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Added 9 mins ago
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Catalent Pharma Solutions

Quality Assurance Supervisor

Strathroy, ON, Canada
CAN-Strathroy Ontario, Canada

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. · Full-time

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Job details

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.
Job type: Full-time
Apply by: Oct 26, 2026
Education: Bachelor’s degree
Posting language: English
Posted: Sep 28, 2026

Original job description

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

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 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.

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More about this job

Responsibilities

The Quality Assurance Supervisor is responsible for overseeing quality control processes and ensuring adherence to company standards. They will lead the quality team to maintain product integrity and drive continuous improvement initiatives.

Requirements

Candidates should have previous experience in a quality assurance or supervisory role within a manufacturing environment. Strong leadership skills and a thorough understanding of quality management systems are required.

Skills

Quality Assurance
Supervision
Quality Control
Process Improvement
Compliance
Team Leadership
Reporting

Visa sponsorship

Not detected in the job text

Keywords

Quality Assurance
Supervisor
Manufacturing
Quality Control
Compliance
Process Improvement
Quality Management Systems

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