Product Regulator Supervisor / Assistant Product Regulatory Manager – Medical Device

Posted 2 months ago


  • Degree holder in medical Engineering
  • 3-5 year in Regulatory in medical device in Trading or Factory
  • Good knowledge in ISO 13485, ISO9001, 510K, CE, CMDCAS, CFDA legislation.
  • Proficient of English and Mandarin


  • Handle regulatory affairs, such as product license registration/renewal, coordinating customers/internal audits, preparing of ISO documentations and etc.
  • Comply with ISO 13485.
  • Conduct training for staff to fulfill the regulatory requirements. 
  • Good knowledge in ISO 13485, ISO9001, 510K, CE, CMDCAS/MDSAP, CFDA / NMPA legislation.

We are welcome applicants resend resumes to us even you have applied jobs in our company before.
(Personal data submitted are for recruitment purpose only.)

Job Features

Job CategoryOthers, Technician

Apply Online

A valid email address is required.
A valid phone number is required.

I have read and accepted the Collection Statement and Privacy Policy and agree to the use of my personal information for the purpose for recruitment purpose only.