支持生产体系的搭建以支持未来的商业化生产
Support to setup manufacture system to ensure following BAU smoothly
生产和日常操作
Production and routine operator
遵守GMP和SOP的相关规定
Follow GMP & SOP
遵守公司政策
Follow AstraZeneca policy
能够独立操作各生产工段（配料、制剂、罐装、组装线、包装线）和IPC设备，明确岗位职责并考取岗位上岗证
Able to each production section (dispensing, formulation, filling, assembly lines, packaging lines)operate Assembly line machine、 Packing line machine and IPC machine ,and know the job responsibility and get the job certificate
熟知岗位中间控制职责，如果经过中间控制知识及操作技能的培训并考核合格后，承担生产过程中的中间控制职责
Familiar with in-process-control, take the IPC responsibility if finish IPC training and pass the test
及时向流程负责人/一线生产经理反馈当班过程中的人员行为和绩效，必要时对员工进行辅导
Report to process facilitator/FLM about people behavior and performance when on duty, coach employees if needed
自主解决当班过程中产线的各种问题解决，必要时升级
Facilitate problem solving when on duty and escalate if needed
参与偏差和投诉等质量事件调查
Participate in the deviation & complaint investigation
进行生产线的清洁、清场
Packing line Cleaning
积极主导现场问题的解决，并协调生产资源
Actively lead problem solving in line and coordinate line resource
具备相应的精益技能和意识，并提出改善建议，组织产线持续改进项目实施
Propose continuous improvement ideas based on lean skills and mindset, lead improve project execution
保持现场良好的5S状态
Keep good 5S status in shopfloor
TPM
确保员工按照点检表要求进行点检，并不断优化点检内容
Ensure employees follow the spot check form and continuously improve the form
及时报告设备的异常，并能独立解决复杂设备问题
Report equipment abnormal in time and solve complex equipment problems
参与设备的日常保养并主导AM活动
Participate in general upkeep and lead AM activities
协助维修人员进行设备的维修和保养
Help equipment maintenance and upkeep with engineer
培训
Training
接受相关GMP和SHE的培训
Accept relative training of GMP&SHE
培训新员工和其他人员岗位操作技能
Train new staff and others’ skills
掌握多技能，并推进产线员工多技能发展
Have multi-skills and promote employees’ multi-skill development
组织培训资料的编写和操作标准的制定，并检查标准是否执行到位
Organize drafting training materials and process standard, regularly do standard confirmation
能够独立编写GMP相关文件，如SOP WI等
Can draft GMP related documents such as SOP WI
GMP 要求
GMP requirements
理解业务活动中涉及GMP的相关内容及可能对产品质量产生的影响
Understand the impacts of daily work on GMP requirements and product quality
参加GMP相关培训，确保业务活动持续符合GMP要求
Attend GMP trainings and ensure that daily work is compliant to GMP consistently
严格执行本岗位的GMP相关规程
Strictly follow GMP SOPs.
向直线经理或QA沟通工作中遇到的GMP相关问题
Report to line manager or QA about GMP questions encountered in daily work
其它Other tasks
根据工作需要完成文件工作
Paper work or report upon request
提供跨部门支持
Functional support
文件工作
Documentation
Requirements
药学或理工科相关专业本科学历及以上Bachelor degree or above with pharmaceutical or Engineering related background
具备基本的英语读写能力Basic English in reading & writing
能应用微软常用办公软件Basic Microsoft office skill
个人特性Personal character
➢与团队成员真诚交流
Be honesty to communicate with each other in team
➢在高强度工作压力下具有很强的责任感
Be responsibility under high work pressure
➢团队工作精神，乐于分享
High team work spirit and be willing to share
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
