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
- Solid 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 (Toronto)
🏢 Catalent Pharma Solutions
📍 Toronto