Make a difference at Abbott as a Senior Associate in Quality Assurance. This in office role offers a chance to ensure compliance with critical regulations while fostering health improvement initiatives.
Located in Mississauga, Ontario, this position requires four days on-site with one remote day. You will focus on upholding ISO 13485 and Canadian Medical Device Regulations (CMDR). Your expertise in quality compliance will play an integral role in enhancing Abbott's diagnostic technologies and overall health management.
Key Responsibilities:
• Ensure compliance with ISO 13485 and CMDR regulations
• Facilitate site audits and support manufacturer audits
• Interact with Health Canada for Food & Drugs Act compliance
• Conduct annual internal audits for quality assurance
• Oversee documentation change management processes
Requirements:
• Bachelor's degree in a scientific or technical field
• 3-5 years in Quality Assurance within a regulated industry
• Knowledge of Quality Systems and Regulatory Science
• Experience with ISO audits and CMDR
• Preferred background in Compliance or Regulatory Affairs
Leverage your quality assurance skills to enhance health outcomes at Abbott in Mississauga.
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