Join a global quality assurance team dedicated to ensuring consistent execution of quality standards and regulatory compliance in a GMP environment
Job Summary
Join a global quality assurance team dedicated to ensuring consistent execution of quality standards and regulatory compliance in a GMP environment.
You will be responsible for writing procedures, maintaining the QMS system, and overseeing change control and CAPA processes to ensure product quality.
The role involves executing self-inspections, coordinating audit readiness activities, and supporting site management reviews to drive continuous improvement.
Matching Summary
Join a global quality assurance team dedicated to ensuring consistent execution of quality standards and regulatory compliance in a GMP environment.
Skills & Requirements
Must-have
Good Manufacturing Practices GMP compliance
SOP writing and review
Change control system maintenance
CAPA system management
Document and record management
GMP training system oversight
Self-inspection program execution
Nice-to-have
Track Wise experience
Biologics and aseptic training
Site data integrity management
Supplier management oversight
Cross-functional collaboration skills
Quality risk management tools
Continuous improvement mindset
Key Requirements
Bachelor's Degree in Life Sciences or Engineering
1-3 years relevant Quality experience in pharmaceuticals
Knowledge of cGMP and Regulatory Compliance
Experience with Track Wise is an asset
Fresh graduates with relevant qualifications considered