Key Roles and Responsibilities

Assisting the Production Controller for the following duties:-

• Preparing documents (e.g. MBPR & SOPs) for the production dept;
• Organize production schedule;
• Supervise and monitor day-to-day running of the production operation;
• Coordinate with other departments on production schedule and validation arrangement;
• Train the new staff in the Production Department; &
• Perform routine check in the Production Department to ensure GMP implementation and compliance.

Qualifications and Experience    

• Higher Diploma / Associate Degree or Degree in Pharmaceutical Sciences or any related Sciences studies;
• 1 year of GMP experience in Manufacturing or Production of Pharmaceutical Industry at least is highly preferred;
• Attention to details, hard-working and being able to work under pressure;
• Decisive, independent with strong communication and management skills;
• Good command of both spoken and written English and Chinese.
• Proficient in MS Office application (Excel, Word & PowerPoint) and Chinese Word Processing; &
• Immediate available is highly preferable.

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.