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Regulatory Affairs Specialist
Job Description:
1. Familiar with the English operating environment.
2. Responsible for the registration of medical equipment registration, changement, extension and updating.
3. Familiar with medical equipment registration regulations and processes, can be compiled company product inspection registration information to achieve the requirements of TFDA and national health units.
4. To understand the medical equipment regulations and inspection and registration requirements, and the data file management, updated at any time to ensure that companies comply with government regulations
5. Domestic and foreign medical equipment information reading and compilation.

Scientific Limitations: Medical and Health Sciences, Medical Engineering

Language Ability: English Listening: Medium: Medium Reading: Medium Write: Average

Typing speed: 30 words or more

Computer Skills: Word, Excel and PowerPoint, Outlook

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