Medtronic Canada is seeking a dedicated regulatory affairs contributor for a 6-month contract to coordinate document packages for regulatory submissions, audits, and inspections. You will lead submission materials, renewals, and registrations while driving compliance across labeling, manufacturing, and clinical protocols.
The role requires a Baccalaureate degree with 2+ years of relevant experience, or an advanced degree with minimal experience.
📌 Regulatory Affairs Specialist — Health Canada Submissions (Winnipeg)
🏢 CAN Medtronic Canada ULC
📍 Winnipeg
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