Director, CQRA: Regulatory, Quality & Clinical

A leading medical device company in Lainate, Italy is seeking a Director of Clinical, Quality, and Regulatory Affairs to oversee compliance with EU MDR and FDA standards. This pivotal role involves leading CQRA functions, ensuring effective regulatory submissions, and integrating quality assurance across product development. The ideal candidate will hold a degree in Engineering or Life Sciences with 7 to 10 years of relevant experience. Strong leadership and communication skills are essential. This position supports the organization's quality-driven culture.
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