Regulatory Affairs Specialist — Med Devices

il y a 16 heures


Paris, France Perifit Temps plein

A fast-growing femtech startup in Paris is seeking a Regulatory Affairs Specialist to oversee regulatory and quality activities. You will execute regulatory activities for medical devices, own critical parts of the Quality Management System, and ensure compliance in a fast-paced environment. The ideal candidate has a degree in Engineering or Regulatory Affairs, 3+ years of experience in medical devices, and strong technical writing skills. This role offers an opportunity to make a measurable impact on women's health.
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