Sanofi
Process,PlantandC&QEngineer
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Process, Plant and C&Q Engineer at Sanofi. Skills: Process, Plant, C&Q (Commissioning and Qualification), Validation (IQ/OQ/PQ), CAPA, GMP, HSE, SOP. Lead the site Process, Plant & CQ team. Ensure sufficient resources for process, plant & CQ activities”
What You'll Achieve.
Ensure sufficient resources available for all process, plant & CQ activities; Ensure CQ standards are in compliance with regulatory requirements; Enhance efficiency, safety, and quality; Support the development of energy-saving projects; Participate in and implement energy-saving projects; Participate in and implement ISO50001 qualify
Industry & Context.
Solve the problem occurred during the work independently; Investigation of unplanned disruptions, breakdowns and deviations; Develop CAPAs
Special operations require special training and qualification
What They're Looking For.
Must Have
Bachelor’s Degree in engineering or equivalent degree, Familiar with Assembling & packaging equipment and processes, Knowledge of GMP regulatory requirements for CQ activities, Ability to defend and justify CQ plans and practices during internal/external audits, Good English writing and communication skills, Technical writing and investigation techniques
Nice to Have
Previously worked at MNC company
What You'll Do.
Lead the site Process
Ensure sufficient resources for process
plant & CQ activities
Develop and execute equipment validation protocols (IQ/OQ)
Lead investigations and develop CAPAs for unplanned disruptions
breakdowns and deviations
Identify improvement opportunities for critical systems
Act as an SME for quality related discussions during audits/inspections
Provide support to Capital Projects
Implement process improvements to enhance efficiency
Participate in applicable commissioning operation procedures
Ensure CQ standards are in compliance with regulatory requirements
Provide input on resource allocation
and timelines for process
plant and CQ activities
Manage AL9 group packaging line commissioning and qualification (URS
Advise on system lifecycle changes (upgrades
Ensure HSE responsibilities are met
Support and implement energy-saving projects
Participate in and implement ISO50001 certification
Report product complaints and adverse drug reactions
Participate in and complete personal training
Operate in accordance with SOP standards
Fill in GMP documents and records
Report abnormal conditions
Perform activities related with Medical Device according to GSP regulations
How You'll Work.
Team & Collaboration
Work with cross-functional teams; Provide support to Capital Projects; Participate in daily + QDCI meetings; Cooperate with accident investigation
Communication Scope
Good English writing and communication skills; Technical writing; Investigation techniques; Cross-functional team communication; Reporting abnormal conditions; Reporting HSE problems; Providing information during accident investigation
Process & Methodology
Resource allocation, Budget management, Timeline management, Capital Projects support
Full Job Description
**Job title****职位名称** : Process, Plant and C&Q Engineer 工艺工程师 * Location工作地点: 北京 **About the job工作职责** **Our Team****我们的团队 :** Manufacturing & Supply consists of 3 manufacturing platforms based on global business units, as well as supporting functions of Quality, Market Supply and Strategy. We are committed to making best class medicines with excellent strategies and tools and delivering them to our patients. _制造与供应事业部包含以_ _3_ _个全球事业部为基础的制造平台 ,以及质量、供应商、精益战略等支持部门。致力于用优异的战略和工具制造优质的药品并传递到患者手中。_ _Take the lead: Aim higher, act for patients, be bold, lead together_ _敢为人先 :志存高远,心系患者,敢于创新,聚力同行_ **Main responsibilities****职责描述 :** * _Lead the_ _site_ _Process_ _,__plant & CQ team_ _(_ _internal or external_ _)_ _and ensure sufficient resources available for all process, plant & CQ activities __in accordance with site Q &V procedure._ _主导工厂工艺_ _,__调试与确认团队 (内部或外部),并根据现场需求和战略性人力资源规划,确保所有工艺、装置和调试与确认活动均有充足的资源并且符合工厂_ _Q &V_ _流程要求。_ * _Develop and execute equipment validation protocols (IQ/OQ)__, l_ _eads investigations & develops CAPAs for unplanned disruptions, breakdowns and deviations_ _of Process related_ * _编制并执行设备验证方案_ _(IQ/OQ),__主导调查并制定针对工艺相关意外中断、故障和偏差的纠正和预防措施_ _(CAPA)_ * _Identify improvement opportunities for critical systems in the project phase_ _在项目阶段识别关键系统的改进机会_ * _Act as an SME for a quality related discussions during audits/inspections and provide support to Capital Projects as required_ _在审计_ _/__检查期间 ,作为质量相关讨论的专家,并根据需要为资本项目提供支持。_ * _Implementing process improvements to enhance efficiency, safety, and quality during the project phase and also routine management_ _在项目阶段和日常管理中实施流程改进 ,以提高效率、安全性和质量_ * _Participate in applicable_ _commissioning operation procedures_ _参与与实施调试确认规程的应用_ * _Ensure CQ standards are in compliance with regulatory requirements_ _确保_ _CQ_ _标准符合法规要求_ * _Provide input on resource allocation, budget for process, plant and CQ activities, and timelines for CQ activities_ * _为工艺、工厂和调试与确认活动的资源分配、预算以及试与确认活动的计划提供意见_ * _全流程管理_ _AL9_ _组包装线调试确认工作 ,包括_ _URS,
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