Catalent is seeking a Quality Assurance Associate in Windsor, Ontario, to ensure compliance and quality in manufacturing processes. Focus on training, documentation, and compliance while working onsite.

This role provides a fantastic opportunity to contribute to quality assurance within the pharmaceutical industry. You will play a vital part in preventing quality issues by reviewing batch documentation and coaching staff on Good Manufacturing Practices (cGMP). Your expertise will ensure products conform to both internal and external quality standards.

Key Responsibilities:
• Perform in-process reviews to guarantee cGMP compliance
• Coach operators on best documentation practices
• Verify equipment and area clearance during changeovers




• Act as a decision-maker for quality issues on shift
• Maintain necessary compliance logs and records

Requirements:
• Bachelor’s degree in related science field
• Experience in a GMP environment preferred
• Solid attention to detail and analytical skills
• Effective verbal and written communication
• Provide credential evaluation for non-Canadian degrees

Join Catalent and leverage your quality assurance skills to drive excellence in pharmaceutical manufacturing.
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📌 Windsor Quality Assurance Associate Role (Ontario)
🏢 Catalent
📍 Ontario