长沙招聘

职位描述：
Job Scope:
1、Assist the leader to build quality documents management of research and development
2、Review the integrity, authenticity and standardization of related records;
3、Be in charge of organizing training of related documents
4、Build yearly training plans and organize to implementation for RD staff
5、Be responsible for urging relevant departments to comply with and perform the quality management system and regulations during research and development process
6、Inspect and supervise quality control items of research and development laboratory and track implementation and rectification;
7、Participate in investigation of unexpected events in research and development process.
8、Be responsible for supporting the internal and external audit of the projects.
9、Be responsible for arranging and coordinating the group member`s work.
10、Complete to temporary assignment according to the leaders.

Requirment:
1、Be familiar with the cFDA and FDA relevant regulations.
2、Independently judge, operate, supervise and 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 command of both spoken and written English and Chinese 举报 分享

海南澳美华制药有限公司是香港制药厂有限公司（香港***制药企业）在海南投资成立的全资子公司，同时也是香港澳美在海南的人才培训基地，表现优异的员工将有机会赴港工作。公司在香港总部的技术支持及科学管理下高速发展，目前拥有片剂、胶囊剂、干混悬剂、丸剂等多条gmp生产线，主要致力于心血管及抗生素药物的研发和生产。公司秉承“以精湛科技奉献优质药品，以真诚服务致力人类健康”理念。