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Regulatory Affairs Specialist

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

At Indegene, we're committed to creating a dynamic work environment that fosters growth and development. As a Regulatory Affairs Consultant, you'll play a crucial role in supporting our medical device clients with regulatory expertise.

Key Responsibilities:
  • Provide expert regulatory advice on medical device promotion in France and EU regions
  • Review and approve promotional materials for medical devices in France
  • Develop and implement regulatory strategies for medical device projects
  • Collaborate with cross-functional teams to ensure compliance with regulatory requirements
  • Stay up-to-date with changing regulatory landscapes and provide guidance to the team
Requirements:
  • Life science graduate or post-graduate degree
  • 2-3 years of experience in medical device regulatory affairs, with a strong foundation in device promotion and scientific communication
  • Experience with Germany, EU, and global medical device regulations
  • Strong analytical and problem-solving skills
  • Excellent communication and collaboration skills

We offer a comprehensive benefits package, including medical, regulatory, and editorial review services, as well as operations support from a team of 350+ experienced professionals. If you're passionate about regulatory affairs and want to make a meaningful impact, we encourage you to apply.