Regulatory Affairs Project Lead - Medical Devices

Nemera, a global leader in drug delivery systems, seeks a Regulatory Affairs Project Manager based in Lyon. You will lead regulatory and compliance design projects for parenteral and ICO products, coordinating with development and production teams from requirements through to post‑marketing activities.

You will prepare, verify and submit regulatory documents, support QMS development, participate in audits and standardization efforts, and ensure regulatory strategies align with MDR 2017/745, ISO