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Regulatory Affairs Associate Jr.

Company: Collabera Inc.
Location: Santa Clara
Posted on: November 22, 2021

Job Description:

Job Description

  • 1 to 2 years' experience in a medical device/Pharmaceutical or similarly regulated industry
  • Skills: Ability to schedule and organize multiple projects
  • Education: BS Engineering or Scientific
  • Duties: Manager regulatory submissions to ensure timely regulatory approval of medical devices.--
  • Monitor changing regulations in geographies and translate/communicate these requirements to project development and/or continuous improvement project teams.--
  • Ensure all client product and procedures comply with applicable regulatory agency requirements and guidelines.
  • Experience working on technical files.--

    Skills Required
    Regulatory Affairs Associate ,Regulatory Affairs ,medical device,Pharmaceutical ,regulatory ,medical devices,technical files,MDR,EU MDR

Keywords: Collabera Inc., Santa Clara , Regulatory Affairs Associate Jr., Other , Santa Clara, California

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