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Job ref no.: CT3115399-01#0022
BRIGHT FUTURE PHARMACEUTICAL LABORATORY LTD

Regulatory Affairs Specialist

BRIGHT FUTURE PHARMACEUTICAL LABORATORY LTD

Benefits
  • 5-day week
  • Insurance plan
  • Meal allowance
  • Shuttle bus

Responsibilities:
  • Dossier preparation for product registration, especially on Chinese Medicine, Herbal Medicine or Botanical Drugs
  • Preparation of responses to post-submission queries by regulatory authorities
  • Window person for Third Party and Regulatory Authorities in different countries
  • Central management of Registration dossiers (hard copies and electronic files)
  • Coordination with relevant Departments concerned with the preparation of registration dossier
  • Provide updates on the Regulatory Guidelines of the Regulatory Authorities and update trainings to relevant parties
  • Provide weekly and monthly progress report to Supervisor
  • Complete Ad hoc tasks assigned by the Supervisor
Qualifications:
  • Bachelor degree or above in Chinese Medicine or related fields.
  • 1- 2 year working experience in product registration but not a must.
  • Good communication skills;
  • Good command of both spoken and written English, and Chinese;
  • Can work independently under pressure and able to meet tight deadline;
  • Good team player 

We offer competitive package including public holidays, 5-day work week, shuttle bus from Fanling and Long Ping MTR station, medical insurance, free luncheon and discretionary bonus.

Interested parties please send your full resume stating your current and expected salary and date of availability (Data collected will be used for recruitment purpose only) 

More job information
Job ref no. CT3115399-01#0022
Salary
  • N/A
Job Function
Industry
Location
  • Yuen Long
Employment Term
  • Full-time
Experience
  • 1 year - 2 years
Career Level
  • Non-management level
Education
  • Degree
  • Master's degree
Require to Travel
  • No travel