Regulatory Affairs Lead: Medical Devices & FDA Submissions

A medical device company in Menlo Park seeks a Regulatory Affairs Manager. The role involves providing regulatory guidance for R&D teams, preparing FDA submissions, and ensuring compliance with medical device regulations. The ideal candidate has over 5 years of experience in the medical device industry and a proven track record of submitting 510(k)s and IDE submissions. This full-time position offers opportunities to work in a dynamic environment focusing on vascular solutions. #J-18808-Ljbffr