(a) 協助研究和檢討香港現行的中藥規管制度；
(b) 協助就規管中藥方面與內地和海外藥品規管當局聯絡和舉行會議；
(c) 負責中成藥註冊的審核及向下屬提供相關的專業支援；
(d) 協助就«中醫藥條例»附表1和2的任何修訂編寫報告；
(e) 協助就中成藥有關毒性，穩定性和品質標準等編寫報告；
(f) 鑒別中藥材及檢查其品質，及向下屬提供相關的專業支援；
(g) 協助為執行中藥規管的人員制定和提供適當的培訓；及
(h) 負責上司指派的其他職責。

[備註：可能須輪班及不定時工作。]

(a) To assist in studying and reviewing Hong Kong existing regulatory system of Chinese medicines;
(b) To assist in liaison and holding of meetings with Mainland and overseas drug regulatory authorities for the control of Chinese medicines;
(c) To be responsible for assessment of registration of proprietary Chinese medicines and provide professional support to subordinates on related matters;
(d) To assist in preparing reports regarding any amendments to Schedules 1 and 2 of the Chinese Medicine Ordinance;
(e) To assist in preparing reports regarding toxicity, stability, quality specification, etc of the proprietary Chinese medicines;
(f) To identify Chinese herbal medicines and assess their quality, and provide relevant professional support to subordinates;
(g) To assist in planning and providing necessary training to the professional staff for the enforcement of the regulations on Chinese medicines; and
(h) To carry out any other duties as assigned by seniors.

[Remark: May be required to work shift and irregular hours.]