Duties include:

1. Standardize production operations: Strictly follow the standard operating procedures (SOP) to operate production equipment, accurately execute the specified processes of Chinese medicine such as pretreatment, extraction, preparation, mixing or internal packaging, and fill out batch production records in real time and accurately.

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

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

4. 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 and official audits.

Position requirements

1. Education and experience: Secondary Five or above, must have at least one year of GMP-compliant pharmaceutical factory production line actual operation experience; those with Chinese herbal extraction, preparation or pharmaceutical packaging related experience will be given priority.

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

Other information