Responsibilities:

• Implement and maintain PQS in a PIC/S GMP pharmaceutical plant
• Supervise routine QA department functions, including but not limited to line clearance, technology transfer, internal and external inspections, change control & risk assessment, product returns, complaints and recalls
• Perform annual PQR for finished products
• Responsible for documentation and execution of various qualification & validation activities for equipment, processes, facilities & utilities, i.e. URS, DQ/IQ/OQ/PQ, CV/PV/CSV, etc.
• Ad hoc tasks as assigned by management

Requirements:

• Degree holder or above in Pharmacy, Chemistry, Biology, Life Science or related science disciplines
• At least 3 year experience in QA department of GMP certified pharmaceutical industry
• With supervisory experience would be an advantage
• Self-motivated, well-organized and good communication & coordinating skills
• Proficient in spoken and written English and Chinese
• Proficiency in computer application such as Excel, Word
• Applicant with less experience will be considered officer position

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.)