Job Responsibilities

• Responsible for day to day chemical analysis of raw/in-process materials and finished products;
• Prepare / review of test result;
• 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 in daily operation.

Job Requirements

• Degree or above in Chemistry, Pharmacy, Analytical Science or related discipline;
• Minimum 1 year hands on experience chemical testing preferably in pharmaceutical, herbal material or food testing;
• Knowledge on method development and validations will have additional advantage;
• Familiar with instrumental analysis including GC-FID and HPLC;
• Experience with GMP and ISO 17025 is preferred but not essential;
• Self-initiative and a good team player;
• Proficient in written/spoken English and Chinese;
• Proficient in Microsoft Office; &
• Candidate with less relevant experience or lower qualification will be considered as Assistant Quality Control Chemist.

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.