Quality Assurance in Pharmaceutical Manufacturing

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

• Strong 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.