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Global Regulatory Affairs Specialist — Medical Devices; Hybrid
Job Description & How to Apply Below
A leading medical device company in Oakville, Ontario seeks a Regulatory Affairs Specialist for a 12-month hybrid contract. This role involves managing international regulatory submissions and ensuring compliance with medical device regulations, particularly EU MDR. Candidates need a Bachelor's degree and a minimum of 1 year of experience in regulatory affairs. The position offers an annual salary of $55-75K CAD and potential bonuses, contributing to important projects that impact healthcare globally.
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