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Added 11 mins ago
Assistant / Associate / Full Professor - Academic General Internist
University of Toronto
Toronto, ON
…(CQI) or a Clinician Teacher (CT), at the rank of Assistant, Associate or Full Professor. It is expected that the position will be approximately 70% clinical and 30% related to quality…
Added 1 hour ago
OS
(TEMPORARY FULL TIME) SENIOR CLINICAL RESEARCH ASSOCIATE - RESEARCH AND ACADEMICS
Ontario Shores Centre for Mental Health Sciences
Whitby, ON
- Full-time
The Applied Mental Health Research Group at Ontario Shores Centre for Mental Health Sciences is currently seeking a Senior Research Associate (SRA) to assist in managing exciting…
Added 1 hour ago
AH
Clinical Research Coordinator - Phase 1 Group
Alberta Health Services
AB · Greater Edmonton Metropolitan Area
- Temporary
Are you an experienced clinical trial professional looking to work with cutting-edge cancer therapies? We are seeking a dynamic Clinical Trials Coordinator to join our Clinical Trial Unit…
Added 3 hours ago
CS
Assistant, Associate, or Full Professor, Plastic and Reconstructive Surgery - Sunnybrook Health Sciences Centre
Canadian Society of Plastic Surgeons
Toronto, ON · Greater Toronto Area, Canada
- Full-time
Sunnybrook Health Sciences Centre is one of Canada’s largest hospitals and a leader in clinical and research activities. Sunnybrook Health Sciences Centre is a fully affiliated academic…
Added 3 hours ago
PH
Associate Legal Counsel, PHSA Legal Services
Provincial Health Services Authority
Vancouver, BC
- Full-time
Respond to a variety of legal issues that affect the healthcare industry and the clinical and business operations of PHSA.
Added 5 hours ago
LC
Associate Faculty - Clinical Nursing
Lambton College
Sarnia, ON
- Part-time
We are providing our students with the best learning and research experiences to ensure they are well-equipped to contribute to, and thrive in, a world of opportunity.
Added 10 hours ago
MU
Laboratory Technician
McGill University
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- Full-time
Demonstrated ability to work with clinical and administrative information systems such as Medesync is a very strong asset.
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Quality Assurance Associate
Catalent
Strathroy-Caradoc, ON · Strathroy, Ontario
- Full-time
We have an opportunity for a Quality Assurance Associate to join our team and help create a culture of quality compliance and continuous improvement. This role focuses on preventing quality…
Added 15 hours ago
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Veterinary Technologist, Emergency, Guardian Veterinary Centre
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Added 17 hours ago
LC
Associate Faculty - Clinical Nursing
Lambton College
Sarnia, ON
- Part-time
We are providing our students with the best learning and research experiences to ensure they are well-equipped to contribute to, and thrive in, a world of opportunity.
Added 1 day ago
UO
Veterinary Technician, Animal Care
University of Ottawa
Ottawa, ON · University of Ottawa Heart Institute
- Full-time
Reporting to the Associate-Supervisor, Animal Care Operations, the incumbent participates in the delivery of the program of veterinary care under the general supervision of a veterinarian…
Added 1 day ago
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Clinical Research Manager
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
…following established governmental guidelines and regulations, the Clinical Trial Project Manager is responsible for the operational management of multicentre clinical research studies. The…
Added 1 day ago
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Project Manager, Capture and Optimization of Research Data (CORD) Platform
RI-MUHC | Research Institute of the MUHC | #rimuhc
Montreal, QC
- Full-time
The Research Institute of the MUHC is seeking an interim Project Manager to join the Capture and Optimization of Research Data (CORD) platform of the Centre for Outcomes Research and…
Added 2 days ago
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Strong knowledge of patient care, anesthesia, pharmacology, and clinical procedures.
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Dental Assistant
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Montreal, QC
- Full-time
…of instruments, materials and supplies used in clinics and research and teaching laboratories. Develops…
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Veterinary Technologist, Frontier Animal Hospital
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Saskatoon, SK
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Experience in a veterinary hospital or clinical setting is an asset.
Added 3 days ago
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Quality Assurance Associate
Catalent Pharma Solutions
Strathroy, ON · CAN-Strathroy ON Adair
- Full-time
We have an opportunity for a Quality Assurance Associate to join our team and help create a culture of quality compliance and continuous improvement. This role focuses on preventing quality…
Added 3 days ago
CP
Quality Assurance Associate
Catalent Pharma Solutions
Strathroy, ON · CAN-Strathroy Ontario
- Full-time
We have an opportunity for a Quality Assurance Associate to join our team. In this role, you will help create a culture of quality compliance and continuous improvement that meets…
Added 3 days ago
AH
Associate Physician - Diagnostic Imaging
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Pediatric Neurology in the Department of Pediatrics, Alberta Health Services, invites applications for a full‑time Associate Physician position. The successful candidate will provide…
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Emergency Registered Veterinary Technician - Etobicoke, ON
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Toronto, ON
High school diploma or equivalent and associate’s degree or higher in veterinary technology from an accredited program required
Added 3 days ago
SJ
IIWCC - Registered Practical Nurse
St. Joseph's Home Care
Hamilton, ON
- $27.52 to $29.84 CAD / hour
- Full-time
Apply current knowledge and research of Wound Care Protocol to practice.
Added 3 days ago
SJ
NSWOC - Registered Nurse
St. Joseph's Home Care
Hamilton, ON
- $31.39 to $46.47 CAD / hour
- Full-time
Apply current knowledge and research of Wound Care Protocol to practice.
Added 3 days ago
SJ
IIWCC - Registered Nurse
St. Joseph's Home Care
Hamilton, ON
- $31.39 to $46.47 CAD / hour
- Full-time
Apply current knowledge and research of Wound Care Protocol to practice.

