Regulatory Affairs & Quality Specialist — Europe (Hybrid, Paris/Benelux)

MiniMed seeks a Regulatory Affairs & Quality Specialist to support regulatory and quality activities across Benelux and France, ensuring EU/local compliance throughout the product lifecycle. You will liaise with authorities, customers, and internal stakeholders, guiding regulatory processes and post-market activities.

This hybrid role requires two days per week in Paris or other offices. Responsibilities include FSCA preparation, evidence gathering, post-market surveillance support, and