Responsibilities: Design and carry out   maintenance level 1 and 2 and daily check lists Implement lubrication sheets Quick response to the production line problems ,list, investigate and solve equipment outstanding issue Do some little modification on machine to develop machine reliability and efficiency Focus on TPM to improve operators skills , solve the machine hidden issues , control the overall downtime and so on By learning to think constantly, offer innovation for the RPC problem of the ...

Short role description Leads formulation and process development activities for new molecular entity. Ensure suitability of all development work to meet the regulatory requirements of Global and China CMC submission. Typical Accountabilities Leads formulation and process development activities for new molecular entity. Author Drug Product sections for CMC dossier submissions, suitable for Global and China submission. Lead technical transfer between AstraZeneca sites for Clinical or Commercial Ma...

Responsibilities: Ensure team members understand and implement   relevant policies, procedures, laws, regulations Participate in training provided and know where to find the knowledge we require Understand budget responsibilities Understand and adhere to financial tools and processes Appropriate mechanisms are in place to track and control manpower and non-manpower expense within area, within budget Develop subordinates’ capabilities and knowledge by on job coaching Holiday , absence management ...

IT QUALITY MANAGER Do you have expertise in, and passion for, IT Quality Management? Would you like to apply your expertise to impact the End User Services in a company that follows the science and turns ideas into life changing medicines? If so, AstraZeneca might be the one for you! ABOUT ASTRAZENECA AstraZeneca is a global, innovation-driven BioPharmaceutical business that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious...

Landing Functions could be: Technical, Quality, Supply Chain, Production, Lean& Digital, Engineering Location : Wuxi, Jiangsu Province Description of program: This challenging, stretching and inspiring China Operations Management Trainee Program provides the opportunity to customize experience within the business. The program focuses on giving them in-depth experience across multiple areas of our business. It will be split into several different placements, and each role will give you valuab...

•      Finish the routine analytical work accurately and timely 准确及时地完成日常分析工作    •      Conduct the maintenance and validation for instrument periodically based on plan and keep it in good status. 按计划定期做好仪器的维护和验证工作并使其处于良好状态。 •      Double-checking the BAR. 复核批化验记录 •      Responsible for the management of  chemical reagents/ reference standard/ consumables, including purchase and maintenance of safety inventory 负责化学试剂/对照品/易耗品的管理包括采购及维护安全库存 •      Responsible for the handling and disposal of lab w...

•      Finish the routine analytical work accurately and timely 准确及时地完成日常分析工作    •      Conduct the maintenance and validation for instrument periodically based on plan and keep it in good status. 按计划定期做好仪器的维护和验证工作并使其处于良好状态。 •      Double-checking the BAR. 复核批化验记录 •      Responsible for the management of  chemical reagents/ reference standard/ consumables, including purchase and maintenance of safety inventory 负责化学试剂/对照品/易耗品的管理包括采购及维护安全库存 •      Responsible for the handling and disposal of lab w...

•      Finish the routine analytical work accurately and timely 准确及时地完成日常分析工作    •      Conduct the maintenance and validation for instrument periodically based on plan and keep it in good status. 按计划定期做好仪器的维护和验证工作并使其处于良好状态。 •      Double-checking the BAR. 复核批化验记录 •      Responsible for the management of  chemical reagents/ reference standard/ consumables, including purchase and maintenance of safety inventory 负责化学试剂/对照品/易耗品的管理包括采购及维护安全库存 •      Responsible for the handling and disposal of lab w...

Responsibilities: - Onsite inspection, identify potential risk, help enhance the quality sense of the operator - Handling, investigation and assessing of quality issues - Establish, execute and track CAPA - Review batch production report - To be involved in regulatory inspections and self-inspection - Ensure to fulfil the KPIs of QA - Support PET business processes regarding compliance and quality - Identify the quality risk during daily work, improve continuously - Communicate with other AZ sit...

Responsibilities: Systech system & GST Accture E-coding system Traceability process data flow between systems Kepware/OPC of PI interface Application work performance and data quality of traceability Lvl 2 system monitoring Interface between equipment & PI platform monitoring， such as NAS or other connecting device Incident and problem reporting Traceability data issue in Systech/GST/ Accture E-coding system/PDM In a Pi source system with PI platform Computerized system management...

Operations Global Graduate Associates Programme Location: Wuxi Salary: Competitive If you have a bachelor’s or master’s degree and a desire to explore your potential within a global biopharmaceutical organisation, our Operations Global Graduate Associates Programme could be the perfect start to your career. You’ll gain invaluable insight, exposure and opportunities across our diverse, international organisation. We’ll accelerate your learning and development and help prepare you for a future lea...

