Contribute to top-tier product integrity as a Quality Associate II at Baxter. Ensure compliance with regulations and maintain high quality standards within a dynamic team workplace.

In this role, you will provide day-to-day support on product quality issues and ensure adherence to GMP and regulatory standards. As a key member of our Quality team, you will help investigate non-conformance events and provide technical assistance on procedural changes. Your expertise will be critical in maintaining operations that directly impact patient care.

Key Responsibilities:
• Address product quality issues ensuring compliance with GMP
• Support plant operations including overtime and shutdowns




• Review and approve procedural changes and product concerns
• Facilitate timely follow-ups on quality exceptions
• Initiate investigations for non-conformance events

Requirements:
• University Degree or equivalent experience
• 3-5 years in manufacturing and quality roles
• Knowledge of cGMP and regulatory standards
• Strong communication and analytical skills
• Proficiency in MS Office Suite

Your ability to ensure quality and compliance will be essential to Baxter’s mission in healthcare.
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📌 Quality Associate II at Baxter (Ontario)
🏢 Socket.dev
📍 Ontario