Support biopharmaceutical quality systems through validation, qualification, and technical documentation as a Quality Engineer at STEMCELL Technologies.

This Quality Engineer role supports full project phase execution within a life science research organization. You will work across Manufacturing, Quality Control, Process Development, and Instrumentation on commissioning, qualification, validation, and hand-over. The position also includes PPQ manufacturing support and quality investigations.

Key Responsibilities:

- Generate master plans, schedules, risk assessments, and reports
- Support PPQ conformance lot manufacturing and increased testing
- Perform non-conformance and CAPA investigations when needed
- Review and coordinate validation execution documentation




- Train employees on applicable quality standards

Requirements:

- Bachelor’s degree in Biomedical Engineering or equivalent
- Two to six years’ experience in validation work
- Utilities, facilities, equipment, and controlled chamber experience
- Software assurance and Continued Monitoring familiarity
- Excellent technical report writing and document analysis abilities

Use validation documentation, PPQ support, and CAPA investigation skills to strengthen biopharmaceutical quality assurance at STEMCELL.

📌 Biopharmaceutical Validation Quality Engineer (Burnaby)
🏢 Job type:
📍 Burnaby