Authorized Person (Registered Pharmacist)
Ref. Code. n0423



  • Batch release of finished products.
  • Ensure every released batch is compliant to relevant GMP standards and Marketing Authorizations.
  • Supervise manufacturing, quality control and quality assurance activities for compliance to relevant GMP standards.
  • Participate in validation, deviations, change controls, CAPA and quality risk management activities.
  • Ensure self inspections are carried out according to established procedures. 
  • Other duties assigned by management.
  • Occasional travel may be required.




  • Registered Pharmacist in Hong Kong with valid Practicing Certificate issued by the Pharmacy and Poisons Board of Hong Kong.
  • Minimum 3 years related work experience in GMP pharmaceutical manufacturing or quality control.
  • Familiarity with sterile products manufacturing and/or PIC/S GMP would be an advantage.
  • Good command of spoken and written English and Chinese; Putonghua is an advantage.
  • Immediately available is preferable.


Interested candidates, please forward your resume in WORD format to [email protected] quoting reference 'n0423' in the subject line


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