作为最终用户参与和支持青岛工厂的项目建设
Support project team to deliver Qingdao pMDI project as end user
参与到项目的不同阶段,作为最终用户提供有价值和专业的建议到项目建设中Fully involved in different project phase and have valuable input as end user
学习并运用其他工厂和行业的最佳实践到新工厂Learn and apply best practice from other sites and other experiences to Qingdao project
端到端的思维持续标准化和持续改善的理念和能力,通过项目期间的参与,实践为未来的商业化生产的垂直启动和成功做好充足的准备End to end mindset to be involved in project and ensure standardization and continuous improvement to BAU vertical startup through expertise, lean and experience gained from project phase
良好的问题解决能力和持续改进的能力,确保项目C&Q,PQ/PV的成功Strong PPS and CI capability to ensure C&Q, PQ/PV successfully
生产设备维护
Production equipment maintenance
负责对配料&制剂&罐装设备维护及软件管理,定期进行预防性维护, 准确及时填写设备维护,维修记录Responsible for dispending &formulation & filling equipment maintain and software management, carry out routine preventive maintenance plan together with engineering group, fill and keep preventive maintenance and repairing records correspondingly and timely
及时解决生产中出现的设备故障Identify equipment fault and perform prompt and efficient repairing
根据现场经验提交维护体系更新建议Submit update suggestion to maintenance system based on shop floor experience
如需要,起草相关工作指导或标准操作规程Draft technique WI/SOP as required
及时定购设备备品备件,以满足生产的需求。Engineering spare parts ordering and stock management to support production needs
对配料&制剂&灌装设备及软件的缺陷进行改造以使其更好的发挥性能Modify any defectives of dispensing & formulation & filling equipment and software to get better performance with creative and effective solution
起草设备升级改造的验证文件Draft verification document for equipment update/modification
生产流程优化建议Suggestion for optimizing operation procedure
设备操作Equipment operation and validation support
需要时,在批生产过程中负责相关设备操作,(如隔离器、制剂系统、灌装机)Operate certain equipment in proper way when production batch happens when required.(such as isolator、formulation system、filling machine)
在维护或维修过程中,能以超级用户运用设备服务功能。Be able to operate related machines within service function as super user while maintaining and repairing
给验证或再验证提供支持Support Validation & Revalidation activity.
GMP/合规/SHE相关责任Responsibility for
GMP/Compliance/SHE
在进行一切与业务相关活动时都严格遵守公司 GMP、SHE、合规及其与职位和职责相关的支持性政策与标准Conduct all business activities in compliance with the GMP /SHE/Compliance supporting Policies and Standards related to position and responsibilities
日常工作中与带班/生产负责人/流程团队成员紧密协调Well coordinate with group leader/PF/PCO members in daily operation
必需的Essential
工程领域的本科或以上学历
Bachelor or above degree, major degree in engineering field
机械,电气电子,工业自动化知识
Mechanical & Electrical & Electronic knowledge, Industrial automation
熟悉自动控制系统中各种传感器的基本工作原理
Be familiar with the basic working principle of various sensors in automatic control system
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,乐于分享和发展团队成员的技能High teamwork spirit and be willing to share and develop team member skills
Date Posted
18-3月-2025Closing Date
30-7月-2025AstraZeneca 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.