Regulatory Affairs Lead, Medical Devices Global Submissions

A leading medical device company in Irvine, CA is seeking a Project Manager for Vertical Marketing and Regulatory Affairs. The role involves managing regulatory compliance processes, leading global submissions, and overseeing project operations. Candidates should have 5-8 years of regulatory experience in the medical device industry, preferably with supervisory experience. Excellent benefits, including competitive insurance and a 401K plan, are offered.
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