工作职责:
General Description
一般描述
1. Conducting method validation and sample analysis as per plan or protocol.
1. 按照方案进行方法验证及样品分析项目；
2. Comply with GLP regulations in all work and documentation;
2. 在工作中（包括实验记录）严格遵守GLP法规；
3. Perform and review laboratory work, strictly follow SOPs and regulations.
3. 实验室工作严格遵守SOP法规；
4. Write methods and review data packages.
4. 书写分析方法并审核原始数据；
5. Perform instrument maintenance and trouble-shooting as needed
5. 仪器常规维护及故障排除；
6. Complete assigned task on time.
6. 准时完成工作安排。
任职资格:
1. With B.S. above in pharmaceutical or related industry.
1. 医药及相关领域本科以上学历；
2. Good communication with team members.
2. 具有良好的团队沟通能力；
3. Fluent in written and oral English.
3. 熟练的英语读写及口语能力。