Bracco Medical Technologies in Eden Prairie, MN is seeking a Principal Regulatory Affairs Specialist to develop and execute regulatory strategies for medical device products across global markets.
You will lead cross-functional teams, manage FDA submissions (510(k)), EU MDR/CE marking, Health Canada filings, and maintain compliance, labeling, and lifecycle changes. 7+ years experience required.
#J-18808-LjbffrGlobal Regulatory Strategy Lead, Medical Devices in northern at Unknown Company
This position is listed as full time and onsite.