Global Regulatory Affairs Lead – Drug & Device

A leading precision medicine company in San Diego, CA, seeks an Associate Director of Regulatory Affairs to develop and implement regulatory strategies for drug and device submissions. This role involves guiding cross-functional teams, interacting with health authorities, and ensuring timely submissions. Candidates should have a Bachelor's degree, ideally a PhD/PharmD, and 8+ years of experience in Regulatory Affairs, preferably with biologics or drug/device products. A hands-on leader with strong communication skills is essential. #J-18808-Ljbffr