Johnson & Johnson Careers

Beijing-RA Specialist

Beijing, China
Regulatory Affairs

Job Description

Requisition ID: 1805625695W

Responsible for implement registration policies designed by manager and follow up.
  1. Prepare and submit registration application and dossier, follow up testing and evaluation procedure, obtain product license from SFDA independently.
  2. Update registration database, technical document, factory certificate, DOC database when having change.
  3. Work closely to SFDA and testing center, establish and maintain good relationship.
  4. Well coordinate with internal & external customers, have great communication skills – need to liaise with a lot of different parties both inside and outside the company (including Headquarters, Marketing, warehouse, sales Service, testing center and evaluation center etc.).
  5. Adapt to rapid changes in business environment, meet different requirements.

  1. Bachelor or above degree of medical, chemistry, mechanics, engineering, bio or relatives.
  2. Good inter-personal, communication and presentation skill.
  3. Fluency (oral and written) in both Chinese and English.
  4. Be patient and earnest on product registration projects.
  5. Good team player.
  6. Independently handle project ability.

Primary Location
Johnson & Johnson Medical Shanghai Ltd. (7055)
Job Function
Regulatory Affairs
Requisition ID