邢台招聘

Key areas of responsibility

l Focusing on Automation system life cycle management including upgrade, spare part lifecycle management

l As PLC/HMI/SCADA/DB backup responsible for platform access and security solutions

l Maintenance Automation system of CE or IT system in compliance status

l Prepare new solution for production and verify the feasibility

Main Job Tasks 主要工作任务:

Support for production automation systems

· Preparation and execution Automation system PM /CM plan for fast action in emergency maintenance activities and right execution in PM activities timely, be proficient in SAP PM and *** for routine maintenance &spare part management

正确制定预防性维修计划，准确及时执行预防性维护以及应急维修，熟练使用SAP系统进行维修以及备件管理

· Daily operation/process confirmation of automation system (pharmaceutical utility, Aseptic relevant systems like: Formulation/Filling Line/SIP/CIP/UW/CPE/Inspection ), guarantee all systems are in safety/stable/high-efficiency running status;

日常运行相关自动化系统（制药工程，无菌生产工艺相关，如无菌配方/无菌罐装/清洗和灭菌/检查等相关系统），并对系统进行日常过程确认，确保所有系统在安全/稳定/高效运行状态

· Actively initiate continued improved automation system to meet the requirement of system stable, safe and high efficiency running; Cause analysis and PM/CM action setting up by Lean thinking and tools

主动实施相关自动化系统的持续改进，精益生产的工具和理念应用到预防性维护，日常维修以及故障根本原因分析

· Development and Implementation of system reliability/energy saving improvement projects and have the competence in CR/DV handling during daily operation & maintenance

发展和实施有关系统稳定运行和节能运行项目，并且具备处理项目改进以及日常运行维护中的CR/DV能力

· Technical support of different engineering disciplines in project upgrade and have right competence in external vendors, minor projects management, validation process competence and GMP audit/inspection readiness

系统项目改进过程中技术工程支持并且对外部供应商以及内部改进项目实施管理，同时具备系统验证能力和GMP内审和外审能力

Automation documentation following up to meet GMP requirement and fluent writing and updating automation system SOPs. Make sure the system running in compliance status

· Professional Experience专业经验:

· 3 – 5 years manufacturing experience in pharmaceutical automation systems of cGMP regulated pharmaceutical industry or in life science industry preferable

拥有3-5年制药行业相关经验并熟悉相关GMP规范

· 3+ years engineering experience in automation Designing, Maintenance, operation, Process Improvement, Root Cause Analysis (RCA)

具备6年以上自动化相关的设计，运行，维修，工艺改进以及故障根本原因分析等技术工程类经验

· 具备自动化，计算机信息技术，制药工程，电气系统以及制药行业或其他GMP行业相关自动化工程知识背景

Proven expertise in execution of operation& maintenance activities, following up on results, and revising the work plan for complex problems being resolved by cross functional teams on time

· 具备实际运行和维护专门知识技能，并且具有应急复杂问题分析处理能力以及跨部门协作沟通解决问题能力

· MUST Proficient in PLC/SCADA/DCS and other basic automation relevant technology, master in at least one programming skill by using Python/C#/JAVA or other mainstream programming language, 2-3 projects about Big-data/Artificial

必须精通PLC/SCADA/DCS等自动化领域的通用技术，掌握至少一种主流编程语言（如Python/Java/C#VB）。

Education Background: 教育背景

· A bachelor/master’s degree in Automation /Mechanical/ Computer Science and technology/ Information Technology/Electrical Engineering/AI or other relevant engineering majors

自动化/机械/计算机/信息科学/电气工程/人工智能等相关工程类专业大学本科及以上教育背景

· Excellent command of written and spoken English

良好的英语书写和沟通能力

诺和诺德在中国
诺和诺德是中国市场的领导者，一直以改变为己任。诺和诺德（中国）制药有限公司于1994年成立，二十几年来业务一直保持强劲增长。公司总部设在北京，产品和服务遍及全国所有省、直辖市及中国港澳台地区。截至2017年底，诺和诺德在华员工总数4329人。诺和诺德是在中国建立研发中心的生物制药公司。位于北京的研发中心是诺和诺德全球研发体系的组成部分，致力于与总部合作研发新产品及新生产工艺。诺和诺德在中国的生产厂位于天津，是公司的国际化战略生产基地。公司对工厂提供了大量的资金投入和技术支持，向全球以及中国市场供应产品。诺和诺德在中国的不断发展反映了公司对中国市场的承诺。

Novo Nordisk in China
As the leader in the Chinese market, Novo Nordisk has always been committed to Changing.
Founded in 1994 and headquartered in Beijing, Novo Nordisk’s presence in China has been growing for more than 20 years.Headquartered in Beijing, providing products and services across mainland China as well as Hong Kong, Macau and Taiwan of China. As of the end of 2017, Novo Nordisk employed over 4,329 employees in China.