Remote Regulatory Affairs Specialist, Medical Devices EU MDR
Location: Germany
A leading medical device consultancy is seeking a Regulatory Affairs Specialist to ensure compliance for a reputed company of medical devices in Europe and Switzerland. The role involves maintaining regulatory documentation, preparing technical files, and supporting post-market activities. Key skills required include experience in regulatory affairs, knowledge of EU MDR, reputed company in German, and the ability to work cross-functionally. This is a permanent remote position with occasional travel needed.
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