Quality Assurance Associate

Catalent Pharma Solutions • Windsor, ON

8d • CA$48,000 - CA$57,000 • Onsite

About The Position

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 will be on preventing quality issues rather than detecting them. You will also coach and train operators and supervisors on proper documentation practices and current Good Manufacturing Practice (cGMP) requirements.

Requirements

• Bachelor’s degree in science (Chemistry or Biochemistry preferred) is required.
• Experience working in a manufacturing, pharmaceutical, and/or GMP facility is an asset.
• This position does not qualify for sponsorship.
• 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 (ACESC) such as World Education Services (WES).
• 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 cGMPs and Standard Operating Procedures (SOPs), including coaching and training employees and supervisors on each issue.
• Assist in initiating manufacturing events and deviations as 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 production and QA management as required.
• Issue, review, and file various logs from operational areas, including equipment logs and temperature/relative humidity logs.
• Monitor GMP compliance in operating areas to maintain inspection readiness.
• Participate in special projects in other areas of quality and compliance, 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 (RPP) with employer contributions.
• Employee Reward & Recognition programs.
• Opportunities for professional and personal development & growth including tuition reimbursement.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level