Key Roles and Responsibilities

• Provide assistance in preparing validation documents, collecting data and writing reports;
• Support process optimization and technology transmits;
• Perform process and equipment validation tasks;
• Contribute in enhancing product quality; &
• Maintain re-validation list and files.

Qualifications and Experience   

• Degree in Chemistry / Chemical Engineering / Industrial and System Engineering  or equivalents;
• Good computer skills as well as be able to analysis and determine the relevance of data collected;
• Good communication skills both verbal and written are essential as routine reports;
• Experience in Pharmaceutical / GMP environment added advantage;
• Demonstrated ability to work well with others and as a team member;
• Strong communication skill;
• Good command of written English and Chinese; &
• 1-3 years relevant working experience preferred but fresh graduates are also welcome.

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. 

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.