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Senior Regulatory & QA Lead - Medical Devices; Hybrid
Job Description & How to Apply Below
A healthcare technology firm based in Toronto is seeking a Senior Regulatory Affairs & Quality Assurance Specialist to ensure compliance with regulatory standards and drive quality assurance processes. This full-time hybrid position requires at least 3 years of experience in the medical device industry, familiarity with FDA and ISO regulations, and strong analytical and interpersonal skills. The successful candidate will collaborate with cross-functional teams and be the main point of contact for regulatory agencies.
A comprehensive benefits program and discretionary time off are offered.
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Position Requirements
10+ Years
work experience
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