Regulatory-Tech PM for FDA/CE Submissions
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Withings is seeking a Technical Project Manager for Clinical & Regulatory Affairs in Issy-les-Moulineaux, France. You will plan, track and drive FDA and CE submissions, regulatory monitoring and data verification, collaborating with the Chief Clinical & Regulatory Affairs Officer to move complex processes forward.
Ideal candidates have 3–6 years in project management, strong stakeholder skills, and a quantitative technical background.
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Clinical & Regulatory PM: FDA/CE Submissions
Il y a 1 jour
Issy-les-Moulineaux, Île-de-France Withings Temps plein 70 000 € - 100 000 € ContratWithings 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...
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Technical Project Manager, Clinical
Il y a 4 jours
Issy-les-Moulineaux, Île-de-France SportsTechJobs Télétravail Temps plein 70 000 € - 100 000 € Contrat# Withings is hiring a Technical Project Manager, Clinical & Regulatory Affairs## Get the latest jobs to your inbox!1. Home2. /3. Jobs at Withings4. /5. Technical Project Manager, Clinical & Regulatory AffairsIssy-les-Moulineaux, FrancePosted 2 days ago21 viewsUnlock Premium - Save Jobs, Set Alerts & Get Early Access### Job Description**About...
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Technical Project Manager, Clinical
Il y a 1 jour
Issy-les-Moulineaux, Île-de-France Withings Temps plein 70 000 € - 100 000 € ContratAbout Withings: Withings designs connected health devices (scales, blood pressure monitors, ECG watches, an under-mattress sleep sensor) and AI-based medical software (SaMD) used every day by millions of people. Our Medical Department runs several FDA 510(k) submissions, CE certification under the EU MDR, and clinical studies in France and the US in...
