Senior Regulatory Affairs Lead – EU Medical Devices

A leading medical device company is seeking a Senior Regulatory Affairs Specialist in Switzerland to provide regulatory support for new product development and ensure compliance with EU regulations. This role requires at least 8 years of experience in regulatory affairs, particularly in the medical device sector. Responsibilities include managing regulatory submissions, collaborating with cross-functional teams, and monitoring changes in regulations. The ideal candidate holds a relevant degree and possesses strong leadership and organizational skills.
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