Duties

• To scrutinize applications on listing of medical devices and listing of traders including local manufacturers, importers and distributors;
• To conduct literature review to facilitate the development and drafting of internal enforcement guidelines and procedures;
• To assist in coordinating public engagement with relevant stakeholders and othe publicity matters to introduce the ultimate statutory regulation of medical devices and licensing requirements;
• To assist in ad hoc projects;
• To carry out any other duties as assigned by supervisors/senior staff;

Requirements of Staff

• Be a permanent resident of the Hong Kong Special Administrative Region;
• Have a Bachelor honours degree in Biochemistry, Biomedical Sciences, Chemistry,
• Microbiology or Biomedical Engineering from a Hong Kong university, or equivalent;
• Have 2 years’ of relevant post-qualification working experience in the fields related to research development, regulatory affairs or marketing related to medical devices;
• Preferably have relevant working experience in the Government or public sector;
• Have good command of both written and spoken English and Chinese and have met the language proficiency requirements of Level 2 in the two language papers (Use of Chinese and Use of English) in the Common Recruitment Examination (CRE) or equivalent
• Have strong analytical, organization, co-ordination, communication and interpersonal skills;
• Have strong skills in project management; and
• Be proficient in PC skills in particular the application of MS Office such as MS Word, Excel and PowerPoint.