Quality Assurance Associate (Contract position - 11 months)
About The Position
Catalent’s Windsor, Ontario facility is a modern site dedicated to the development and manufacturing of softgel technologies for the pharmaceutical and consumer health industries. The location supports a wide range of products and services, providing an environment where innovation and quality are at the forefront. With advanced capabilities and a strong focus on collaboration, the Windsor site plays a key role in delivering solutions that improve patient health worldwide. This dynamic setting offers employees the opportunity to work with cutting-edge technologies and contribute to meaningful projects in a supportive and professional atmosphere. We have an opportunity for a Quality Assurance Associate (Contract position - 11 months) to join our team. In this role, you will help create a culture of quality, compliance, and continuous improvement. You will focus on preventing quality issues and support operators and supervisors with training on proper documentation and current Good Manufacturing Practice requirements. This position plays a key role in ensuring compliance and maintaining high standards across operations.
Requirements
- Bachelor’s degree in science (Chemistry or Biochemistry preferred) is required.
- Experience working in a manufacturing, pharmaceutical, and/or Good Manufacturing Practice facility is an asset.
- Candidates with non-Canadian credentials must provide an evaluation confirming the Canadian equivalency of the credentials as determined by the Alliance of Credential Evaluation Services of Canada such as World Education Services.
- The role frequently involves sitting and using hands and fingers for tasks such as handling, feeling, and keyboard manipulation, requiring manual dexterity.
- Occasionally, it requires standing, walking, reaching, bending, twisting, stooping, kneeling, crouching, or crawling, along with close vision capabilities and potential exposure to chemicals.
Nice To Haves
- Advanced computer skills in Microsoft Office Suite (Outlook, Excel, Access, Word).
- Strong analytical and interpersonal skills.
- Extremely detail-oriented.
- Excellent verbal and written communication skills.
- Able to work independently with minimal supervision.
Responsibilities
- Perform in-process batch review of documentation to ensure compliance with current Good Manufacturing Practices and Standard Operating Procedures, including coaching and training employees and supervisors on identified issues.
- Assist in initiating manufacturing events and deviations reported by production departments, ensuring product with potential quality issues is acceptable for release and reports are updated.
- Perform line clearance verifications of equipment and processing areas during product changeovers, which may include testing and verification of vision equipment.
- Act as Quality Assurance representative on shift for decision-making and issue resolution, escalating serious issues to management as required.
- Issue, review, and file various operational logs, including equipment and temperature/relative humidity logs.
- Monitor Good Manufacturing Practice compliance in operating areas to maintain inspection readiness.
- Participate in special projects in other quality and compliance areas and work extended hours or weekends as needed to meet deadlines or resolve issues.
- Perform other duties as required.
Benefits
- Comprehensive Benefit Package (Health, Dental, Vision, & Life Insurance).
- Group Retirement Savings – Registered Pension Plan with employer contributions.
- Employee Reward & Recognition programs.
- Opportunities for professional and personal development and growth, including tuition reimbursement.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
