Standardize production operations: Strictly follow standard operating procedures (SOP) to operate production equipment, accurately execute pre-processing, extraction, preparation, mixing or inner packaging of Chinese medicine, and immediately and accurately fill in batch production records.

Quality process control: Responsible for carrying out online quality control point checks during the production process, actively identifying and immediately reporting any production deviations, abnormalities or potential risks, and ensuring that all operations comply with the Hong Kong GMP and the TCM Ordinance's regulatory requirements.

Material and environmental management: Responsible for the verification, transfer and cleaning of materials before and after production, strictly maintain a clean environment according to the regulations, and execute various sanitation and disinfection procedures to effectively prevent pollution and cross-contamination.

Safety and team collaboration: Strictly follow environmental, health and safety (EHS) procedures, assist with daily equipment inspections and basic maintenance; actively collaborate with QA, QC and engineering departments to support on-site work for internal and external as well as official audits.

Education and experience: Secondary five education or above, must have at least one year of GMP standardized pharmaceutical factory production line actual operation experience; those with Chinese herbal extraction, processing or pharmaceutical packaging related experience will be given priority.

Regulations and quality awareness: Understand the Hong Kong Chinese Medicine Ordinance and GMP basic guidelines, master core quality requirements such as cleaning and material verification, and have basic production deviation identification and reporting awareness.