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Responsibilities: Implement and maintain PIC/S GMP documentation system in a GMP pharmaceutical plant Support routine QA department functions, including but not limited to line clearance, training program, self-inspection, change control, product returns, complaints and recalls Assist in managing the document control system, such as generating, filing and archiving of controlled documents Assist in preparing documents and execution of various qualification & validation activities for equipment, facilities & utilities, i.e. URS, DQ/IQ/OQ/PQ, CV/PV, etc. Handle ad hoc tasks as assigned Requirements: Diploma in Pharmacy, Chemistry, Biochemistry, Life Science or related disciplines 1 year of experience in QA department of GMP certified pharmaceutical industry Proficient in MS Office Good command of spoken and written English and Chinese Interested parties please send full resume with present and expected salary to Human Resources Department by clicking "APPLY NOW". (Information provided will be treated in strict confidence and will only be used for recruitment-related purposes.)