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 Good 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
• Robust 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 (Ontario)
🏢 Catalent
📍 Ontario