About this opportunity
MicroPort lists this Regulatory Affairs Lead, Medical Devices Global Submissions opportunity in irvine, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
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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Worksite address
irvine, CA, 92713, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.