Manage pharmacy-related stages in drug R&D and production; track project progress and resolve issues.
Ensure the quality of project documentation; organize and review records; participate in the writing and review of product application materials.
Responsible for process handover, pilot trials, and process validation before submission; address technical problems related to product manufacturing.
Supervise CRO & CDMO partners in research implementation; identify technical challenges in process development, supporting optimization and production scaling.
Coordinate interdepartmental tasks related to pharmacy.

Bachelor’s degree or higher in Chemistry, Biology, Pharmacy, or a related field.
Over 5 years of experience in drug synthesis or formulation development; expertise in innovative drug R&D and CRO & CDMO management is preferred.
Strong problem-solving skills, literature review proficiency, and ability to write technical documents in English.
Excellent communication, execution, learning abilities, and teamwork spirit.
Proficient in written English.