Elevate healthcare standards with Baxter as a Quality Associate II. Your work will ensure product excellence and regulatory compliance in a supportive team-focused environment.

This position focuses on assisting with quality issues and maintaining high standards through strict adherence to GMP guidelines. You will utilize your expertise to manage non-conformance and support product quality reviews. Team collaboration and effective communication are vital as you work towards enhancing patient outcomes.

Key Responsibilities:
• Ensure adherence to quality standards and procedures
• Provide technical assistance on product quality concerns
• Support quality exception follow-up actions
• Review department procedural changes for compliance
• Manage investigations into quality non-conformance

Requirements:
• University Degree or equivalent in a related field
• Minimum of 3-5 years in quality and manufacturing
• Familiarity with cGMP, ISO, and regulatory standards
• Robust problem-solving and analytical skills
• Intermediate proficiency in MS Office Suite

Your role will significantly impact patient health and product quality at Baxter.
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📌 Baxter Quality Associate II Role (Ontario)
🏢 Socket.dev
📍 Ontario