Join Catalent as a Quality Assurance Associate in Adair, ON and play a key role in pharmaceutical product compliance. Contribute to manufacturing excellence through audits and staff training. This position emphasizes maintaining high quality and compliance standards in pharmaceutical production. You will perform critical audits and assist in coaching employees on best practices while supporting the facility's creative startup phase. Key Responsibilities:
Conduct in-process audits and relay findings to production
Ensure compliance through final release document audits
Investigate deviations and coach staff on improvement
Execute compliance audits and generate management reports
Act as QA representative to resolve manufacturing issues
Requirements:
Bachelor’s Degree in a relevant scientific field
Excellent manual dexterity and attention to detail
Solid analytical and communication skills
Able to work self-sufficiently with little oversight
Experience in a pharmaceutical or GMP setting is a plus
Help elevate product quality and contribute to patient outcomes at Catalent's state-of-the-art facility.