(a) To participate in the research of medical device technologies and regulatory requirements; (b) To assist in the development and implementation of post-marketing vigilance and surveillance system; (c) To scrutinize applications for listing of medical devices and traders; (d) To assist in investigation of medical devices-related adverse incidents; (e) To support the design, implementation and evaluation of health promotion projects; and (f) To liaise with the medical device industry, government departments and other authorities on medical device control. [Remark: May be required to work shift and irregular hours when necessary.]

Candidates should - (a) have a Master degree in Microbiology, Biochemistry, Chemistry, Biomedical Sciences, Biomedical Engineering, Medical Engineering, Medical Physics or related disciplines from a Hong Kong university, or equivalent; (b) 2 years of post-qualification experience in research, development, regulatory affairs or marketing related to medical devices is preferred (Note (1)); (c) have met the language proficiency requirements of Level 2 or above in Chinese Language and English Language in the Hong Kong Certificate of Education Examination (HKCEE) or Hong Kong Diploma of Secondary Education Examination (HKDSEE) or equivalent (Note (2)); (d) be able to speak fluent Cantonese and English; and (e) have sound knowledge and experience in using computer software for word processing, presentation, database and information management. [Remark: Candidates may be invited to attend a written test.]