Catalent Pharma Solutions

Quality Assurance Associate

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

The final salary offered to a successful candidate may vary within this range $48,000 – $55,000, 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 $48,000 – $55,000, 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 Associate

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 Assurance Associate to join our team and help create a culture of quality compliance and continuous improvement. This role focuses on preventing quality issues and ensuring compliance with government, customer, and business requirements. You will be involved in final product audits, coaching and training on documentation practices, and supporting cGMP standards. Your work will contribute to maintaining the highest quality standards in pharmaceutical manufacturing.

Shift: 8-12 hour rotating continental shifts as defined by rotation schedule. Location: Adair, ON 100% Onsite

The Role

Perform in-process document auditing and product quality checks in production, ensuring all issues are communicated to production employees, management, and QA management, including QA sign-off after set-up to confirm compliance with batch documentation and SOPs.
Conduct final release auditing of batch documentation to ensure products are manufactured in compliance with cGMP and SOPs, including all duties required for final product release.
Assist in investigating manufacturing issues and deviations reported by production departments; coach and train operators and supervisors on cGMP practices.
Perform weekly compliance audits in production and packaging departments and prepare reports for QA management.
Act as QA representative on shift for decision-making and issue resolution, escalating serious issues as required.
Assist in writing and revising SOPs and support filing, archiving, and review of quality documents.
Perform finished product blister inspection prior to batch release.
Perform other duties as assigned.

The Candidate

Minimum Requirements

Bachelor’s Degree in Science, Engineering (Chemistry, Biochemistry) or related field required.
This position does not qualify for sponsorship.
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.
The role frequently involves sitting and utilizing hands and fingers for tasks such as handling, feeling, and keyboard manipulation, requiring manual dexterity.
Occasionally requires standing, walking, reaching, bending, twisting, stooping, kneeling, crouching, or crawling, alongside close vision capabilities and potential exposure to chemicals.

Preferred Skills & Background

No previous experience required.
Prior experience in a manufacturing, pharmaceutical, and/or GMP facility would be an asset.
Strong analytical and problem-solving skills.
Extremely detail-oriented.
Excellent communication skills – verbal and written.
Able to work independently with minimal supervision.
Experience with coaching or leadership, with the ability to give feedback and implement a quality culture on the production floor.

Pay

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 Assurance Associate will perform in-process document auditing, product quality checks, and final release auditing to ensure compliance with cGMP and SOPs. They will also assist in investigating manufacturing deviations and provide coaching to production staff on quality practices.

Requirements

Candidates must hold a Bachelor’s degree in Science or Engineering (Chemistry, Biochemistry). The role requires strong analytical skills, attention to detail, and the ability to work in a 100% onsite manufacturing environment.

Skills

Quality assurance
cGMP
SOP compliance
Document auditing
Batch documentation
Analytical skills
Problem-solving
Coaching
Leadership
Detail-oriented
Communication
Pharmaceutical manufacturing
Regulatory compliance
Technical writing

Benefits

Health insurance
Dental insurance
Vision insurance
Life insurance
Group retirement savings
Registered pension plan
Employee reward and recognition programs
Tuition reimbursement

Visa sponsorship

Not detected in the job text

Keywords

Quality Assurance
Pharmaceutical Manufacturing
cGMP
SOP
Batch Documentation
Compliance
Auditing
Chemistry
Biochemistry
Engineering
Zydis technology
Packaging
Production
Regulatory Approval
Quality Compliance
Continuous Improvement
Blister Inspection
Manufacturing Deviations

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