Quality Assurance Associate

About Site Strathroy, Ontario is one of two sites located in Canada offering softgel development and manufacturing capabilities for the Pharmaceutical and Consumer Health industries. We have a broad range of integrated formulation, manufacturing, analytical and packaging services to offer full-service turnkey solutions.

Summary We have an opportunity for a Quality Assurance Associate to join our team. In this role, you will help create a culture of quality compliance and continuous improvement that meets government, customer, and business requirements. The focus is on preventing quality issues rather than detecting them. You will support product release, coach and train operators on documentation practices, and ensure compliance with current Good Manufacturing Practices (cGMP). Shift: 12-hour Continental Shifts (Days and Nights- 7:00 AM – 7:00 PM or 7:00 PM – 7:00 AM) Location: Strathroy, ON 100% Onsite The Role Perform in-process document auditing and product quality checks in production and communicate issues to production employees, management, and QA management. Conduct Final Release auditing of batch documentation to ensure compliance with cGMP and Standard Operating Procedures, including all duties required for final product release. Assist in investigating manufacturing issues and deviations reported by production departments. Perform in-process product quality checks and documentation review. Carry out weekly compliance audits in production and packaging departments and prepare reports for QA management. Act as QA representative on shift for decision-making and issue resolution, escalating serious issues as needed. Perform line clearance verifications during product changeovers, including testing or verification of vision equipment. Perform other duties as assigned. The Candidate Minimum Requirements Bachelor’s Degree in Science, Engineering (Chemistry, Biochemistry) or related field required. Prior experience in a manufacturing, pharmaceutical, and/or Good Manufacturing Practice facility would be an asset. The employee's role frequently involves sitting and utilizing hands and fingers for tasks such as handling, feeling, and keyboard manipulation, necessitating manual dexterity. Occasionally, the position requires standing, walking, reaching, bending, twisting, stooping, kneeling, crouching, or crawling, alongside close vision capabilities and potential exposure to chemicals. Preferred Skills & Background No previous experience required. Strong analytical and problem-solving skills. Extremely detail-oriented. Excellent prioritization and time management skills. Strong interpersonal skills. Excellent verbal and written communication skills. Able to work independently with minimal supervision. Advanced computer skills in Microsoft Excel and Word. Candidates with non-Canadian credentials must provide an evaluation confirming Canadian equivalency as determined by the Alliance of Credential Evaluation Services of Canada (ACESC) such as WES. This position does not qualify for sponsorship. Pay The final salary offered to a successful candidate may vary within this range $48,000 – $59,000, and will be dependent on several factors that may include but are not limited to: the type and length of experience within the job, type and length of experience within the industry, skillset, education, business needs, etc. Catalent is a global employer, and this salary range does not reflect positions that work in other countries. Why You Should Join Catalent Comprehensive Benefit Package (Health, Dental, Vision, & Life Insurance). Group Retirement Savings – Registered Pension Plan (RPP) with employer contributions. Employee Reward & Recognition programs. Opportunities for professional and personal development & growth including tuition reimbursement. Catalent offers rewarding opportunities to further your career!   Join the global drug development and delivery leader and help us bring over 7,000 life-saving and