Make a difference in healthcare as a Quality Assurance Associate at Clarion Medical Technologies. Ensure our medical devices meet the highest quality standards and regulations.

In this role, reporting to the VP of Regulatory Affairs, a Bachelor's degree in Science and 3-5 years of Quality Assurance experience are essential. You’ll be responsible for maintaining compliance with GMP and Health Canada regulations while driving improvements in the Quality Management System (QMS). Your expertise will be key to managing product registrations and supporting quality investigations.

Key Responsibilities:
• Manage batch releases ensuring compliance with regulations
• Enhance and maintain the Quality Management System
• Conduct investigations and handle customer complaints




• Maintain GMP compliance and oversee quality documentation
• Prepare and submit product registrations for health-related items

Requirements:
• Bachelor’s degree in Science or related area
• 3-5 years of experience in regulated QA roles
• Solid understanding of GMP regulations
• Solid problem-solving and analytical skills
• Proficient in documentation and computer systems

Contribute to Clarion Medical Technologies’ mission by ensuring product quality and regulatory adherence.
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📌 Quality Assurance Associate Role at Clarion (Ontario)
🏢 Clarion Medical Technologies
📍 Ontario