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 setting - 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