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. 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.
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Global Medical Devices Regulatory Principal Consultant
Il y a 1 jour
Courbevoie, Île-de-France ProductLife Group Temps pleinProductLife 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...
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Global Medical Device Regulatory
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Principal Consultant
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Principal Consultant
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Courbevoie, Île-de-France ProductLife Group Temps plein 110 000 € - 150 000 € ContratMake a meaningful impact on global healthcare — and grow your career while doing it. At ProductLife Group, you’ll join an innovative, forward‑thinking team operating across the world to shape the future of life sciences through expertise, collaboration, and purpose‑driven work.Job DescriptionWe are looking for a Principal Consultant in Medical...