Join AtomVie Global Radiopharma Inc. as a Batch Release QA Associate and play a key role in the final disposition of radiopharmaceutical products. Your expertise in regulatory compliance will be crucial for maintaining product integrity.

As a QA Associate, you will oversee essential processes such as reviewing documentation, performing media fill reviews, and ensuring adherence to cGMP regulations. This position is critical for the expansion of AtomVie’s operations and aims to make a difference in patients’ lives worldwide.

Key Responsibilities:
• Determine status and deviations of batches
• Participate in drafting and revising operating procedures
• Review Certificates of Analysis and documentation
• Support launch of new products and audits
• Implement corrective actions as needed

Requirements:
• B.Sc or M.Sc in life sciences required
• 3-5 years in a regulated GMP environment
• In-depth knowledge of FDA and Health Canada regulations
• Ability to work in a flexible 24/7 operational environment
• Excellent organizational and cooperative skills

Contribute to high standards of quality assurance at AtomVie as you help enhance healthcare outcomes.
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📌 Batch Release QA Associate Role (Ontario)
🏢 AtomVie Global Radiopharma
📍 Ontario