Senior Regulatory Affairs Lead – Med Device FDA Submissions
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Senior Manager Regulatory Affairs
Il y a 3 jours
Les Ulis, Île-de-France elemed Temps plein 70 000 € - 110 000 € ContratSenior Regulatory Affairs Consultant The Company: If you are a QA/RA professional with an interest in innovation and groundbreaking development, we have an incredible role for you. This is a chance to join an established midsize Software as a Medical Device company. Role Responsibilities & Qualifications: Develop and execute regulatory strategies/plans that...
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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...
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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 5 jours
Issy-les-Moulineaux, Île-de-France Withings Temps pleinDescriptionAbout 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...
