- 招聘人数：1 人
- 到岗时间：不限
- 年龄要求：35周岁以上
- 婚况要求：已婚
Job Scope:
1、Assist the leader to build quality documents management of research development
2、Review the integrity, authenticity stardization of related records
3、Be in ge of organizing training of related documents
4、Build yearly training plans organize to implementation for RD staff
5、Be responsible for urging relevant departments to comply with perform the quality management system
regulations during research development process
6、Inspect supervise quality control items of research development laboratory track implementation rectification
7、Participate in investigation of unexpected events in research development process.
8、Be responsible for supporting the internal external audit of the projects.
9、Be responsible for arranging coordinating the group member`s work.
10、Complete to temporary assignment according to the leaders.
职位要求：
Requirment:
1、Be familiar with the cFDA FDA relevant regulations.
2、Independently judge, operate, supervise deal with the quality problems during the development phase.
3、Be good at communication ability, coordinate all departments to assure the information to be delivered.
4. Good comm of both spoken written English Chinese
