Quality Engineer Validation Specialist

3 days ago

Vancouver BC, Greater Vancouver Regional District, BC; British Columbia, Canada STICA STEMCELL Technologies Canada Inc. Full-time
Risk-based validation expertise meets cGMP quality engineering at STEMCELL Technologies in Vancouver, supporting processes, methods, and equipment verification. As a Quality Engineer, you will support lifecycle verification across commissioning, qualification, validation, and project hand-over activities. You will collaborate with Manufacturing, Quality Control, Process Development, and Instrumentation teams. Your work includes risk assessments, protocols, schedules, master plans, and summary reports.

Key Responsibilities
Develop metrics for process effectiveness and improvement progress Support PPQ conformance lot manufacturing and increased testing Perform non-conformance and CAPA investigations when needed Prepare and coordinate validation, commissioning, and qualification documentation Coach employees on applicable quality standards and procedures

Requirements:
Bachelor’s degree in Biomedical Engineering or equivalent Two to six years of validation experience Familiarity with risk management, ISO 14971, and cGMP Experience qualifying utilities, facilities, equipment, and controlled temperature chambers Strong technical report writing, analysis, project, and time management skills Apply validation, risk management, and technical documentation expertise to quality assurance at STEMCELL Technologies in Vancouver. #J-18808-Ljbffr