3+ years regulatory affairs experience french market
Native french and fluent english communication
IQVIA UK is seeking a Regulatory Affairs Manager for a fixed-term position in France to ensure compliance and manage product lifecycles. The ideal candidate will have over three years of experience in regulatory affairs for medicinal products in the French market and possess excellent communication skills in both French and English
Job Summary
This role involves managing country-level regulatory activities for medicinal products ensuring full compliance with local requirements in France.
The position requires preparing and coordinating regulatory submissions including notifications, renewals, variations, new applications, and MAH transfers.
Candidates will collaborate with leading global pharmaceutical companies to contribute to high-quality regulatory outcomes that make a difference.
Matching Summary
Match Score: 85
IQVIA UK is seeking a Regulatory Affairs Manager for a fixed-term position in France to ensure compliance and manage product lifecycles. The ideal candidate will have over three years of experience in regulatory affairs for medicinal products in the French market and possess excellent communication skills in both French and English.
Skills & Requirements
Must-have
Bachelor of Pharmacy or Life Sciences degree
3+ years regulatory affairs experience French market
Native French and fluent English communication
Knowledge of French pharmaceutical legislation
Experience with regulatory submission preparation
Nice-to-have
Experience in large regulatory organization
Strong organizational skills and attention to detail
Experience with regulatory information systems
Collaborative working style
Experience with artwork tools
Key Requirements
Bachelor of Pharmacy or Life Sciences degree
3+ years experience in regulatory affairs on French market
Native French speaker with fluent English
Excellent knowledge of French pharmaceutical legislation