Apply Quality Assurance expertise to protect product and service quality at Canadian Blood Services, with at least 40% on-site presence. Use GMP knowledge, analysis, and communication across a temporary full-time assignment.

As a temporary full time Quality Assurance Associate, you will provide organizational assurance for safety, quality, identity, purity, potency, and accessibility requirements. You will apply Quality Management System principles across controlled processes, deviations, audits, validation, and CAPA. The position requires post-secondary education or equivalent experience, plus substantial quality management experience.

Key Responsibilities:

- Maintain controlled processes and apply Quality Management System principles
- Analyze data and conduct root cause investigations
- Lead internal and external audit activities




- Coach staff on GMP and documentation practices
- Identify recurring issues, gaps, risks, and improvement recommendations

Requirements:

- Relevant post-secondary education or equivalent experience
- Five-plus years in Quality Management and Continuous Improvement
- Three-plus years in GMP testing or diagnostics quality assurance preferred
- Knowledge of Health Canada, CSA, and AABB standards
- Quality Management Systems and Microsoft Office technical skills

Bring GMP, analytical, audit, and quality systems expertise to Canadian Blood Services while supporting compliant products and services.

📌 Quality Assurance Associate GMP Compliance (St. John's)
🏢 Canadian Blood Services
📍 St. John's