Onsite Quality Assurance Associate

Position: Onsite Quality Assurance Associate Opportunity
Atom Vie 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, and EU guidelines

• Strong organization and independent working abilities

• Flexibility for shift work in production

• Excellent communication skills for collaboration

Leverage your quality assurance expertise at Atom Vie to enhance regulatory compliance and product integrity.
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