Elevate your career with Catalent as a Quality Assurance Associate in Windsor, Ontario. Focus on quality compliance, documentation training, and continuous improvement in a fully onsite role.

This position offers a unique opportunity to create a culture of quality and compliance in a pharmaceutical manufacturing environment. As a Quality Assurance Associate, you will implement Valuable Manufacturing Practice (cGMP) requirements, coach operators on documentation standards, and facilitate in-process batch reviews. Your insights will directly contribute to product integrity and help prevent quality issues from arising.

Key Responsibilities:



• Review documentation for compliance with cGMPs and SOPs • Assist in managing manufacturing events and deviations • Verify line clearance during product changeovers • Act as Quality Assurance representative for your shift • Monitor GMP compliance for inspection readiness

Requirements: • Bachelor’s degree in science; Chemistry preferred • Experience in a GMP or pharmaceutical environment • Strong analytical and communication skills • Detail-oriented with manual dexterity • Eligible for non-Canadian credential evaluation

Bring your expertise and attention to detail to Catalent, ensuring product quality every step of the way. #J-18808-Ljbffr

📌 Quality Assurance Associate in Windsor (Winnipeg)
🏢 Catalent
📍 Winnipeg