Responsibilities

• Support the development, implementation, maintenance and continual improvement of the pharmaceutical quality management system to ensure the compliance with relevant ISO and GMP standards
• Responsible for document (SOP, Specification, etc) preparation and review
• Coordinate with internal parties to exercise document control and maintain operational records over the management system documentation
• Assist in handling product registration
• Execute and follow up in external and internal audit programs
• Assist in other ad-hoc tasks as assigned
• Work location: Tseung Kwan O Industrial Estate

Qualifications

• Higher Diploma or above in sciences, pharmaceutical or related discipline
• 3 to 5 years of working experience in Quality Assurance, preferably in pharmaceutical industry
• Experience in interacting with health authorities and industry associations
• Experience in ISO9001 and GMP quality management
• Good command of written and spoken English and Chinese
• Proficient in MS Office applications (Excel, Word & PowerPoint) and Chinese Word Processing

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