Regulatory Affairs & Quality Specialist – Benelux & France

MiniMed seeks a Regulatory Affairs & Quality Specialist to support regulatory and quality activities across Benelux and France, ensuring EU and local compliance throughout the product lifecycle. The role involves working with Competent Authorities, customers, tenders and internal stakeholders, and requires two days a week at one of our offices in Paris, Maastricht, Heerlen or Eindhoven.

You will manage FSCA actions, post‑market surveillance, and the alignment of local regulatory requirements