Quality Control - Analytical Laboratory Supervisor (12-month contract)
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 Manager, the Quality Control Analytical Laboratory Supervisor is accountable for the direct supervision of the relevant Quality Control laboratory personnel, activities and programs. The Quality Control Analytical Laboratory Supervisor 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
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:
Accountable for ensuring that samples are tested accordingly and results reported on time.
Perform timely and effective investigations of out-of-specification and out-of-trend test data.
Ensure that the laboratory meets a level of GMP to comply with current regulations.
Ensure that excellent documentation. controls and capabilities are in place to maintain data integrity and ensure timely and effective actions are taken.
Schedule testing according to performance expectations.
Provide training to laboratory personnel in analytical procedures, instrumentation and regulatory requirements.
Supervise laboratory equipment maintenance and calibration programs.
Perform other duties as required.
The Candidate:
Bachelor’s degree in science, Chemistry or related field is required.
Minimum 5+ years of experience in analytical chemistry preferred.
Experience working in a pharmaceutical and/or GMP facility is an asset.
Knowledge of laboratory techniques, terminology, equipment and materials.
Knowledge of the principles and practices of chemical, biological and physical testing and analyses including the preparation of materials, equipment and samples.
Ability to perform multiple tasks concurrently with accuracy.
Demonstrate applicable ethics and due diligence.
Strong interpersonal skills in dealing with people at all levels and in a variety of functions; able to influence and motivate others to quickly achieve results.
While performing the responsibilities of the job, the employee is required to talk and hear.
The employee is often required to sit and use their hands and fingers, to handle or feel and to manipulate keys on a keyboard. Use of manual dexterity is required.
The employee is occasionally required to stand, walk, reach with arms and hands, bend or twist, and to stoop, kneel, crouch or crawl.
Vision abilities required by this job include close vision.
There is also the 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.
Visit Catalent Careers to explore career opportunities.
Catalent is an Equal Opportunity Employer and does not discriminate based on any characteristic protected by local law.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.