工作职责： -遵守GMP, 按照SOP要求进行操作 -根据看板生产指令进行生产 -及时完成BPR及使用日志，并汇报偏差 -生产线清场 -运行状态，及时汇报异常状况 -协助机修人员完成设备维修及维护保养 -按照要求对物料及厂房进行清洁消毒 任职要求： -1年以上外资企业生产工作经验 -良好的沟通能力 -高度的责任心 -有高洁净生产区域的工作经验优先 Date Posted 18-8月-2021 Closing Date 30-8月-2021 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...

工作职责： -遵守GMP, 按照SOP要求进行操作 -根据看板生产指令进行生产 -及时完成BPR及使用日志，并汇报偏差 -生产线清场 -运行状态，及时汇报异常状况 -协助机修人员完成设备维修及维护保养 -按照要求对物料及厂房进行清洁消毒 任职要求： -1年以上外资企业生产工作经验 -良好的沟通能力 -高度的责任心 -有高洁净生产区域的工作经验优先 Date Posted 13-8月-2021 Closing Date 11-11月-2021 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 w...

•      Finish the routine analytical work accurately and timely 准确及时地完成日常分析工作    •      Conduct the maintenance and validation for instrument periodically based on plan and keep it in good status. 按计划定期做好仪器的维护和验证工作并使其处于良好状态。 •      Double-checking the BAR. 复核批化验记录 •      Responsible for the management of  chemical reagents/ reference standard/ consumables, including purchase and maintenance of safety inventory 负责化学试剂/对照品/易耗品的管理包括采购及维护安全库存 •      Responsible for the handling and disposal of lab w...

Job Responsibilities: 中央监控系统中央站维护 开利网络，PLC及其他自控系统维护 用户需求分析 提供解决方案 项目实施及管理 信息咨询 与供应商沟通协调等 起草设施URS. 变更起草及跟进。 GMP内审偏差跟进 在进行一切与业务相关活动时都严格遵守公司GMP、行为准则、SHE、合规及其与职位和职责相关的支持性政策与标准 识别和了解本部门的安全危险因素 制定和执行SHE方案以强调在相应区域的关键SHE事件并确保跟进措施的落实执行 SHE 遵守SHE承诺书上的要求 Requirements: 至少电气及自动化本科毕业 至少5年公用工程维修或者工程项目改造经验 熟练的英文读写及沟通能力 跨国企业公用工程自动化控制方面工作经验 计算机系统验证的项目经验 GMP生产工厂工作经验 Date Posted 12-8月-2021 Closing Date 10-11月-2021 AstraZeneca embraces diversity and equality of opportunity.  We are committed to building an in...

•      Finish the routine analytical work accurately and timely 准确及时地完成日常分析工作    •      Conduct the maintenance and validation for instrument periodically based on plan and keep it in good status. 按计划定期做好仪器的维护和验证工作并使其处于良好状态。 •      Double-checking the BAR. 复核批化验记录 •      Responsible for the management of  chemical reagents/ reference standard/ consumables, including purchase and maintenance of safety inventory 负责化学试剂/对照品/易耗品的管理包括采购及维护安全库存 •      Responsible for the handling and disposal of lab w...

Responsibilities Pharmaceutical Quality systems management 质量体系管理 ? Coordinate Quality key systems in place and improvement, including, but not limited, 组织和协调关键质量体系的运行和改善，包括，但不限于， ? GMP training GMP培训 ? Document management文件管理 ? QAA management质量保证协议的管理 ? CAPA address, feedback and follow up CAPA的制定，反馈和跟踪 ? Change control生产变更 ? Quality risk management风险管理 ? Self-inspection自检 - KPI data collection and reporting to global KPI数据收集和报告给总部。 - Quality performance review and r...

Responsibilities: Onsite inspection, identify potential risk, help enhance the quality sense of the operator Handling, investigation and assessing of quality issues Establish, execute and track CAPA Review batch production report To be involved in regulatory inspections and self-inspection Ensure to fulfil the KPIs of QA Support PET business processes regarding compliance and quality Identify the quality risk during daily work, improve continuously. Communicate with other AZ sites regarding to q...

Responsibilities: Facilitate the deployment of site digital transformation roadmap and clarify the direction for site improvements (the next 1 ~ 2 years) Define operational improvement targets, establish site performance improvement plan which are enabled by digital technologies Support PETs and Functions to establish digital transformation plan and introduce digital use cases to enable performance improvement Manage site digital project portfolios  Facilitate Site/PETs for business analysis to ...

Responsibilities: Facilitate the deployment of site digital transformation roadmap and clarify the direction for site improvements (the next 1 ~ 2 years) Define operational improvement targets, establish site performance improvement plan which are enabled by digital technologies Support PETs and Functions to establish digital transformation plan and introduce digital use cases to enable performance improvement Manage site digital project portfolios  Facilitate Site/PETs for business analysis to ...