Job title职位名称: Automation Engineer
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。
Main responsibilities职责描述:
Responsible for equipment selection, procurement technical support, installation, commissioning, and validation of AL9 A&P line equipment
负责AL9组包装线设备的选型、采购技术支持、安装调试和验证等工作
Participate in equipment-related technical documentation, including URS, DQ, IQ, OQ, and other documents
参与设备相关技术文件,包括URS、DQ、IQ、OQ等文档
Resolve technical issues(Automation, Electrical, Mechanical) during project execution to ensure equipment functionality and performance meet production requirements
解决项目执行过程中的技术(自动化,电气,机械)问题,确保设备功能和性能满足生产需求
Coordinate with equipment suppliers, engineering teams, and production departments to ensure project progress according to plan
协调设备供应商、工程团队和生产部门,确保项目按计划推进
Supervise equipment installation and commissioning processes to ensure compliance with design requirements and industry standards
监督设备安装和调试过程,确保符合设计要求和行业标准
Participate in risk assessments and develop corresponding control measures
参与风险评估并制定相应的控制措施
Participate in packaging line layout and process flow design
参与包装线布局和工艺流程设计
Assist in developing project implementation plans and budgets
协助制定项目实施计划和预算
Review equipment design proposals and drawings
审核设备设计方案和图纸
Supervise equipment manufacturing process and organize Factory Acceptance Tests (FAT)
监督设备制造过程,组织工厂验收测试(FAT)
Organize Site Acceptance Tests (SAT) and resolve technical issues
组织现场安装调试(SAT),解决技术问题
Handle technical deviations during the acceptance process
处理验收过程中的技术偏差
Improve equipment technical documentation and operating procedures
完善设备技术文档和操作规程
Organize equipment operation and maintenance training
组织设备操作和维护培训
Design and implement automation solutions for AL9 (SCADA, DCS, PLCs)
为AL9设计和实施自动化解决方案(SCADA、DCS、PLC)
Ensure compliance with industry standards and regulations.
确保符合行业标准和法规要求
Optimize production processes through automation.
通过自动化优化生产流程
Follow cybersecurity protocols to protect systems.
遵循网络安全协议以保护系统
· HSE Responsibility
安全职责:
- everyone is responsible for HSE, each staff and workers should be in their respective posts, conscientiously perform their duties, do a good job of their own work, the safe production of their post is directly responsible.
HSE人人有责, 每个职工都应在各自的岗位上, 认真履行职责, 做好本职工作, 对本岗位的安全生产负直接责任。
- Careful care and correct use of machinery, equipment, tools and labor protection supplies, finished products, semi-finished products, materials and waste should be stacked in a designated area, to maintain a clean working environment, shall not affect the operation and passage of personnel.
精心爱护和正确使用机器、设备、工具及劳动保护用品, 成品、半成品、物料及废物等须堆放在指定区域, 保持作业环境整洁, 不得影响人员操作和通行。
- Check the safety of machines, equipment, tools, electricity and working environment before and during class to prevent dangerous situations such as running, dripping and leaking. Find unsafe factors to deal with in time or report to leaders.
班前、班中须检查机器、设备、工具、电气及作业环境的安全情况, 防止跑、冒、滴、漏等危险情况的发生。发现不安全因素及时处理或向领导汇报。
- Careful implementation of the succession system, the succession must be carefully checked before the position of equipment and safety facilities are intact.
认真执行交接班制度,接班前必须认真检查本岗位的设备和安全设施是否齐全完好。
- Comply with HSE rules and regulations and obey management.
遵守HSE规章制度和操作规程,服从管理。
- Correct wear and use of labour protective equipment.
正确佩戴和使用劳动防护用品。
- Accept HSE education and training, participate in emergency drills, master the safety knowledge needed by their work, improve safety prevention skills, enhance accident prevention and emergency response capabilities.
接受HSE教育和培训,参加应急演练,掌握本职工作所需的安全知识,提高安全防范技能,增强事故预防和应急处理能力。
- If any hidden danger or unsafe factor is found, it shall immediately report to the HSE management personnel or the person in charge of the company.
发现事故隐患或者不安全因素,应当立即向现场HSE管理人员或者公司负责人报告。
- Participate in the daily + QDCI meeting, in accordance with the requirements of HSE8, fill in and feedback all kinds of HSE problems timely and correctly, and actively implement rectification.
参加每天+QDCI会议,结合HSE8要求,及时、正确填写和反馈各类HSE问题,并积极落实整改。
- When a production safety accident emergent, it will obey the unified command at the scene.
发生生产安全事故紧急撤离时,服从现场统一指挥。
- Comply with accident investigation and provide relevant information faithfully.
配合事故调查,如实提供有关情况。
- Those who engage in special operations are specially trained to get special assignments.
从事特种作业的,经过专门培训取得特种作业资格。
- Occupational health qualifications: Occupational disease protection equipment and occupational disease protection articles for personal use should be regularly maintained and overhauled, their performance and effect should be regularly tested to ensure that they are in a normal state and may not be dismantled or stopped using without authorization. Learn and master the relevant occupational health knowledge, abide by the laws, regulations, rules and operating rules of occupational disease prevention and control, correctly use and maintain occupational disease protection equipment and occupational disease protection articles for personal use.
职业健康资格:对职业病防护设备和个人使用的职业病防护用品,应当进行经常性的维护、检修,定期检测其性能和效果,确保其处于正常状态,不得擅自拆除或者停止使用。 应当学习和掌握相关的职业卫生知识,遵守职业病防治法律、法规、规章和操作规程,正确使用、维护职业病防护设备和个人使用的职业病防护用品。
· Energy saving General:
- Support the development of energy-saving projects and give positive feedback.
支持节能项目的制定,积极反馈意见。
- Participate in and implement energy-saving projects.
参与并实施节能项目。
- Participate in and implement ISO50001 qualify.
参与并实施ISO50001认证
· Quality requirements
- Report product complaints and adverse drug reactions according SOP requirements.
根据SOP要求报告产品投诉和药物不良反应。
- Participate in and complete personal training on time.
按时参加并完成个人培训。
- Operate in accordance with SOP standards.
按照SOP标准要求进行操作。
- Fill in GMP documents and records in accordance with SOP standards.
按照SOP要求填写GMP文件和记录。
- Report abnormal conditions in a timely manner.
及时汇报异常情况。
- Perform activities related with Medical Device according to the current Good Supply Practice (GSP) regulations.
依据现行经营管理规范(GSP)执行医疗器械相关活动”
About you 任职资格:
Pursue progress, discover extraordinary进无止境,探索菲凡
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
进步,外部可见。更好的药物,更好的效果,更高的科学。但是进步离不开人去创造——来自不同背景、不同地区、担任不同岗位的人。所有人都团结在“创造奇迹的渴望”这一使命下。让我们成为这样的人。
在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。
观看我们的 ALL IN 视频,并在 sanofi.com 网站上查看我们有关多元化、公平性、包容性的举措。