Clinical & Regulatory PM: FDA/CE Submissions

Withings in Issy-les-Moulineaux is seeking a technical project manager to organize regulatory and clinical work. You will plan, track, and drive FDA and CE submissions in collaboration with the Chief Clinical & Regulatory Affairs Officer, owning the execution plan and follow-through.

You will coordinate across Regulatory, QMS, Clinical Operations, Medical Data Sciences, and product/legal teams, ensuring timely deliverables and effective use of AI tools with human verification.