Quality Assurance Supervisor
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.
Position Summary
We have an opportunity for a Quality Assurance Supervisor to join our team. In this role, you will oversee daily priorities for the Quality Assurance team and ensure compliance with cGMP standards throughout the production process. You will be responsible for quality assurance activities, batch release, and maintaining archiving programs. This position plays a key role in supporting quality systems and continuous improvement initiatives.
Shift: Monday -Friday, 8:00 AM-4:30 PM or 8:30 AM-5:00 PM with a 30-minute unpaid lunch
Location: Strathroy, ON
100% Onsite
The Role
Communicate daily work plans and priorities with the Quality team to meet product release timelines and expectations.
Collaborate with functional areas to resolve quality issues and ensure product compliance with cGMP, SOPs, and standards.
Lead, coordinate, and participate in investigations and corrective actions for deviations and documentation issues, ensuring timely closure.
Work closely with operations to support the quality management system and provide guidance on cGMP and SOP compliance during production and packaging.
Ensure all manufacturing batch documents for finished products are properly maintained and controlled.
Review and approve quality documents, including Master Batch Production Records, specifications, directives, reports, and SOPs.
Liaise with customer QA contacts regarding quality issues and agreements.
Provide leadership, motivation, and training for employees, monitoring performance in line with company policies.
Perform other duties as required.
The Candidate
Minimum Requirements
Bachelor’s degree in science, engineering (chemistry, biochemistry), or a related field required.
3+ years of experience in QA/QC or a related field required., with at least 1 year of supervisory experience preferred.
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.
Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent‑sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.
Preferred Skills & Background
Experience working in manufacturing, pharmaceutical, and/or GMP facilities preferred.
Understanding of overall business needs and objectives.
Expertise in tools to meet current and advancing cGMP requirements.
Excellent verbal and written communication skills.
Ability to multi-task and prioritize effectively.
Ability to respond quickly to a changing regulatory environment.
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.
Currently, Catalent participates in the Ontario Immigrant Nominee Program (OINP) on a limited basis.
Pay
The final salary offered to a successful candidate may vary within this range $65,000 – $81,000, 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 including health, dental, vision, and life insurance.
Group retirement savings with employer contributions.
Employee reward and recognition programs.
Opportunities for professional and personal development, 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 [email protected]. 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.
Skills Required
- Bachelor's degree in science or engineering (chemistry, biochemistry) or related field
- 3+ years of experience in QA/QC or a related field
- At least 1 year of supervisory experience
- Ability to communicate (talk and hear); perform manual dexterity tasks; occasional standing, walking, bending; potential exposure to chemicals (physical demands)
- Demonstrable leadership experience at Catalent may be considered in place of external experience
- Experience working in manufacturing, pharmaceutical, and/or GMP facilities
- Candidates with non-Canadian credentials must provide an evaluation confirming Canadian equivalency (e.g., WES/ACESC)
- Excellent verbal and written communication, ability to multi-task, prioritize, and respond to changing regulatory environment
Catalent, Inc. Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Catalent, Inc. and has not been reviewed or approved by Catalent, Inc..
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Leave & Time Off Breadth — Paid time off is commonly described as roughly 152 hours per year plus about eight paid holidays for U.S. roles. Eligibility and exact counts vary by location, but the allotment is positioned as competitive.
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Retirement Support — A 401(k) with a company match (often described as dollar‑for‑dollar up to 6%) is part of the package. The match level is commonly referenced as a meaningful component of total rewards.
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Inclusive Benefits Coverage — Medical, dental, vision, life/disability, HSA/FSA, EAP, tuition reimbursement, adoption assistance, commuter and dependent‑care benefits, and wellness programs are offered. Some roles indicate benefits eligibility begins on the first day for direct hires.
Catalent, Inc. Insights
What We Do
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. For more information, visit www.catalent.com.
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