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Added 6 mins ago
MN
Safety Consultant
Matchtech North America
Toronto, ON · Greater Toronto Area, Canada
- Full-time
Lead safety assessment processes, including hazard identification, risk analysis, and safety requirements allocation.
Added 6 mins ago
HT
Engineering Team Leader (PET HR)
Husky Technologies
Bolton, ON
- Full-time
Plan, organize and lead a design team for new product development with adherence to Product Development Process, Husky Standards and Stage Gate. Responsibilities include estimating effort…
Added 6 mins ago
HT
Internal Auditor (Business Control & IT)
Husky Technologies
Bolton, ON
- Full-time
…passion of our people around the world and their desire to lead change. At the same time, we are not afraid to expect a lot and strive for leadership in all of our key markets. We are a…
Added 6 mins ago
HT
Manager, Internal Controls
Husky Technologies
Bolton, ON
- Full-time
Recommend improvements in the design of business processes and internal controls and lead the implementation of initiatives
Added 6 mins ago
HT
CNC Programmer
Husky Technologies
Bolton, ON
- Full-time
Lead and perform troubleshooting to generate multiple hypotheses regarding the causes of a problem by employing methodical, logical approaches to problem solving
Added 6 mins ago
MN
Electrical Engineer
Matchtech North America
Toronto, ON · Greater Toronto Area, Canada
- Full-time
Interface with clients, stakeholders, and authorities by providing technical input, progress updates, and support during design and implementation phases.
Added 6 mins ago
NB
Senior Advisor Consumer Protection Compliance
National Bank of Canada
Montreal, QC
- Full-time
Lead the design, implementation, and continuous enhancement of the
Added 7 mins ago
UO
Labour Relations Consultant
University of Waterloo
Waterloo, ON
- Full-time
Contributes to the development, implementation, and continuous improvement of labour relations policies, programs, practices, and resources.
Added 7 mins ago
UO
Undergraduate Student Relations Officer
University of Waterloo
Waterloo, ON · Mathematics & Computer
- Full-time
The Undergraduate Student Relations Officer will provide direction on the implementation of initiatives that develop, support and guide strategies that increase student engagement and…
Added 7 mins ago
SH
Registered Nurse (RN) - CICU - Sponsorship - FT
Southlake Health Community
Newmarket, ON · Southlake Health
- Full-time
Combination of instructor lead virtual and clinical education
Added 7 mins ago
SH
Nurse Educator, Temporary Full Time - Magna Outpatient Cancer Centre
Southlake Health Community
Newmarket, ON · Southlake Health
- Full-time
Leads the development, implementation, and evaluation of clinical pathways and patient care guidelines as it relates to the episodes of care within the clinical area.
Added 7 mins ago
SH
Registered Nurse - Emergency Department
Southlake Health Community
Newmarket, ON · Southlake Health
- Full-time
Assists in the development and implementation of the Plan of Care and evaluates its ongoing effectiveness.
Added 7 mins ago
SH
Registered Nurse - Clinical Resource Team (CRT)
Southlake Health Community
Newmarket, ON · Southlake Health
- Full-time
Assists in the development and implementation of the Plan of Care and evaluates its ongoing effectiveness.
Added 7 mins ago
SH
Registered Nurse, Vascular Access Team - Temporary Part Time
Southlake Health Community
Newmarket, ON · Southlake Health
- Part-time
The Vascular Access Nurse will work collaboratively to ensure the development and implementation of best practices for vascular access and vascular access devices. Consistent application of…
Added 7 mins ago
SH
Registered Nurse - Clinical Resource Team (CRT)
Southlake Health Community
Newmarket, ON · Southlake Health
- Full-time
Assists in the development and implementation of the Plan of Care and evaluates its ongoing effectiveness.
Added 7 mins ago
Registered Nurse, Vascular Access Team - Temporary Casual
Southlake Health Community
Newmarket, ON · Southlake Health
The Vascular Access Nurse will work collaboratively to ensure the development and implementation of best practices for vascular access and vascular access devices. Consistent application of…
Added 7 mins ago
SH
Disability Case Specialist - Full Time
Southlake Health Community
Newmarket, ON · Southlake Health
- Full-time
Contribute to the development, implementation, and ongoing refinement of policies, procedures, and standardized tools related to disability management, chronic condition support,…
Added 23 mins ago
MS
Consultant Conversion - Lead Cybersecurity Eng : Job Level - Director
Morgan Stanley
Montreal, QC
- Full-time
…markets and shape the future of our communities. This is a Lead Cybersecurity Engineering position at Director level, which is part of the job family responsible for cybersecurity…
Added 23 mins ago
M
Senior Full Stack Java Engineer
Miratech
Canada
- Full-time
…fundamentals who can take features from technical design through implementation, testing, deployment, and production support. Experience with Workforce Management (WFM), Customer Experience…
Added 37 mins ago
SP
RVP, Sales - Data Foundation - Public Sector
Salesforce Partner Canada
ON · Ontario, Canada
- Full-time
…for personalized engagement, and Professional Services for implementation support - to ensure customers have the trusted, unified data infrastructure needed to power AI and automation at…
Added 52 mins ago
E
Test Manager ISAC System Verification
Ericsson
Ottawa, ON
- Full-time
Lead test management activities across multiple quality areas and verification domains.
Added 1 hour ago
M
Senior Full Stack Java Engineer
Miratech
Canada
- Full-time
…fundamentals who can take features from technical design through implementation, testing, deployment, and production support. Experience with Workforce Management (WFM), Customer Experience…
Added 1 hour ago
TC
Project Manager
ThirdEye CyberSecurity
Regina, SK
- Contract
…technology experience. This Project Manager will manage the implementation of clinically focused information technology projects. This may include managing multiple complex projects…
Added 1 hour ago
VT
FileNet IER Developer
Viva Tech Solutions
Toronto, ON
- Contract
We are seeking an experienced Subject Matter Expert (SME) for the IER module to lead the design, development, and implementation of customized integrations aligned with business…
Added 1 hour ago
H(
Technical Lead, API & Integration Engineering
HOOPP (Healthcare of Ontario Pension Plan)
Toronto, ON · CA ON Toronto
- $103,000 to $153,000 CAD / year
- Full-time
You will act as a hands-on technical lead for product development initiatives, balancing delivery leadership with engineering depth. This role will provide technical mentorship to…

Catalent

Quality Management System Specialist

Strathroy-Caradoc, ON, Canada
Strathroy, ON, N7G 3H8, Canada

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. · Full-time

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Job details

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
Education: Bachelor’s degree
Experience: Minimum of 2 years of experience in Quality, Operations, or related field required.
Posting language: English
Posted: Oct 4, 2026

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

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. Familiarity with regulated environments and strong documentation skills are essential for this role.

Skills

Quality management systems
Good manufacturing practices
Supplier assessment
Internal auditing
Regulatory compliance
Change control
Document control
Continuous improvement
Deviation investigation
Corrective action implementation
Trend reporting
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
Employer contributions
Employee reward and recognition programs
Professional and personal development opportunities
Tuition reimbursement

Visa sponsorship

Not detected in the job text

Keywords

Quality Management System
Good Manufacturing Practice
Pharmaceutical manufacturing
Regulatory approval
Compliance
Supplier audit
Product complaints
Change control
Document control
Internal audit
Self-inspections
FDA
HPFBI
Corrective action
Deviations
Microsoft Office
Outlook
Excel
PowerPoint
Word
Life science
Operational excellence
Quality improvement
Inspection readiness
Trend analysis

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