Global Medical Devices Regulatory Principal Consultant
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ProductLife Group seeks a Principal Consultant in Medical Devices Regulatory Affairs and Quality to lead international regulatory projects in Paris.
Les qualifications, les compétences et toute l'expérience pertinente nécessaires pour ce poste se trouvent dans la description complète ci-dessous.
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. xuezdbg
English required; French or Italian a plus.
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