Quality Control Laboratory Coordinator (12-month contract)

Quality Control Laboratory Coordinator (12-month contract)

Apply locations Windsor, Canada time type Full time posted on Posted Yesterday time left to apply End Date: March 25, 2025 (25 days left to apply) job requisition id 0088172

Position Summary

Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.

This position is located in Windsor, Ontario, 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.

Reporting to the Quality Control Supervisor, the Quality Control Laboratory Coordinator is accountable for maintaining the GMP compliance, safety, housekeeping, and inventory management of the Quality Control laboratories. The Quality Control Laboratory Coordinator will assist the QC Supervisor with training, resolving testing issues and laboratory investigations as required. The incumbent is responsible to maintain a level of GMP and safety in the laboratories necessary to comply with regulations.

Shifts: Monday - Friday; 8:00 AM-4:30 PM or 8:30 AM-5:00 PM with a 30-minute unpaid lunch

Contract: 12 months

Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee.

The Role:

• Develop and maintain a laboratory inventory management program and prepares purchase orders as needed.
• Directs the housekeeping and daily laboratory maintenance activities.
• Provides assistance to analysts with troubleshooting testing issues.
• Identifies and executes continuous improvement opportunities for the QC laboratories.
• Writes and leads laboratory investigations and deviation investigations as required.
• Provide backup to Quality Control Supervisors.
• Ensure that the laboratory meets a level of GMP to comply with current regulations.
• Perform other duties as assigned.

The Candidate:

• Diploma in Science (Chemistry, Biology, Microbiology) or related field is required, Bachelor’s Degree in Science (Chemistry, Biology, Microbiology) or related field is preferred.
• A minimum of 2+ years of laboratory experience in quality control or related field is preferred.
• Experience working in a manufacturing, pharmaceutical and/or GMP facility is an asset.
• Excellent computer skills in Microsoft Office including Word, Excel, Access and Outlook.
• Excellent time management, organization and interpersonal skills.
• Strong interpersonal skills, essential in dealing with people at all levels and in a variety of functions; able to influence and motivate others to quickly achieve results.
• Demonstrated ability to lead a team and achieve results.
• Ability to prioritize and focus team on appropriate tasks.
• 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 WES.
• 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.

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 life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.