Regulatory Affairs Manager

IQVIA

Manage country-level regulatory activities
Prepare and coordinate regulatory submissions
Lead submission processes with health authorities
As a Regulatory Affairs Manager, you will play a key role in ensuring compliance and supporting successful product lifecycle management in France

Job Summary

  • As a Regulatory Affairs Manager, you will play a key role in ensuring compliance and supporting successful product lifecycle management in France.
  • You’ll collaborate with leading global pharmaceutical companies and contribute to high‑quality regulatory outcomes that truly make a difference.
  • When you join IQVIA, you become part of a global team that is dedicated to driving smarter healthcare for everyone, everywhere.

Matching Summary

As a Regulatory Affairs Manager, you will play a key role in ensuring compliance and supporting successful product lifecycle management in France.

Skills & Requirements

Must-have

  • Manage country-level regulatory activities
  • Prepare and coordinate regulatory submissions
  • Lead submission processes with Health Authorities
  • Prepare and translate product labelling
  • Monitor local pharmaceutical legislation

Nice-to-have

  • Collaborate with industry experts
  • Foster a culture of innovation
  • Contribute to meaningful work
  • Experience within a large regulatory organization

Key Requirements

  • 3+ years of experience in regulatory affairs
  • Bachelor of Pharmacy or Life Sciences degree
  • Native French and fluent English communication skills
  • Excellent knowledge of French pharmaceutical legislation

Work Rights

Not specified

Tailored Resume

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