Remote EU MDR Regulatory Lead - Class I Devices

elemed is seeking a regulatory lead for its Class I medical device portfolio under the EU MDR. The role involves owning technical documentation, labeling, UDI and EUDAMED, and ensuring proper assessment of product changes before launch.

You will drive ongoing compliance, tighten processes, and improve templates to simplify regulatory work across quality, R&D, operations and marketing. Remote in France with occasional travel and independent stakeholder management are required.