1. 招聘职位
  2. 工作地点
  3. 招聘人数
  4. 发布日期
  5. 应聘

岗位职责

1.下游纯化技术开发和转移放大,GMP生产;

2.参与准备纯化生产相关技术文件起草、修订等;

3.参与纯化工艺开发、表征和验证;

4.按照SOP,确保纯化操作流程和良好记录。

任职要求

1. 制药相关学科大专以上学历;

2. 具有较强的沟通、分析和解决问题的能力;

3. 熟悉使用下游纯化和配液系统设备,有相关工作经验者优先。


岗位职责

1、负责工艺设备设施的巡检、维护保养和维修工作,确保其正常运行;

2、按维修计划、或维修工单要求及GMP要求完成各项维修保养工作,具体实施并及时汇报;

3、参与设备、设施的验收;做好安装、调试等具体操作工作


任职要求

1. Advanced degree in life sciences preferred; 2 years+ of industry experience in regulatory writing;

2. Strong technical background in the field of antibody drug development is a plus;

3. Knowledge of FDA, EMA and NMPA regulations and ICH guidance;

4. Demonstrated writing skills with strong command of bilingual (English and Chinese) language and grammar;

5. Must possess excellent interpersonal, organizational, written and verbal communication skills along with ability to work collaboratively in a team environment;

6. Efficient, organized, and able to handle short timelines in a fast-paced, dynamic environment;

7. Proficient with document management software/systems, such as filing systems and ELN;

8. Prior supervisory experience preferred.

应聘职位
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