Posted 2 weeks ago
Requirement
- Degree holder in medical Engineering
- 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
Duties:
- 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 Category | Engineering |
