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regulatory affairs in Raleigh

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  1. Medical Science Liaison, Sleep (Midwest or Southeast) at Jazz Pharmaceuticals

    Thorough understanding of applicable federal and state regulatory requirements for field-based scientific personnel....

  2. Senior Medical Science Liaison, Sleep (Ohio Valley) at Jazz Pharmaceuticals

    Thorough understanding of applicable federal and state regulatory requirements for field-based scientific personnel....

  3. Vice President of Integrated Delivery System Strategy at Cigna

    Coordinate with the compliance team members responsible for interacting with Cigna Legal and Governmental affairs....

  4. STATISTICIAN - CANCER CENTER WHELAN RESEARCH - MSW at Mount Sinai Health System

    Regulatory affairs of the IRB. Meets regulatory, licensure and annual health. Mount Sinai Health System Careers....

  5. IT Lead, Regulatory Affairs Business Analyst R&D at Johnson & Johnson Medical NV

    We are looking for an IT leader that, with oversight from the IT Regulatory Affairs Product Line Organization, will partner with the R&D Regulatory Affairs...

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    1. Live-in Caregiver for Quadriplegic woman in Wheelchair

      I am a C6 quadriplegic (paralyzed from the chest down) from a spinal cord injury. I live in Raleigh, North Carolina (Cameron Village). I am in search of a full-time live in caregiver 3 days/3 nights a week (Sunday 8 p.m. – Wed 8 p.m.) . Please apply only if you are looking for a long-term position and steady employment. PAY: $140-$160 DAY plus free room, Internet & TV with food share, Room & Board PLEASE SEND PHOTO Responsibilities include: • Transfer from bed to wheelchair, shower chair etc. • Bathing & Bowel program • Catheter care • Dressing, make-up, hair • housekeeping • Meal ...

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      No Internship
      Freelance Allowed
      No Telecommute

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    1. Drug Delivery Medical Devices Regulatory Affairs Specialist

      Seeking track record in oversight of regulatory submissions for the US, EU and ROW registrations and Quality System compliance processes such as CAPA, change orders, internal audits and adverse issues. Requires 4+ years of experience in Medical Device Regulatory Affairs for an ISO 13485 environment. Activities: *** Preparing and filing regulatory submissions including registration of ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Clinical SAS Programming Lead at MMS Holdings Inc.

      Our core service areas include medical and regulatory writing, biostatistics, clinical programming, data management, clinical development, clinical trial...

    1. Medical Devices Sr. Regulatory Affairs Associate - Raleigh, NC

      Seeking experience supporting compliance with domestic and international regulatory requirements for drug administration-delivery medical devices such as: prefilled syringes, inhalers or similar. Shall: *** Interface with FDA, Notified Body, and other external regulatory representatives relating to: Audits, Vigilance, Medical Device Reporting, 510(k) filings, license renewals, ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Senior Biostatistician - Remote at MMS Holdings Inc.

      We are a pharmaceutical service provider supporting pharmaceutical and biotech industries with medical writing, biostatistics, clinical programming, data...

    1. Regulatory Affairs & Quality Specialist - Medical Devices - Durham, NC

      Seeking Regulatory Affairs and Quality System expertise in Medical Device manufacturing and a track record supporting and improving a quality and results driven company culture with excellent regulatory compliance and continually improving operations to support and coordinate registration, device licensing, surveillance, adverse event and corrective action reporting, translation, product ...

      No PartTime
      No Contract
      No Internship
      No Freelance
      No Telecommute

    1. Senior Clinical Data Manager - Remote at MMS Holdings Inc.

      Our core service areas include medical and regulatory writing, biostatistics, clinical programming, data management, clinical development, clinical trial...

    1. Project Specialist at Premier Research

      Assisting in overall Project Delivery through coordination of efforts assigned to entire project team, (including Regulatory, Clinical Operations, Biometrics,...

    1. Sr. Director QA at Teleflex

      Perform other duties assigned by the Global Vice President Regulatory Affairs & Quality Assurance. Provides expert opinion, advice and recommendations to the...

    1. Quality Assurance/Regulatory Affairs Project Lead at Teleflex

      A minimum of 5 years regulatory affairs, compliance, or quality assurance experience. Assist Teleflex’s Regulatory Affairs and Quality Assurance department...

    1. Quality Engineer at Teleflex

      Interface with various internal and external resources such as Manufacturing Product Development, marketing, and Regulatory Affairs to assist with obtaining...

    1. Quality Assurance Specialist at Konica Minolta Medical Imaging

      Advises management on regulatory changes and provides impact analysis. Bachelor’s Degree in related technical field preferred, and 5-7 years experience in...

    1. Clinical Research Associate/Lead Clinical Research Associate at Merz North America, Inc.

      Provides visit feedback for evaluation by the Clinical Affairs group/or designee. Witness first dosing on studies and report back to clinical affairs team if...

    1. Regulatory Affairs Consultant (QE) at Black Diamond Networks

      Join a team of senior regulatory affairs professionals to assist medical device manufacturer in push to deliver multiple regulatory filings....

      1. Clinical Quality Assurance Professional at W. L. Gore & Associates

        Participating in Clinical Affairs Process Improvement initiatives. Serving as a primary contact for regulatory inspections....

      2. Senior Clinical Research Operations Specialist at Chiltern International

        Interface with Regulatory Affairs to obtain regulatory document approval for clinical study sites; Coordinate site regulatory document collection for assigned...

      3. Product Monitoring Specialist (Men/Women) based in Saint louis at Guerbet

        Work in conjunction and effectively communicate with cvarious departments, including legal Affairs, Regulatory Affairs, R&D, Marketing, Medical Affairs, Sales...

      4. LIMS SME/Business Analyst at LabAnswer

        The LIMS SME/Business Analyst will provide support for an enterprise StarLIMS implementation for the Food and Drug Administration (FDA) Office of Regulatory...

      5. Medical Science Liaison, Infectious Disease- NC, OH, WV, KY at Janssen Scientific Affairs, LLC

        Janssen Scientific Affairs, LLC (6120). Janssen Scientific Affairs, LLC, a Johnson and Johnson Company, is recruiting for a Medical Science Liaison (MSL) -...