Medical Products Coordinator

5 days ago


Solna Municipality, Sweden TN Sweden Full time
Job Description

This position reports to the Regulatory Affairs Manager and is based at our office. We apologize for any delay in responding to your application during the summer holiday season.

Key Responsibilities
  1. Coordinates compilation and submission of new drug applications, cosmetics, medical devices, food supplements or similar products.
  2. Collects and organizes information on regulatory requirements for quality, preclinical and clinical data.
  3. Prepares and submits regulatory submissions according to applicable regulations.
  4. Monitors progress of regulatory authority review process.
  5. Prioritizes projects against defined timelines.
  6. Maintains thorough understanding of regulatory environment and supporting data requirements.


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