Join Clarion Medical Technologies as a Quality Assurance Associate, focusing on patient safety through regulatory compliance and quality control. Contribute to innovative healthcare solutions in Canada.

Reporting directly to the VP of Regulatory Affairs, this role requires a Bachelor’s degree in Science and 3-5 years of experience in Quality Assurance. You'll ensure products comply with GMP and Health Canada standards while enhancing the Quality Management System (QMS). Your role will be crucial in managing quality investigations, product registrations, and continuous improvement processes.

Key Responsibilities:
• Ensure compliance with GMP during batch releases
• Drive continuous improvement of the QMS and eQMS
• Oversee customer complaints, CAPAs, and quarantined inventory




• Conduct supplier reviews and maintain quality documentation
• Prepare registrations for various healthcare products

Requirements:
• Bachelor's degree in Science or a related discipline
• 3-5 years of relevant Quality Assurance experience
• In-depth knowledge of GMP and regulatory compliance
• Robust analytical and investigation skills
• Proficiency in managing documentation and computer systems

Support Clarion in delivering top-tier medical technologies with your expertise in quality assurance.
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📌 Clarion Quality Assurance Specialist (Ontario)
🏢 Clarion Medical Technologies
📍 Ontario