Key Roles and Responsibilities 

• Responsible for day to day chemical analysis of TCM raw/in-process materials and finished products;
• Prepare / review test result and generate test report;
• Assist in development, modification and validation of testing method;
• Conduct calibration and routine maintenance of laboratory instrumentation;
• Assist in generation and review of laboratory documents; &
• Implement requirements of GMP and HOKLAS in daily operation.

Qualifications and Experience   

• Degree Holder of Chemistry / Chemical Technology or Chinese Medicines is a must;
• 3-5 years hands-on experience of Chemical Testing, method development and validations, preferably in Pharmaceutical, Herbal material or Food testing;
• Familiar with instrumental analysis including HPLC, GC-MS, ICP-OES, NIR;
• Knowledge and experience in GMP, ISO17025 is definite advantage;
• Good communication and supervisory skills, self-initiative and a good team player;
• Proficient in written/ spoken English and Chinese;
• Proficient in Microsoft Office; &
• Immediate 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.

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.