MiniMed seeks a Regulatory Affairs professional to craft global clinical regulatory strategies for next-generation diabetes devices, including FDA submissions and EU MDR compliance. You will collaborate with clinical, R&D, and quality teams in a matrixed environment to ensure timely regulatory approvals.
Role emphasizes global regulatory intelligence, submission management, and liaison with regulators. Requires experience with PMAs/510(k) and international submissions, with full remote work
#J-18808-LjbffrRemote Global Regulatory Affairs Lead – Medical Devices in california at Unknown Company
This position is listed as full time and able to be worked remotely.