By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use I further attest that all information I submit in my employment application is true to the best of my knowledge.
1、负责区域内现场管理，持续提高现场8S、质量、生产力。
2、分析和排除设备及设施简单故障，在规定范围内调整设备、设施参数以达到最优生产结果。
3、根据SOP、GMP及EHS相关要求完成日常生产操作，达成项目、产量、质量目标。
4、负责区域内员工培训及考核及员工技能提高，包括试用期员工管理。
5、负责区域内员工目标设定、绩效评估及面谈。
6、根据生产计划，安排人员排班，合理分配资源，完成生产线任务。
7、跟踪实施制剂区域内的改善活动，并进行评估。
8、及时处理现场发生的异常情况并调查原因，负责CAPA的实施。
9、负责制剂SOP、FORM更新；起草变更、偏差等文件；负责批记录及其它记录的审核。
10、确保良好地激励生产团队及其他职能良好的合作关系。
11、完成上级领导交办的其他任务。
Tianjin, China
Employee
Regular
Full time
We strive to transform lives. While the science we advance is constantly evolving, our core purpose is enduring. For more than two centuries, our values have guided us to do what’s right for patients and for society.
We know that changing lives requires us to do things differently. We start by listening to and addressing what really matters to patients, the people who love them, and those in the healthcare system who provide care. And that’s what inspires us all to be bold, push boundaries and set new standards that open up greater opportunities.
Read our community guidelines: https://takeda.info/communityguidelines
