Myant is seeking a Quality Engineering Specialist to strengthen manufacturing processes, supplier quality and quality systems within a regulated medical device workplace. The role focuses on quality assurance, process validation, CAPAs and risk management to ensure compliant, high‑quality production.
Ideal candidates will have a solid quality engineering background in medical devices, experience with ISO 13485/EU MDR, and hands-on capability to drive improvements across Manufacturing and
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📌 Medical Device Quality Engineer & Compliance (Ontario)
🏢 Myant
📍 Ontario