Job description and responsibilities: 

• Responsible to perform testing of the material (including starting materials, packaging materials, intermediate product) and products referring to the SOPs.
• Responsible to operate laboratory instrument.
• Responsible to perform instrument calibration and maintenance.
• Responsible to carryout validation of test method.
• Responsible to perform RO water and Environmental monitoring.
• Responsible to prepare QC inventory control such as chemicals & working standard receiving and storage.
• To perform any quality control duties as assigned

 Job requirements

• Higher Diploma, Associate Degree or Degree holder in Biology, Chemistry, Pharmaceutical Studies or any related discipline
• More than 1 year working experience of a GMP pharmaceutical industry is preferred.
• Familiar with testing instrumental analysis in HPLC & GC is preferred.
• Hardworking, initiative, self-motivated and fast learner
• Good problem solving skills
• Good command in both written and spoken Cantonese and English
• Proficiency in computer application such as MS Office and Chinese word processing
• Candidate with less experience or qualification will be considered as QC Assistant