STEMCELL Technologies seeks a Quality Engineer skilled in cGMP validation, technical documentation, and qualification across regulated life science operations.

This Quality Engineer supports processes, analytical methods, and equipment lifecycle verification within risk-based validation programs. You will create master plans, schedules, risk assessments, protocols, and summary reports. The position collaborates across Manufacturing, Quality Control, Process Development, and Instrumentation during project phase execution.

Key Responsibilities:
Prepare master plans, schedules, risk assessments, and protocols
Coordinate commissioning, qualification, validation, and hand-over execution
Support PPQ manufacturing with increased testing activities
Establish quality procedures,



processes, and policies
Train and advise employees on quality standards

Requirements:
Bachelor’s degree in Biomedical Engineering or equivalent
Two to six years in a validation job
Qualification experience in manufacturing and quality control laboratories
Experience with temperature chamber mapping and monitoring
Excellent technical report writing and document analysis abilities

Bring cGMP validation, qualification, and technical reporting experience to cooperative project execution at STEMCELL Technologies.

📌 Validation Quality Engineer Cgmp Burnaby
🏢 STEMCELL Technologies
📍 Burnaby