Responsibilities:

• Prepare specifications, SOPs and other GMP controlled documents.

• Maintain and improve product quality, communicate and coordinate with internal parties on quality issues.

• Support and facilitate audits and regulatory inspection.

• Participate in validation activities and assist in preparing validation protocols and reports.

• Prepare regular reports and participate in ad hoc projects and other assigned duties.

Requirements:

• Higher diploma or above in Chemistry, Chinese Medicine or related disciplines.

• At least 3 years working experience in quality assurance of pharmaceutical or related industries.

• With good understanding on GMP / ISO 9000.

• Familiar with Microsoft Office applications.

• Independent, enthusiastic with good communication skills and ability to interact with employees at all levels.

• Good command of spoken and written English and Chinese.
  
  

We offer 5-day work week, free lunch, shuttle bus, double pay, discretionary bonus and comprehensive benefits to the right candidate. Please apply in confidence with full resume, listing present and expected salary to by clicking “Apply Now”.

(Data collected will be treated in strict confidence and only be used for recruitment purpose.)