Lead GMP compliance and validation activities as a QA Compliance Analyst at an onsite pharmaceutical manufacturing facility in Brantford, Ontario. Apply quality expertise across regulated operations.
This contract role supports production demands through Resolute Workforce Solutions, a Brevitas Consulting subsidiary. You will manage quality systems, analytical methods, audits, deviations, CAPA, and validation activities. The position also oversees QA and QC operations while coordinating with Production, customers, and other departments.
Key Responsibilities: Maintain procedures, analytical methods, and compliant quality systems
Oversee QA and QC operations, training, assignments, and budgets
Manage Change Control, Deviations, CAPA, and supplier audits
Coordinate product release, recalls, complaints, and document approvals




Prepare regulatory audit responses and maintain compliance programs
Requirements: Bachelor’s degree in Chemistry, Microbiology, or related science
Minimum seven years in pharmaceutical QA, QC, and Validation
Knowledge of cGMP, GMP, GLP, and validation requirements
Robust organization, problem-solving, communication, and judgment skills
MS Office and Smartsheet proficiency preferred; quality certification advantageous
Use pharmaceutical QA, validation, audit, and CAPA expertise to support compliant manufacturing operations onsite in Brantford, Ontario.

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📌 Pharmaceutical QA Compliance Analyst (Ontario)
🏢 Resolute Workforce Solutions
📍 Ontario