Global Regulatory Affairs Specialist - Medical Devices
Scanlan International, Inc.
Scanlan International, Inc. is a medical device company seeking a Regulatory Affairs Specialist to maintain market authorizations and oversee regulatory documentation for worldwide markets. The role is based at the headquarters south of downtown St. Paul with an on-site work environment Monday through Friday. Responsibilities include FDA/Canada/EU registrations, post-market surveillance, CAPA investigations, and regulatory records management. #J-18808-Ljbffr
Vacancy posted 4 days ago
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