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. #J-18808-Ljbffr