QA/QC Technician

Resolute Workforce Solutions; Brantford; On-site; CAD 30,000 - 39,000; Full time

Job summary

Resolute Workforce Solutions is seeking a QA/QC Technician for a Brantford, ON site-based role within a pharmaceutical manufacturing environment. The position is onsite with potential to extend and requires GMP-compliant QA/QC activity, documentation control, and lab testing.

Responsibilities include inspections, batch record review, investigation of OOS/OOT, and adherence to cGMP/GLP standards. Compensation ranges from $22–$28 per hour depending on experience, with rotating shifts and

Qualifications

• Minimum college diploma in Chemistry, Pharmaceutical Sciences, or related field.
• 2–3 years’ experience in QC/QA within a GMP environment.
• Hands-on testing in a GLP laboratory.
• Knowledge of cGMP, GLP, and regulatory standards.
• WHMIS training and workplace safety knowledge.

Responsibilities

• Perform quality inspections, line clearances, and testing/release of packaging components and in-process bulk products.
• Review batch records, packaging orders, QC results, materials, finished products, stability, and validation docs.
• Assist with document control activities including issuing and archiving batch records, SOPs, and controlled documents.
• Support lab operations and investigations of non-conformances, OOS, and OOT results.
• Assist in maintaining QA procedures and recommending process improvements to ensure GMP compliance.
• Follow health and safety requirements, use PPE, and work rotating shifts.

Skills

Quality Control/Quality Assurance

GMP knowledge

GLP knowledge

Organizational skills

Problem-solving

WHMIS training

Shift work

Education

College diploma in Chemistry or Pharmaceutical Sciences

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 experience.

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.