Regulatory Affairs & Quality Specialist (Benelux/France)

MiniMed in Paris is seeking a Regulatory Affairs & Quality Specialist to support regulatory and quality activities across Benelux and France, ensuring EU and local compliance throughout the product lifecycle. You’ll collaborate with authorities, customers and internal teams in a dynamic international environment.

This hybrid role requires presence two days per week in Paris or other offices; 3–5 years in medical device regulatory/quality and fluent French and English are expected, with strong