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