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Catalent Pharma Solutions

Quality Management System Specialist

Strathroy, ON, Canada
CAN-Strathroy ON Adair, Canada

Pay: The final salary offered to a successful candidate may vary within this range $56,000 – $65,000, 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
Experience: Minimum of 2 years of experience in Quality, Operations, or related field required.
Posting language: English
Posted: Sep 29, 2026

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Original job description

About Site

The newly launched manufacturing facility on Adair Blvd marks a pivotal expansion of Catalent’s Zydis® technology, a globally renowned, fast-dissolve oral dosage form that has transformed the lives of millions of patients worldwide. This is your opportunity to join a dedicated team at the forefront of pharmaceutical manufacturing. At Adair, you’ll play a vital role in the startup of a site built for innovation and excellence, from installation and qualification to regulatory approval and commercial manufacturing.

Position Summary

We have an opportunity for a Quality Management System Specialist to join our team. In this role, you will maintain the company’s quality management systems to ensure compliance with Good Manufacturing Practices. You will organize and conduct assessments related to suppliers, product complaints, internal compliance, and change control. This position plays a key role in fostering a culture of continuous improvement and operational excellence at the Adair site.

Shift: Monday - Friday, 8:00 AM – 4:30 PM or 8:30 AM – 5:00 PM with a 30-minute Location: Adair, ON 100% Onsite

The Role

Participate in various quality system areas, including customer regulatory inquiries, change control, document control, and metrics provision.
Maintain the facility’s supplier assessment program, reviewing supplier audit reports, complaints, and material reviews.
Lead the internal audit schedule, support self-inspections, review audit reports, and assist with regulatory and customer audits to ensure compliance and inspection readiness.
Support the preparation of Quality Systems trend reports, provide recommendations based on observed trends, and lead or support continuous improvement initiatives.
Participate in investigations and corrective action identification or implementation for deviations and complaint documentation, ensuring timely closure.
Conduct compliance reviews of site and corporate procedures and support quality improvement initiatives by participating in project teams and executing assigned projects.
Develop the Quality Management System for optimal efficiency by leading small teams through the implementation of new systems and ways of working.
Perform other duties as required.

The Candidate

Minimum Requirements

Diploma or bachelor’s degree in life science or related field required.
Minimum of 2 years of experience in Quality, Operations, or related field required.
Experience working in a regulated manufacturing environment required.
Previous experience in Quality Management System, preferably within the pharmaceutical industry, is highly desirable.
Experience in preparation and involvement relating to FDA and HPFBI inspections is desirable.
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, twist, stoop, kneel, crouch, or crawl. Vision abilities required include close vision.

Preferred Skills & Background

Knowledge of Good Manufacturing Practice compliance and regulatory requirements with a strong understanding of quality systems.
Experience in generating controlled documents.
Strong attention to detail and a high degree of accuracy.
Excellent organizational and time management skills to prioritize tasks, allocate resources effectively, and meet schedules.
Demonstrated ethics and due diligence.
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.
Excellent communication (written and verbal) and interpersonal skills.
Strong computer skills including Microsoft Office Suite (Outlook, Excel, PowerPoint, Word) and familiarity with quality management systems and related software is advantageous.
Ability to respond quickly to a changing regulatory environment.

Pay

The final salary offered to a successful candidate may vary within this range $56,000 – $65,000, 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 (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.

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More about this job

Responsibilities

The Quality Management System Specialist maintains quality systems to ensure compliance with Good Manufacturing Practices and regulatory standards. They lead internal audits, manage supplier assessments, and drive continuous improvement initiatives across the facility.

Requirements

Candidates must hold a diploma or bachelor's degree in a life science field and possess at least 2 years of experience in quality or manufacturing. Strong knowledge of regulatory requirements and proficiency in quality management software are essential for this role.

Skills

Quality management systems
Good manufacturing practices
Supplier assessment
Internal auditing
Change control
Document control
Regulatory compliance
Continuous improvement
Deviation investigation
Corrective action
Microsoft office suite
Time management
Attention to detail
Communication skills
Interpersonal skills

Benefits

Health insurance
Dental insurance
Vision insurance
Life insurance
Group retirement savings
Registered pension plan
Tuition reimbursement

Visa sponsorship

Not detected in the job text

Keywords

Quality Management System
Good Manufacturing Practice
Pharmaceutical
Compliance
Regulatory Affairs
Audit
Supplier Assessment
Change Control
Document Control
Continuous Improvement
Deviation
Corrective Action
Life Science
Microsoft Office
FDA
HPFBI
Manufacturing
Zydis technology
Operational Excellence

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