Abbott Laboratories in the United States seeks a Principal Regulatory Affairs Specialist to join Abbott’s Vascular Division on-site in St. Paul, MN. The role focuses on global regulatory submissions, ensuring product compliance and timely market approvals.
As an experienced contributor, you will coordinate strategies, prepare filings for FDA and international agencies, and partner with cross-functional teams to support product registrations and post-market activities.
#J-18808-LjbffrGlobal Regulatory Affairs Specialist – Medical Devices in new brighton at Unknown Company
This position is listed as full time and onsite.