Key Roles and Responsibilities 

• To prepare and review GMP document;
• To maintain the GMP documentation system;
• To assist in executing the Quality Management System;
• To implement QA daily operation in the manufacturing site; &
• Other ad hoc projects as assigned.

Qualifications and Experience    

• Degree holder in Chemistry, Quality Management, Food Sciences or other Sciences related disciplines;
• 3 years or above relevant working experience in the Pharmaceutical or Food manufacturing industry is highly preferred;
• Knowledge in Quality Assurance System in pharmaceutical/food/laboratory will be an advantage;
• Good command of written and spoken both in English and Chinese;
• Able and willing to work on Saturday or Sunday (5 days work per week); &
• Candidate with less experience will be considered as Assistant Quality Assurance Officer.

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.

Europharm Laboratoires is one of the leading GMP (Good Manufacturing Practice) pharmaceutical manufacturing Company located in Tai Po Industrial Estate. We are seeking high caliber person to fill in the following post.