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Added 25 mins ago
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Added 25 mins ago
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$90,000 to $100,000 CAD / year
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Closed listing

CanPrev

Quality Assurance Supervisor 12-month contract

Toronto, ON, Canada
North York, ON, Canada

Pay: Pay: CA$63,000.00-CA$75,000.00 per year
Job type: Full-time
Closing date: Oct 25, 2026
Experience: Minimum 5 years of experience in quality leadership roles within NHP, pharmaceutical or food manufacturing environments.
Posting language: English
Posted: Sep 25, 2026

This opening has closed.

The original listing is kept below for reference.

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Original job description

Archived listing. The details below describe a past opening.

Job description:

About Us:

CanPrev Natural Health is a dynamic and innovative company dedicated to creating exceptional products in the natural health industry. Born from a passion to make natural medicine safe, effective, and accessible to everyone, we’ve been empowering Canadians to take charge of their health for over two decades.

Our team is driven by innovation, collaboration, and a shared commitment to helping people live healthier, more vibrant lives.

Position Overview:

The Quality Assurance Supervisor (contract) will cover maternity leave for 12 months. The position will play a key role in leading the quality team and ensuring compliance with Natural Health Product Regulations (NHPR) following NHP GMP guidelines at CanPrev site. This role is responsible for supervising team activities, managing documentation, driving compliance initiatives, and implementing GMP in collaboration with internal teams and other stakeholders.. The ideal candidate is a results-driven self-starter with strong experience in quality management systems and a proven ability to ensure operational excellence and regulatory adherence.

Key Responsibilities:

Supervise and provide daily guidance to the quality team to ensure activities are performed effectively and in compliance with established standards.
Establish quality key performance criteria and specifications; assess and identify resource requirements to support quality objectives.
Develop, review and update SOPs, forms, and work instructions to maintain regulatory compliance and operational efficiency.
Develop, update, and manage Finished Product Specifications (FPS) in collaboration with the Product Development team and contract manufacturer.
Conduct root cause investigation for quality issues, including Out of Specification (OOS) cases, assign, implement and monitor corrective and preventive action (CAPA).
Manage planned and unplanned deviation in collaboration with contract manufacturers and internal operations teams; conduct risk assessments and provide recommendations.
Develop, maintain, and renew Quality Agreements with contract manufacturers, suppliers, distributors and warehouse service providers.
Approve finished product specifications (FPS), testing parameters, and methodologies in accordance with Health Canada’s Quality of Natural Health Products Guide, USP and other recognized pharmacopoeias.
Oversee change control activities to ensure documents are reviewed and approved on time.
Review and approve change requests, conduct risk assessments, and provide recommendations for the change with appropriate record-keeping.
Lead quality compliance activities in alignment with Natural Health Products Regulatory Regulations (NHPR) following the NHP GMP guidance document to ensure ongoing GMP compliance at Canprev site.
Perform statistical process control including process monitoring, trend analysis, and identification of continuous improvement opportunities.
Conduct internal audits (annual/quarterly), prepare audit reports, follow up on non-conformance, and support external audits and regulatory inspections.
Perform risk analysis of products and processes to create risk assessment matrices to identify, evaluate, and mitigate potential quality and compliance risks.
Identify training needs and manage the employee training matrix.
Design and implement process validation for new products and significant modification to an existing product manufacturing process.
Supervise and approve finished product stability study to ensure compliance with shelf-life claims.
Lead the review of customer feedback, conduct investigation and risk assessment, implement CAPA, and manage response to customers.
Establish qualification criteria for new suppliers and contract manufacturers, evaluate their compliance, and conduct performance re-evaluation of existing contract manufacturers or suppliers.
Monitor and manage eQMS activities to ensure ongoing compliance.
Oversee Preventive Control Plan (PCP) for dietary supplements products.
Perform other related duties as assigned.

Key Qualifications

Bachelor’s degree in Quality Assurance, Life Science, Food Science, or a related scientific/technical field, with a strong foundation in Natural Health Product (NHP) safety and Quality Management Systems.
Minimum 5 years of experience in quality leadership roles within NHP, pharmaceutical or food manufacturing environments.
Solid understanding of GMP requirements, including SOR/2003-196 (Natural Health Product Regulations -NHPR) and 21 CFR Part 111 (cGMP for Dietary Supplements)
Proven experience developing and maintaining SOPs, forms, and process flowcharts.

Key Skills

Experience working with eQMS and manufacturing software systems
Proficiency in Google Workspace (Docs, Sheets, Drive, etc.)
Collaborative and team-oriented mindset
Ability to work independently and manage priorities effectively
Quality-related certification or degree considered an asset
Experience working in NHP GMP-regulated environments
Demonstrated experience leading small to mid-sized quality teams

Nice to Haves

Knowledge of USP, BP, or equivalent pharmacopeial standards and tolerance limits for Pharmaceuticals or Natural Health Products.

Schedule

Monday to Friday, Hybrid - 4 days onsite, 1 day remote.
Location: Scarborough, ON M1S 3R5

Pay: CA$63,000.00-CA$75,000.00 per year

Job Types: Full-time, Contract

Work Location: Hybrid remote in Scarborough, ON M1S 3R5

How to Apply:

Please submit your resume and a cover letter outlining your qualifications and explaining why you are the perfect fit.

Why Join Us

Opportunity to shape the future of CanPrev’s packaging operations during a time of exciting growth.
Work closely with cross-functional teams on high-impact, visible projects.
Be part of a collaborative, purpose-driven team dedicated to improving health and wellness.
Competitive compensation and a comprehensive benefits package.

We thank all applicants for their interest in CanPrev Natural Health; however, only chosen applicants will be contacted. We regret that we are unable to respond to individual inquiries about application status. CanPrev Natural Health is an equal opportunity employer that fosters an inclusive, equitable, and accessible environment. Please notify us if you require accommodation at any time during the recruitment process.

About employer

More about this job

Responsibilities

Lead the quality team and maintain compliance with Natural Health Product regulations and GMP requirements, overseeing documentation, specifications, audits, training, and electronic quality management system activities. Investigate quality issues, manage deviations and change controls, assess risks, and drive corrective actions and continuous improvement with internal teams and external partners.

Requirements

A bachelor's degree in Quality Assurance, Life Science, Food Science, or a related technical field and at least five years of quality leadership experience in natural health products, pharmaceutical, or food manufacturing are required. Candidates should have strong knowledge of GMP regulations, experience maintaining quality documentation and electronic QMS or manufacturing systems, and the ability to lead a quality team.

Skills

Quality Assurance
Quality Management Systems
Good Manufacturing Practices
Regulatory Compliance
Team Leadership
Standard Operating Procedures
Root Cause Analysis
Corrective And Preventive Actions
Deviation Management
Change Control
Risk Assessment
Internal Auditing
Statistical Process Control
Process Validation
Supplier Qualification
Electronic Quality Management Systems

Visa sponsorship

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Keywords

Natural Health Products
Natural Health Product Regulations
NHP GMP
SOR/2003-196
21 CFR Part 111
Good Manufacturing Practices
Quality Management Systems
Electronic Quality Management Systems
Finished Product Specifications
Standard Operating Procedures
Root Cause Investigation
Out Of Specification
Corrective And Preventive Actions
Deviation Management
Quality Agreements
USP
Pharmacopoeial Standards
Change Control
Statistical Process Control
Trend Analysis
Internal Audits
Regulatory Inspections
Risk Assessment
Training Matrix
Process Validation
Stability Studies
Supplier Qualification
Preventive Control Plan
Google Workspace
Manufacturing Software

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