Johnson & Johnson Careers

Technical Support - RAS, Trauma/Spine/CMF

Beijing, Beijing
Regulatory Affairs

Job Description

Requisition ID: 1805652315W

1.     Principal Duties and Responsibilities (General Summary essential functions and authorities, etc.)


l  Adherence to J&J credo and industry code of conduct, ethics and good regulatory practices, align team members with J&J credo, ensure 100% compliance with local legislation, global regulatory policies, J&J credo

l  Provide technical and regulatory support for TCMF&SPINE products, give suggestion or advice to TCMF&SPINE line, ensure the on-time Launches for TCMF&SPINE products within pre-defined percentage.

l  Maintain effective communication with stakeholders and TCMF&SPINE RA team. Work closely with marketing team in providing effective operational support for entire product registration lifecycle.

l  Take line management responsibility and provide leadership, motivate the group to work more efficiency, manage and develop people and talent, to build a collaborative, high performing team.

l  Strengthening collaboration with CFDA, provincial FDA and other external stakeholders such as testing lab, industry committee. Work with mentioned parties to maximize the compliance with external Technical Standards and Regulations.

l  Provide regulatory assessment/expertise at the early stage of Strategy for TCMF&SPINE products line.

l  Crisis management.


l  Business sense, strategic thinking

l  Good communication skill

l  Good project management skills, good leadership skill

l  English fluent in reading, writing, oral and listening.

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