Found Description
Ensure pharmaceutical quality at AtomVie Global Radiopharma in Hamilton, ON as a Batch Release Quality Assurance Associate. This role focuses on final disposition, documentation reviews, and regulatory compliance.
As a QA Associate, you will oversee the final disposition of batches and verify documentation such as batch records and Certificates of Analysis. Your expertise in GMP compliance will ensure that products meet all necessary specifications, while also participating in standard operating procedures development and internal audits.
Key Responsibilities:
• Review documentation to determine batch status
• Conduct media fill reviews and report discrepancies
• Assist with creation and revision of operating procedures
• Release incoming materials using ERP systems
• Support audits and regulatory inspections
Requirements:
• B.Sc or M.Sc in life sciences with 3-5 years in GMP
• Knowledge of FDA, Health Canada, and EU GMP regulations
• Excellent communic...
As a QA Associate, you will oversee the final disposition of batches and verify documentation such as batch records and Certificates of Analysis. Your expertise in GMP compliance will ensure that products meet all necessary specifications, while also participating in standard operating procedures development and internal audits.
Key Responsibilities:
• Review documentation to determine batch status
• Conduct media fill reviews and report discrepancies
• Assist with creation and revision of operating procedures
• Release incoming materials using ERP systems
• Support audits and regulatory inspections
Requirements:
• B.Sc or M.Sc in life sciences with 3-5 years in GMP
• Knowledge of FDA, Health Canada, and EU GMP regulations
• Excellent communic...
Ready to Apply?
Submit your application for Batch Release Quality Assurance Associate at AtomVie Global Radiopharma Inc.
Apply Now