Exquisite Biomedical Consulting is seeking a Regulatory Affairs Associate to support regulatory strategy, submissions, and lifecycle documentation for medical devices and related life sciences products across Health Canada, US FDA, and EU MDR. You'll turn regulatory requirements into actionable plans and coordinate input from clinical, quality, and engineering teams.
You will report to the CEO and engage with diverse clients, managing deadlines and ensuring records are accurate.
📌 Regulatory Affairs Lead Medical Devices Submissions Vancouver
🏢 Exquisite Biomedical Consulting
📍 Vancouver
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