Job Description

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100% remote
8 600 – 9 500 zł brutto



Responsibilities:

  • Coordinate medical device and cosmetic regulatory affairs for US and OUS.
  • Coordinate communication internal and external to the regulatory function.
  • Implement regulatory strategies.
  • Support new product introductions and existing product changes.
  • Partner to determine global regulatory strategy.
  • Participate in minimum change documentation.
  • Support risk management files and completion.
  • Support UDI.
  • Review and approve product labelling.



    • Requirements:
  • Bachelor’s degree or higher (completed and verified prior to start) from an accredited institution.
  • 1-2 years of regulatory affairs experience in a private, public, government or military environment.
  • Ability to read, write, and speak English fluently.
  • Fund...

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