MITG_Regulatory Affairs Supervisor
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- 16000JH8 Numéro de demande de personnel
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- Sep 30, 2016 Date de publication
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.