Quality Engineer for Medical Devices
Job in
Toronto, Ontario, C6A, Canada
Listed on 2026-08-03
Listing for:
Proximate Technologies Inc
Full Time
position Listed on 2026-08-03
Job specializations:
-
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist -
Engineering
Quality Engineering, Biomedical Engineer, Regulatory Compliance Specialist
Job Description & How to Apply Below
Your role will focus on the Quality Management System and continuous improvement initiatives.
We are seeking a skilled Quality Engineer with a Bachelor's degree in Engineering and over three years of experience in the medical device field. You will maintain and improve our Quality Management System (QMS) while supporting compliance with ISO 13485, FDA regulations, and GMP standards. Collaboration with various teams will enhance product quality and streamline processes.
Key Responsibilities:
• Maintain and enhance the Quality Management System (QMS)
• Support CAPA, complaint investigations, and root cause analysis
• Ensure compliance with ISO 13485 and FDA regulations
• Assist in process validation and risk management activities
• Collaborate for better product quality and support audits
Requirements:
• Bachelor's degree in Engineering or related field
• Minimum 3 years of Quality Engineering experience
• Knowledge of FDA Quality System Regulations
• Strong problem-solving abilities
• Excellent communication skills
Elevate product quality and drive compliance in the medical device sector as a Quality Engineer.
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