PuraPharm Corporation Limited (HKEx Stock Code: 1498) is a leading Hong Kong-based Chinese medicine company primarily engaged in the research and development, production, marketing and sale of concentrated Chinese Medicine granules (CCMG) products which we market under our brand “Nong’s® (農本方)”....
PuraPharm Corporation Limited (HKEx Stock Code: 1498) is a leading Hong Kong-based Chinese medicine company primarily engaged in the research and development, production, marketing and sale of concentrated Chinese Medicine granules (CCMG) products which we market under our brand “Nong’s® (農本方)”. We are the only CFDA-licensed CCMG product manufacturer in Hong Kong, qualified to issue safety reports recognized by over 70 countries around the world through our in-house CNAS ISO 17025 laboratory, in accordance to the CNAS standards. PuraPharm, the official supplier of CCMG to Hong Kong’s hospitals and healthcare institutions, has been supplying CCMG to the majority of hospitals in Hong Kong since 2004, and is now the leading and the largest supplier of CCMG products in Hong Kong with a market share of 70%.

Regulatory Affairs Executive

Job level Entry
Education Bachelor Degree
Location
Tai Po
Employment type Full Time
Benefits Dental plan, 5-day week, Insurance plan, Medical plan, Performance bonus
Industry Medical services / Pharmaceutical
Job function Legal / Professional Services > Legal & Compliance
Medical Services > Pharmaceutical
Published On 12/01/2019

Job Descriptions

  • To provide executive support in product registration and/or premarket procedures for Hong Kong 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 Hong Kong and overseas market
  • To assist in pre-launch compliance review of marketing materials text specification and artwork, including but not limited to product labels, inserts and promotional materials
  • To renew licenses and maintain license registry for Hong Kong
  • To manage department documentation
  • To assist in any ad hoc tasks as assigned by Supervisor

Job Requirements

  • Higher Diploma or above, preferably in Chinese Medicine, Pharmacy in Chinese Medicine, Pharmacy, Biological Science or other Medical related field
  • Experience in regulatory affairs or pharmaceutical industry is preferred but not essential
  • 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 more relevant experience would be considered as Senior Regulatory Affairs Executive.

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 www.purapharm.com. 

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.