Hybrid Reg Affairs & Quality Specialist - EU Med Devices

MiniMed is looking for a Regulatory Affairs & Quality Specialist in Paris to support compliance with EU and local regulations throughout the product lifecycle. In this hybrid role, you'll engage with regulators and internal teams, ensuring quality procedures align with regulations.

The ideal candidate should possess 3–5 years of medical device experience, communication skills in French and English, and advanced skills in Microsoft Office. Join MiniMed and enjoy a competitive salary and flexible benefits package.