Regulatory Affairs Specialist

il y a 1 jour


Paris, Île-de-France Indegene Temps plein
Regulatory Affairs Consultant

Indegene is seeking a highly skilled Regulatory Affairs Consultant to join our team. As a key member of our regulatory team, you will be responsible for providing expert regulatory advice on medical device promotion and scientific communication materials in France and other regions.

Key Responsibilities:

  • Provide guidance on standards pertaining to advertising and promotion of medical devices in France and the EU.
  • Review and approve medical device promotional and non-promotional materials for compliance with French regulatory requirements.
  • Collaborate with our material review team to ensure client project requirements are met.
  • Provide strategic input on regulatory affairs matters, including understanding the collaboration between global and local markets for medical device promotional materials.

Requirements:

  • Life science graduate or post-graduate with a strong foundation in medical device regulatory affairs.
  • 2-3 years of experience in review and approval of medical device promotional and non-promotional materials.
  • Experience with German, EU, and global medical device regulations.

What We Offer:

  • A comprehensive medical, regulatory, and editorial review services team.
  • Opportunities for growth and development as a regulatory affairs professional.

How to Apply:

Please upload your CV in English to apply for this exciting opportunity.


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