Job Purpose
This position ensures pharmaceutical products registration in Korea market is timely and compliant with GSK and MFDS regulatory requirements in terms of Specification and Test methods.
Coordinates and supports analytical test method set up/change associated with global/local changes including New Product Introduction and Existing Products.
Third Party Laboratory Management for Release testing and Analytical Method Transfer
Reagent management for Analytical Method Transfer
National Inspection technical support in terms of Specification and Test Methods
This position is responsible for providing the contribution to the compliance and continuous improvement of the Quality Management System, especially for lab management system.
Develops and improves LOC quality systems in line with the strategies and policies.
Responsible to implement and monitor LOC Quality strategy.
Key Re...