Senior Regulatory Affairs Lead, MedTech Submissions

Johnson & Johnson in Irvine, CA seeks a Senior Regulatory Affairs Specialist to lead regulatory strategy, submissions, and global registrations for medical devices. You will partner with product teams to ensure timely regulatory milestones and compliance for new and existing products.

Ideal candidates have 6+ years in medical device regulatory affairs, strong communication skills, and experience with FDA and international submissions. Significant travel may be required.