QA/QC Technician

Brevitas; Brantford; On-site; CAD 30,000 - 39,000; Full time

Job summary

Resolute Workforce Solutions, a staff augmentation subsidiary of Brevitas Consulting Inc., is seeking a QA/QC Technician for a Brantford, ON onsite role at a pharmaceutical manufacturing facility. The position offers a potential extension to 1 year and requires strong GMP/QC experience.

Responsibilities include quality inspections, batch review, document control, OOS/OOT investigations, and maintaining GMP compliance while working rotating shifts with health and safety adherence.

Qualifications

• Minimum college diploma in Chemistry, Pharmaceutical Sciences, or a related field.
• 2-3 years of experience in Quality Control/Quality Assurance within a GMP-regulated environment.
• Experience in Quality Control/Quality Assurance within a GMP-regulated environment.
• Hands-on experience performing physical and chemical testing in a GLP laboratory.
• Knowledge of applicable cGMP, GLP, regulatory, and industry standards.
• Strong organizational skills with the ability to manage multiple priorities and tasks.
• WHMIS training and knowledge of workplace safety requirements.
• Good judgment and problem-solving skills when evaluating test results, identifying discrepancies, and determining appropriate modifications or corrective actions.
• Availability to work rotating shifts, including days, evenings, nights, and weekends.
• Overtime may be required based on production needs and must be approved by Management.

Responsibilities

• Perform quality inspections, line clearances, and testing/release of packaging components and in-process bulk products in accordance with approved manufacturing and packaging records.
• Review batch records, packaging orders, QC test results, raw materials, finished products, stability, and validation documentation.
• Assist with document control activities, including issuing, filing, and archiving batch records, packaging records, SOPs, and other controlled documents.
• Support laboratory operations and participate in investigations and follow-up of non-conformances, Out-of-Specification (OOS), and Out-of-Trend (OOT) results.
• Assist in maintaining quality assurance procedures, evaluating production processes, and recommending improvements to ensure GMP and quality compliance.
• Follow all applicable health and safety requirements, use required PPE, remain flexible to work different shifts, and perform other duties as assigned.

Skills

Quality control

Quality assurance

GLP laboratory experience

cGMP/GLP knowledge

Problem solving

Organizational skills

Education

College diploma in Chemistry / Pharmaceutical Sciences

Tools

WHMIS training

Job description

Brantford, Canada | Posted on 11/07/2026

Resolute Workforce Solutions, a staff augmentation subsidiary of Brevitas Consulting Inc., provides qualified professionals to support the workforce requirements of organizations in the pharmaceutical and life sciences sectors.

We have been retained by a pharmaceutical manufacturing company to support its increased production demands through the provision of qualified resources at its manufacturing facility in Brantford, Ontario. All positions associated with this engagement are site-based and require personnel to work on-site. Please review the site location and associated logistics, including commuting arrangements, accessibility, and any site-specific requirements, when considering these opportunities.

Role Overview

We are looking for a highly motivated and energetic professional to join our team as a QA/QC Technician in Brantford,ON (Onsite). This role has a significant potential to extend to 1 year.

Responsibilities

• Perform quality inspections, line clearances, and testing/release of packaging components and in-process bulk products in accordance with approved manufacturing and packaging records.
• Review batch records, packaging orders, QC test results, raw materials, finished products, stability, and validation documentation.
• Assist with document control activities, including issuing, filing, and archiving batch records, packaging records, SOPs, and other controlled documents.
• Support laboratory operations and participate in investigations and follow-up of non-conformances, Out-of-Specification (OOS), and Out-of-Trend (OOT) results.
• Assist in maintaining quality assurance procedures, evaluating production processes, and recommending improvements to ensure GMP and quality compliance.
• Follow all applicable health and safety requirements, use required PPE, remain flexible to work different shifts, and perform other duties as assigned.

Qualifications

• Minimum college diploma in Chemistry, Pharmaceutical Sciences, or a related field.
• 2-3 years of experience in Quality Control/Quality Assurance within a GMP-regulated environment.
• Experience in Quality Control/Quality Assurance within a GMP-regulated environment.
• Hands-on experience performing physical and chemical testing in a GLP laboratory.
• Knowledge of applicable cGMP, GLP, regulatory, and industry standards.
• Strong organizational skills with the ability to manage multiple priorities and tasks.
• WHMIS training and knowledge of workplace safety requirements.
• Good judgment and problem-solving skills when evaluating test results, identifying discrepancies, and determining appropriate modifications or corrective actions.
• Availability to work rotating shifts, including days, evenings, nights, and weekends.
• Overtime may be required based on production needs and must be approved by Management.

Note

Salary ranges $22–$28 per hour , depending on skills and experience relevant to the role.

We thank all applicants in advance; however, we will only contact the candidates whose qualifications match closely to the job requirements.

We welcome and encourage applications from people with disabilities. Accommodations are available on request for candidates taking part in all aspects of the selection process.