Regulatory and Clinical Affairs Specialist at Withings

Withings is hiring a hybrid Regulatory and Clinical Affairs Specialist to support the evaluation of medical devices, obtain and maintain market authorizations, and maintain clinical and post-market documentation. The role covers scientific and regulatory monitoring, risk analysis, regulatory strategy, technical and registration dossiers, interactions with notified bodies and authorities, and post-market surveillance. Candidates need a scientific, biomedical, engineering, or equivalent Bac+5 qualification, prior experience in medical-device regulatory or clinical affairs, knowledge of EU MDR and related standards, strong writing and analytical skills, and fluency in French and English.