Key Roles and Responsibilities 

• Provide clerical supports to the Quality Control ("QC") Department;
• Handle general administrative works; 
• Organize QC Laboratory schedule;
• Perform routine check in the QC Department to ensure GMP implementation and compliance; &
• Assist in other ad-hoc duties as required.

Qualifications and Experience    

• Form 5 or above;
• At least 1 - 2 years clerical experience;
• Good command of Chinese and English;
• Good in MS Office application and Chinese Word Processing;
• Pleasant, hardworking and willing to learn; &
• IMMEDIATELY AVAILABLE is highly preferred. 

How to Apply

You are invited to send in your application and CV stating the position you are applying for together with your current and expected salary, either by Clicking "Apply Now" or Mail to 12-14 Dai Wang Street, Tai Po Industrial Estate, Tai Po, NT. 

Europharm Laboratoires Company Limited is an equal opportunities employer. The information provided will be treated in strict confidence and used only for consideration of application for relevant / similar post(s).  All personal data of unsuccessful applicants will be destroyed within 6 months.