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 productionEnsure compliance through final release document auditsInvestigate deviations and coach staff on improvementExecute compliance audits and generate management reportsAct as QA representative to resolve manufacturing issuesRequirements:Bachelor's Degree in a relevant scientific fieldExcellent manual dexterity and attention to detailStrong analytical and communication skillsAble to work self-sufficiently with little oversightExperience in a pharmaceutical or GMP environment is a plusHelp elevate product quality and contribute to patient outcomes at Catalent's state-of-the-art facility.