Key Roles and Responsibilities

• To support in developing, implementing and maintaining the documentation and Quality Assurance system of the company, including the standard operating procedures (SOPs); &
• Has GMP knowledge is an advantage.

Qualifications and Experience   

• Higher Diploma / Associate Degree or equivalent in Chinese Pharmaceutical Studies / Chinese Medicines related discipline;
• One-year relevant experience is preferred but Fresh Graduate is also welcome;
• Attention to details, hard-working and being able to work under pressure;
• Strong communication skill, good command of English and Chinese; &
• Immediate Available is 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.