AtomVie Global Radiopharma seeks a Quality Assurance Associate for onsite work in Hamilton, ON. This position focuses on ensuring successful batch releases and regulatory compliance.
As a key member of the team, you'll be responsible for reviewing batch documentation and determining the final disposition of radiopharmaceutical products. Your analytical skills will support compliance with strict GMP standards, and you will actively participate in continuous improvement initiatives and support management with data analysis.
Key Responsibilities:
• Ensure accurate documentation for batch final disposition
• Review media fill and participate in operational procedures
• Release incoming materials through ERP systems
• Conduct and support audits and regulatory inspections
• Assist in quality review processes for new product launches
Requirements:
• B.Sc or M.Sc in life sciences with 3-5 years in GMP environments
• Comprehensive knowledge of FDA, Health Canada, a...