28.03.24 | Vollzeit | Lausanne | Randstad Schweiz AGMedical Device Directive 93/42/EEC, and Swiss Medical Device Regulation (MedDO). - Familiarity with product EU regulations and directives. - Proficiency in computer literacy, including Microsoft Word, Excel, PowerPoint, and Outlook. - 3-5 years of experience in Medical Device Quality or regulatory
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