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 will collaborate with leading global pharmaceutical companies and contribute to high-quality regulatory outcomes that truly make a difference.
IQVIA fosters a culture of innovation, teamwork, and shared purpose, offering opportunities to grow your regulatory career through continuous learning.
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
Regulatory submissions coordination
Compliance with French pharmaceutical legislation
Product lifecycle management
Regulatory document preparation
Collaboration with Health Authorities
Nice-to-have
Experience with regulatory information systems
Artwork and promotional material review
Collaborative working style
Strong organizational skills
Continuous learning culture
Key Requirements
Bachelor of Pharmacy or Life Sciences degree
3+ years regulatory affairs experience in French market
Native French and fluent English communication skills