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.

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