The Quality Technical and Validation Lead ensures GxP compliance in validating and qualifying processes, equipment, facilities, utilities, software, and systems across manufacturing and analytical areas
Job Summary
The Quality Technical and Validation Lead ensures GxP compliance in validating and qualifying processes, equipment, facilities, utilities, software, and systems across manufacturing and analytical areas.
Responsibilities include maintaining robust change management for process, equipment, and computer system validation lifecycle activities, applying Quality by Design (QbD) principles, and ensuring adherence to GSK and regulatory standards.
This role offers an on-site (weekly 5 days) working model at Ware, Hertfordshire, UK.
Matching Summary
The Quality Technical and Validation Lead ensures GxP compliance in validating and qualifying processes, equipment, facilities, utilities, software, and systems across manufacturing and analytical areas.
Skills & Requirements
Must-have
GxP compliance
validation and qualification
change management
Quality by Design principles
regulatory standards adherence
new product introduction oversight
Nice-to-have
agile and culturally adaptable approaches
collaboration and innovation
problem solving and troubleshooting
site business drivers knowledge
Key Requirements
Bachelor’s degree in Chemistry, Biology, engineering, or related
Pharmaceutical industry experience
Process Lifecycle Management experience
Quality operations experience
Analytical equipment and method validation experience