Regulatory Affairs Junior (Medical Device)

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Full Remote
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Offer summary

Qualifications:

Bachelor's degree in life sciences or related field., Strong understanding of regulatory requirements for medical devices., Excellent communication and organizational skills., Ability to work collaboratively in a team environment..

Key responsibilities:

  • Assist in the preparation and submission of regulatory documents.
  • Support the regulatory team in maintaining compliance with regulations.
  • Conduct research on regulatory guidelines and standards.
  • Participate in meetings with cross-functional teams to ensure alignment on regulatory strategies.

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QUALIPHARMA
51 - 200 Employees
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