QA/QC Technician

About Resolute

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.

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.

• 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.
  
  

• 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.