Global Regulatory Affairs Lead (Medical Devices) — Remote

MiniMed is seeking a Regulatory Affairs professional to shape global clinical regulatory strategies for next‑generation diabetes devices, reimbursement, and post‑market surveillance. You will partner with clinical, medical affairs, and engineering in a matrixed environment across US, EU, and other regions. You will prepare FDA PMAs/510(k), EU MDR filings, and technical dossiers, maintain regulatory intelligence, and drive lifecycle changes while ensuring QMS compliance. #J-18808-Ljbffr MiniMed Group