Global Medical Devices Regulatory Principal Consultant

ProductLife Group seeks a Principal Consultant in Medical Devices Regulatory Affairs and Quality to lead international regulatory projects in Paris. You will advise on market-access strategies and provide technical expertise across medical devices, IVDs, software, and AI-enabled devices.

You will develop regulatory strategies for Europe, the US, and other markets, lead CE marking and FDA submissions, and ensure robust documentation and risk management. English required; French or Italian a plus.