Strategic Regulatory Affairs Lead — Medical Devices

Bracco Medical Technologies is seeking a Principal Regulatory Affairs Specialist to develop and execute regulatory strategies for medical device products across lifecycle changes. You’ll lead global submissions and provide on‑site regulatory support for 510(k), EU MDR, and Health Canada efforts. You will collaborate with cross‑functional teams, mentor staff, and oversee regulatory documentation, labeling review, and agency communications to ensure ongoing compliance and market access.