Advance your career with AtomVie Global Radiopharma Inc. as a Quality Assurance Associate specializing in batch release. This pivotal role ensures compliance and quality of vital radiopharmaceutical products in a GMP setting.

In this position, you will manage documentation reviews, support regulatory compliance, and ensure all materials meet the required specifications. The QA Associate role is essential for maintaining AtomVie’s commitment to transforming healthcare positively.

Key Responsibilities:
• Review required documentation for batch disposition
• Conduct media fill reviews and report findings
• Aid in creating standard operating procedures
• Assist in annual product reviews and audits
• Maintain thorough records to meet compliance

Requirements:
• B.Sc or M.Sc in life sciences strongly preferred
• 3-5 years experience in GMP or regulated environments
• Familiarity with Health Canada, FDA, and EU GMP
• Capable of supporting a flexible shift schedule
• Solid detail orientation and communication skills

Join AtomVie in delivering high-quality radiopharmaceuticals that change lives and adhere to the rigorous standards of the healthcare industry.
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📌 Quality Assurance Associate in Radiopharma (Ontario)
🏢 AtomVie Global Radiopharma
📍 Ontario