This position is responsible for managing the execution of of assays, process, methods, procedures, pre-validation, or validations. Most work will require strict adherence to compliance with good scientific principle, and considerations of future compliance with current Good Manufacturing Practices (cGMP), and relevant SFDA and other international regulatory regulations as needed, and Standard Operating Procedures (SOPs). Under direct supervision from the department head, the position runs, manages and schedules the performance of testing, and studies, ensuring completion of records, including but not limiting to, batch records and other required documentation and laboratory maintenance duties according to SOPs.