Elevate your career as a Quality Assurance Associate at Catalent's manufacturing facility in Adair, Ontario. Ensure compliance and maintain high-quality standards in pharmaceutical production while working onsite. Join Catalent to help instill a culture of quality compliance and continuous improvement.

As a Quality Assurance Associate, you will perform in-process audits, final product checks, and train staff on cGMP practices. Your contributions will be vital in preventing quality issues in a state-of-the-art facility dedicated to innovation and patient care. Key Responsibilities:
Perform in-process document audits and quality checks
Conduct final release audits of batch documentation
Investigate manufacturing issues and provide coaching
Execute weekly compliance audits in production
Act as QA representative for decision-making Requirements:
Bachelor’s Degree in Science or Engineering required
Comfortable with manual dexterity tasks
Robust analytical and problem-solving skills
Excellent verbal and written communication
Ability to work independently and lead Become part of a team that's transforming lives through quality assurance in pharmaceutical manufacturing at Catalent.

📌 Quality Assurance In Pharmaceutical Manufacturing Strathroy (Canada)
🏢 Catalent Pharma Solutions
📍 Canada