Operate all quality related activities in Good Manufacturing Practice ensuring safety and quality of drug manufactured, review process control plan, track drug quality performance, assist drug regulatory registration in Hong Kong and overseas.
Key Roles and Responsibilities
- Operate all quality related activities in Good Manufacturing Practice ensuring safety and quality of drug manufactured
- Review process control plan, drive quality issues to root cause, corrective and preventive actions, track drug quality performance etc.
- Assist drug regulatory registration in Hong Kong and overseas
- Perform ad-hoc tasks as assigned by Supervisor
Qualification and Experience
- Higher Diploma, Associate Degree or Degree holder in science, pharmacy, pharmaceutical or engineering related discipline
- Fresh graduates are welcomed
- Successful candidate is provided great opportunity to join the challenging and rewarding drug manufacturing industry especially during the COVID pandemic
- Possess good communication skill, willingness to learn, attention to details and hardworking attitude
- No experience required but good communication skill, good command of written and spoken English and Chinese are essential