Requirements:

• Bachelor degree or above in pharmacy or pharmaceutical sciences
• Familiar with PIC/s GMP and have relevant experience in pharmaceutical manufacturing is value-added
• Fluent spoken and written English, Chinese is an advantage but not essential
• Independent, hard working, detailed minded, organized, self motivated, good communication skill

Key Responsibilities:

• Participate in quality assurance monitoring program, validation and qualification work of facilities, equipment, GMP related documentation preparation, review and control in order to ensure compliance with PIC/s GMP standards
• Learn and operate production equipment
• Involve in training
• Handle ad hoc projects as assigned

Work Location: Tai Po