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MITG_Regulatory Affairs Supervisor

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Regulatory Affairs
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16000JH8 求人番号
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Qualifications and requirements

  • Experiences and strong tool kits in medical device regulatory
  • Team management experiences
  • Connection with CFDA and other related government administration
  • Good communication skills
  • Good learner and flexibility to change
  • Currently working in the registration of medical device field.
  • Working experience on capsule and/or RF products would be a plus.

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