Catalent is seeking a Quality Assurance Associate to ensure compliance and quality in our recent Adair, ON facility. Engage in critical product audits and training while fostering a culture of continuous improvement.

This position focuses on maintaining high-quality standards in pharmaceutical manufacturing through documentation audits, compliance checks, and coaching. As a vital team member, you will assist in the startup phase, working on final product audits and investigating manufacturing deviations to uphold cGMP standards.

Key Responsibilities:
• Conduct in-process audits and communicate issues promptly
• Perform final release audits for batch documentation
• Investigate manufacturing issues and train staff on cGMP




• Prepare compliance audit reports for management
• Act as quality assurance representative on shift

Requirements:
• Bachelor’s Degree in Science, Engineering, or related field
• Manual dexterity for various tasks
• Strong analytical and problem-solving skills
• Excellent verbal and written communication
• Ability to work independently with minimal supervision

Contribute to Catalent's mission in delivering life-enhancing pharmaceuticals and ensuring excellence on the production floor.
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📌 Quality Assurance Associate at Catalent (Ontario)
🏢 Catalent Pharma Solutions
📍 Ontario