This position is a core and critical role within the GLP organization, primarily responsible for overseeing and leading laboratory scientific research management. It involves spearheading the implementation of comprehensive process control for all non-clinical research projects, ensuring that all ongoing projects strictly adhere to the Good Laboratory Practice (GLP) standards, as well as relevant national laws, regulations, and technical guidelines. The incumbent must possess a solid theoretical foundation in non-clinical drug research, a systematic industry knowledge framework, along with extensive hands-on experience in non-clinical research and project management, enabling effective support for the standardized, compliant, and regulated operation of laboratory scientific research