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Job ID :
58390BR
Location :
China - Shanghai
:
Job Description
  • Responsible for post market product compliance, include but not limited to the medical device products.
  • Be able to collect, monitor analyze and interpret product relevant regulations professionally
  • Be able to collect, monitor, analyze and interpret product relevant industrial standards, national standards.
  • Responsible for preparing the Chinese labeling templates, review and approve Chinese labeling for the import products
  • Host the post market audits
  • Maintain the medical device distribution licenses.
  • Maintain the GSP master data and responsible for the initial approval of suppliers/customers in GSP
  • Other post-market product compliance relevant tasks



Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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