29.02.24 | Teilzeit | Solothurn | Ypsomed AGOr Natural/Medical Sciences or equivalent experience - At least 4 years of professional experience in Regulatory Affairs with focus medical device - Expertise in Active Medical Devices related regulations and guidance documents in EU and US - Excellent organizational and people skills - Very good English
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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