岗位职责：
• Take ownership in all aspects of project execution.
负责项目运行的各个方面工作
• Coordinate between all disciplines to ensure the overall design is fit for purpose.
在不同专业间进行协调，确保整体设计满足设计初衷
• Assist the project manager for project reporting.
协助项目经理完成项目报告
• Perform work in compliance with PM Group’s Quality Management System.
按照PM Group的质量管理体系开展各项工作
• Perform work in compliance with applicable GB codes and standards.
按照国标开展各项工作
• Ensure PM Group specifications are compatible with GB codes and fit for purpose for the China market.
确保PM Group规范符合国标，满足设计要求，同时满足中国市场需求
• Perform work in compliance with applicable local codes and standards.
按照地方标准开展所有工作
• Participate in the Project Initiation phase including:
参与项目启动，包括：
o Ability to understanding the scope of the project
理解项目范畴
o Defining PM Group’s scope of work
明确PM Group工作范畴
• Work to and input into the project schedule(s), track/report progress and implement controls.
制定项目进程、跟踪报告项目进展、控制项目实施
• Work to and input into project budget, and cost estimates including preparing BOQ and checking vendor costing.
完成项目预算、成本预算，包括准备竞标文件、确认供应商成本
• Execute your designs based on international GMP guidelines and process design for pharma, biopharma and nutritional industries requirements.
完成设计工作，确保其符合国际通用GMP规定流程以及制药、生物制药、营养学领域行业规定
• Execution of validation / qualification procedures for GMP systems.
执行GMP认证过程
• Insure your design is based upon and understanding of GMP requirements for clean utility systems.
理解GMP中关于洁净设施体系要求并据此完成设计工作
• Generate performance specifications and technical specifications for process systems.
制定工艺体系中的运行及技术说明书
• Develop P&ID, equipment layout, piping layout, sections and plans using Auto CAD.
使用Auto CAD完成管路、仪表工艺流程图、设备布局、管道排设及区域分布
• Develop specifications and performance test requirements to facilitate procurement of parts and equipment for Food, Nutrition, Life Science, Pharmaceutical and Chemical Industries.
提出设备要求，以符合食品、营养、生命科学、制药及化工行业的部件及设备采购
• Interview supplier representatives regarding specifications, costs, inspection, and similar problems relating to parts and equipment.
供应商审核，包括零部件及设备的说明书、成本、检验及其他相关问题
• Analyse and reviewing tender proposals for process equipment for GMP compliance and process suitability.
分析审核工艺设备相关标书，确保其符合PM Group标准，适应工艺要求
• Coordinate the design of process systems with architects, mechanical, electrical and instrumentation design engineers.
与建筑师、机械工程师、电气工程师及仪器仪表工程师协调完成工艺系统设计
• Generate and execute Factory / Site Acceptance Test protocols for clean utility and process equipment systems.
就洁净设施及工艺设备体系设计工厂/现场验收测试草案并执行
• Control document revisions and ensure that all issue documents are in compliance with PM Group document management systems.
文档管理，确保所有发布的文档符合PM Group文档管理体系的要求；
• Carry out all duties in accordance with PM Group QMS [Quality Management Systems].
完成所有的工作职责，确保符合PM Group质量管理体系
• Other Ad-hoc duties
其他工作。


岗位要求：
• Working Experience: 5~8 years’ experience on Pharma projects engineering
工作经验：5~8年医药项目设计经验
• LDI or Project management company working experience preferred
设计院或管理公司工作经验优先
• Working place: Based in PM Group SW office, might be relocated to Shanghai office or sites if required
工作地点：成都办公室或者根据需要安排到上海办公室或者项目现场
• English Skill: Good at both writing and speaking is preferred
英语读写熟练者优先

其他信息
语言要求：英语、普通话
行业要求：全部行业