Job description

Requirements

  • Entry level
  • No Education
  • Salary to negotiate
  • Beijing

Description

product registration related including new and renewal
handing registration process for S1/2 including document requirement dossier prepare, submit to CFDA, Follow up evaluation procedure, sample ordering type testing, solve various problems in whole process, file dossiers with consistent requirement;
Ensure to obtain the regulatory permits on time, in support of the organization's business plan especially product launch plan;
Establish working relationship with officials and experts in authorities, good communication and negotiation with officials and experts to guarantee smooth registration;
Pay attention to the market information such as the competitors with the analysis;
To coordinate the post surveillance project. 

Qualifications
Medical or related education background and knowledge;
3-5 years medical device experience in regulatory affairs
good communication skills;
Good time management skills;
Well computer operating;
Better English and Chinese in Writing and oral

Primary Location
China-Beijing-Beijing-
Organization
Johnson & Johnson Medical Shanghai Ltd. (7055)
Job Function
Regulatory Affairs
Requisition ID
1905724239W

About the company

If you’re thinking about taking your career to a place where you can be seen for the talent you bring to your work, where you’ll have a chance to be the driver of your own career, and where others share your passion for caring and success, then we invite you to explore Johnson & Johnson. BE VITAL in your career and make a unique mark. Join the approximately 129,000 men and women who work within our companies and touch the lives of more than a billion people around the world every day.

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