Position Responsibility:
1. Responsible for clinical test or appraisal of product regarding to IVD product and clinical product due to registration change
2. Responsible for clinical authenticity inspection tasks
3. Collect, classify, and archive all regulations, documentations, and guidance published by national Food and Drug Administration Bureau, and grasp the trend of IVD rules and regulations by all means.
4. Responsible for sample requirement management
5. Responsible for other tasks assigned by superiors
Position Requirement:
1. Education requirement: graduate degree or above, bio-pharmaceutical relevant major or working experience is preferred
2. Proficient office software skills, strong language organization ability, and good at communication and cooperation
3. Proactive and patient during the work, and strong sense of responsibility, team work spirit and sense of group honor
4. Able to go for short term business trip
