Assistant Regulatory Affairs Manager / Regulatory Affairs Manager
Purapharm Corporation LimitedTai poUpdate time: December 3,2019
Job Description

Job Descriptions

  • To plan, implement and monitor projects on product registration and /or premarket procedures for HK and overseas markets
  • To supervise and execute product registration and/or premarket procedures for HK and overseas markets, including but not limited to preparation and submission of registration dossier and maintenance of registration database in a timely manner
  • To assist in handling communications with regulatory bodies in HK and overseas market
  • To assist in pre-launch compliance review of marketing materials text specification and artwork, including but not limited to labeling and promotional materials
  • To renew licenses and maintain license registry for HK
  • To manage department documentation
  • To assist in any ad hoc tasks as assigned by Manager

Job Requirements

  • Higher Diploma or above, preferably degree in Chinese Medicine, Pharmacy in Chinese Medicine, Pharmacy, Biological Science or other Medical related field
  • Minimum 2 years solid experience in regulatory affairs or pharmaceutical industry, preferably in proprietary Chinese medicine
  • Excellent communication & interpersonal skills
  • Able to work independently under pressure with attention to details, well-organized and responsible
  • Excellent proficiency in spoken and written English and Chinese
  • Candidates with less experience will be considered as Assistant Regulatory Affairs Manager

Working Location: Hong Kong Science Park, Tai Po, N.T.

We offer 5-day working week and an attractive remuneration package. Interest parties please click “”. For company details, please visit 

Our company is an equal opportunity employer. All personal data collected will be used for recruitment purpose only, while the personal data of the unsuccessful applicants will be destroyed within 6 months after the recruitment process.

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