Assistant Product Regulatory Affairs Coordinator – ISO13485 / CFDA

Posted 7 months ago

Job Descriptions:

  • Works closely with line managers, maintaining the COPs in comply with ISO 13485 and 9001.
  • Travel to China is required.

 Job Requirements: 

  • Degree in Bio-medical Engineering, Legal Studies or related disciplines
  • At least 1 year related experience, preferably in medical devices industry
  • Good knowledge in ISO 13485, ISO9001, 510K, CE, CMDCAS, CFDA legislation
  • A team player and detail minded
  • Good command of English and Mandarin

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Job Features

Job CategoryOthers, Technician

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