QA Analyst

About Resolute

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 Analystin Brantford, ON (Onsite). This is a contract role.

Responsibilities:

• Prepare, review, and issue quality documentation, including batch records, packaging records, Certificates of Analysis (COAs), and product release documents.
  
• Ensure compliance with cGMP, GLP, FDA, Health Canada, and internal quality standards through document reviews, internal audits, and regulatory inspections.
  
• Coordinate Change Control, CAPA, deviation investigations, OOS/OOT investigations, and customer/vendor complaints, ensuring timely follow-up and closure.
  
• Develop, review, and maintain SOPs, controlled documents, master indexes, and quality records to support effective document control.
  
• Perform in-process inspections, production line clearances, and technical document reviews, including raw materials, finished products, stability, and validation records.
  

• Support product launches, customer and label revisions, and preparation of Annual Product Quality Reports (APQRs).
  

Qualifications:

• Bachelor’sdegreeinChemistry,Microbiology,orarelatedscientificdisciplinefromarecognizedaccreditedinstitution.
  
• Minimum 2 years of experience in Quality Assurance, Quality Control, and Validation within a pharmaceutical manufacturing cGMP environment.
  
• Strong knowledge of applicable regulatory and industry standards, particularly cGMP and GLP requirements.
  
• Ability to organize effectively, prioritize, and manage multiple tasks in a fast-paced environment.
  
• Valid WHMIS (Workplace Hazardous Materials Information System) training.
  
• Excellent organizational and time-management skills with strong attention to detail.
  
• Strong interpersonal skills with the ability to collaborate effectively with manufacturing personnel, administrative teams, and external contacts.
  

Note: The annual salary range is $50,000–$60,000, depending on skills and experience relevant to the role.