded US Biopharmaceutical Company Global Regulatory Affairs Strategy Clinical Development Phase II-III Oncology Immunology Neurology   Manager/Sr. Manager Level | Regulatory Affairs | CMC/Small Molecule Location: Seattle Salary: $130,000-$170,000 + bonus + excellent benefits   This biopharmaceutical company set in ...

    4. Manager Direct Import: Compliance Operations (Seattle, Washington)

        Manager Direct Import: Compliance Operations (Seattle, Washington) Talent Orchard is seeking Manager Direct Import: Compliance Operations who is a customer-focused Program Manager- Operations to lead the vendor and customer escalations team within our Product Compliance team. The Manager of the Product Compliance Operations team is expected to become a subject matter expert and support ...

    5. Sr Manager, Engineering Development

      Sr Manager, Engineering Development Description The Senior Development Manager provides leadership, expertise, communications, quality control, and guidance for National Development projects as well as direct oversight of the Real Estate, Zoning and Construction and Special Project teams. The role provides value to the Development function by ensuring consistent high quality and timeliness ...

    6. Manager Direct Import: Compliance Operations (Seattle, Washington)

        ~~Manager Direct Import: Compliance Operations (Seattle, Washington) Talent Orchard is seeking Manager Direct Import: Compliance Operations who is a customer-focused Program Manager- Operations to lead the vendor and customer escalations team within our Product Compliance team. The Manager of the Product Compliance Operations team is expected to become a subject matter expert and ...

    7. Director, QA & Regulatory - immediate hire

      The Director, QA & Regulatory will:      * Manage the Quality Assurance, Quality Control and Regulatory functions for the organization      * Ensure compliance with pertinent regulations, standards, and clinical practice guidelines      * Oversee the content, production, assembly and administration of regulatory submissions      * Foster a culture of excellence, professional integrity and ...

    8. Clinical Research Associate - West Coast Region - Home-Based

      ~~We are currently looking for a knowledgeable, entrepreneurial and innovative person to join our Clinical Operations team in the West Coast Region.   If you are eager to work on full-scale complex trails within multiple therapeutic areas, provide us with expertise and guidance in the region, help strengthen our local presence and be involved in something new, outstanding and challenging, ...

      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...