08.03.24 | Vollzeit | careers.tecan.comLeading and organizing Task Forces resulting from investigations to initiate or accompany short-term corrective actions. - Assessing deviations regarding reporting obligations in cooperation with the Global Complaint Unit and Regulatory Affairs based on investigation results. - Implementing the Quality
Später ansehen31.10.19 | Vollzeit | Bern | DecomplixYou bring - a technical background and enjoy writing technical documents; - professional experience in quality management or regulatory affairs in the Medtech industry; - detailed knowledge of ISO 13485 and the certification processes for medical devices in Europe, ideally for software-only products
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