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PMT Corporation, located in Chanhassen, Minnesota, is known for manufacturing and distributing high end, innovative products within the Orthopedic, Neurosurgery, and Plastic Surgery markets. Our workplace is a community of innovators who are passionate about creating an impact. We recognize that the collective power of our team is what propels us forward. Together, we celebrate successes, learn from challenges, and continuously evolve in our pursuit of excellence.
Join us at PMT Corporation if you're ready to be a part of a collaborative, idea-driven, and communicative environment. Your innovation matters, and together, we can continue to shape the future of the medical device industry.
REGULATORY AFFAIRS SPECIALIST OVERVIEW:
The Quality and Regulatory department supports the registration and compliance of PMT Corporation’s products in the U.S. and for over 100 distributors worldwide. The Regulatory Affairs Specialist will focus on assisting with maintaining product compliance with FDA/MDSAP, ISO, and MDD/MDR requirements. We are looking for an excellent communicator and highly organized individual to join our team on-site with an 8:00am – 4:30 pm shift time.
DUTIES AND RESPONSIBILITIES OF THE REGULATORY AFFAIRS SPECIALIST:
QUALIFICATIONS OF THE REGULATORY AFFAIRS SPECIALIST:
PMT is an Equal Opportunity Employment
Location: Chanhassen, MN
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