RESPONSIBILITIES

• Maintains GMP Documentation System
• Handle staff training program
• Handle Annual Product Reviews
• Draft and Review SOPs and GMP related documents
• Documentation review and follow-up for registered products
• Conduct on-site inspection on the GMP related departments
• Handle other quality matters

REQUIREMENTS

• Higher Diploma or above
• At least 2 years of experience in the Pharmaceutical Industry
• Knowledge of PIC/S GMP requirements
• MS office and Chinese word typing
• Willing to learn and is responsible
• Able to communicate well and work with others
• Strong coordination and time management when dealing with multiple tasks
• Good command of both written and spoken Chinese and English

Interested parties please send CV and expected salary by clicking 立即申請 for interview.

Data collected will be used for recruitment purpose only.