Johnson & Johnson Careers

Senior RA Specialist_Joint

Beijing, China
Regulatory Affairs

Job Description

Requisition ID: 1905774355W

- Product registration related including new and renewal
o Handling registration process for endomechanical products, including
 Document requirement
 Dossier prepare
 Submit to NMPA
 Follow up evaluation procedure
 Sample ordering, type testing
 Solve various problems in whole process
 TRD review and submission preparation
o Ensure to obtain the regulatory permits on time, in support of the organization’s business requirements
o Having a good and consistent communication with local marketing and known well the business plan especially product launch plan
o Figuring out a rational working registration plan
o Keeping all medical device relevant regulations in mind and having the own opinion on revision when necessary
o To coordinate the post market surveillance and Recall with the written explanation if happening
o Working for product related copy review with the regulatory opinion
o Supporting Chinese IFU and labeling for product related
o Compliance company policy, HCC and QA
o Participate the related standard and regulation conference/revision

- Being proactive to participate the industrial activities to contribute the constructive suggestion

- Paying attention to the market information such as the competitors’ with the analysis

 Being involving into team working such as department meeting logistic arrangement

- Maintain & Input database like: RA database, RTL…

- Provide monthly report & analysis including latest registration status & post market surveillance.

Good communication skill
Better English and Chinese in writing and oral
Well computer operating
Good time management
Medical, laboratory or related education background and knowledge
4 Years Medical Device registration experience

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