Global Regulatory Affairs Specialist - Medical Devices
Laborie
Laborie is seeking a Regulatory Affairs Specialist to join our team in a hybrid role based out of Minnetonka, MN or Portsmouth, NH. You will support global product registration, approvals, and lifecycle management across major markets including the US, Canada, Europe, and other regions. The role involves preparing submissions, maintaining regulatory documents, and ensuring ongoing compliance with global requirements in collaboration with cross-functional teams. #J-18808-Ljbffr Laborie
Vacancy posted 9 hours ago
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