Responsibilities:

• To assist in developing, implementing and maintaining the documentation system, including the Standard Operating Procedures (SOPs) and other production documents
• To ensure and maintain the adequate and accurate records for controlling and monitoring conformity to specified GMP and statutory requirements
• To assist monitor warehouse storage and daily operation
• To assist monitor the production process according to the production plan
• To perform the daily operation and ad-hoc functions of Production Department
• To assist the head of production to monitor the daily production workflow

Qualifications:

• Higher Diploma holder or above 
• Relevant experience in GMP pharmaceutical manufacturing is preferred
• Familiar with MS office and Chinese word processing
• Hardworking, initiative, self-motivated and fast learner
• Able to work under pressure and willing to work overtime
• Good interpersonal skill and communication skill