M&S-Automation Engineer-Beijing
北京, 中国 Fixed Term 发布于 Dec. 02, 2025 申请截止于 Mar. 01, 2026Job title职位名称: Automation Engineer 自动化工程师
- 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:
- 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:
- Minimum of a Bachelor’s Degree in automation / mechanical technology, automation instrumentation or similar disciplines, or equivalent work experience.
自动化、机械、自动化仪器仪表或相关专业,本科及以上学历。
- Previously worked at MNC company and is familiar with Assembling & packaging equipment and processes.
- MNC公司,并熟悉组包装设备及其工艺
- Expertise in DCS, PLC, SCADA, BMS, EMS and HMI systems.
- DCS、PLC、SCADA、BMS、EMS和HMI系统
- Experience in biopharma automation.
- Understanding of ISA-95, ISA-88 standards.
- ISA-95、ISA-88标准
- Problem-solving and project management skills.
Cybersecurity awareness for automation systems
- Good manipulative ability, strong sense of responsibility, good teamwork and communication ability, can solve the problem occurred during the work independently.
良好动手能力,责任心强,良好的团队合作和沟通能力,可以在工作中独立解决问题。
- Languages: Good English writing and communication skills
语言要求: 良好的英语书写及沟通能力
Why choose us?
- Bring the miracles of science to life alongside a supportive, future-focused team.
- Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
- Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
- Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
PursueProgress. Discover Extraordinary.
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. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue progress. And let’s discover extraordinary together.
At Sanofi, we provide equal opportunities to all regardless of race, color, 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!
null追寻 发展。探索 菲凡。
进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。
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 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!
在中国大陆的职位
从新药研究与工程设计到销售环节,我们各部门相互配合,努力实现共同的目标:将新药研发到临床治疗的时间减半。我们为员工铺设非凡的职业发展道路,并为中国大陆市场带来40种创新药物和疫苗。我们还助力国家卫生健康委员会推进“健康中国2030”计划。我们连续四年荣获“中国杰出雇主”第一名的称号。自1982年首次进入中国大陆以来,我们一直追求卓越,不断成长。
体验可能性
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Ama
Ama puts her project management techniques and ServiceNow knowledge to use to help advance Sanofi’s Digital Data operating model. Learn how our team connects data and AI to do what’s never been done before.
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Cambridge Crossing
We're bringing together 2,500 people from across our organization — R&D, Medical, Commercial and Global colleagues all working to realize the power of collaboration.
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Innovation in Action
Our flexible lab of the future will transform how we conduct research, while our innovation center will be fully integrated with existing R&D locations.
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Sanofi’s AI Centre of Excellence in Toronto
The Centre is focused on using leading technologies to develop world-class data and artificial intelligence (AI) products to create value for the health sector.
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Sanofi Canada's Philanthropic Efforts
By chasing the miracles of science to improve people’s lives, we surprise ourselves with what we can achieve. Our team is humbled by the impact our efforts make.
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Sustainable and Green
Our new facility was built to minimize the environmental impact — helping protect our planet and people. Using resources efficiently, we're providing greener, healthier workspaces.
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我们的办公地点
我们的员工遍布60多个国家/地区。他们勠力同心,携手共创医疗健康领域的美好未来。无论您在哪里工作,我们的专家都会指导您推动职业发展,您也将能够运用先进的科学技术,取得意义非凡的重大突破。
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勇敢追梦,奔赴美好未来
想要改变自己的生活,乃至改变全球数百万人的生活,该怎么做?加入我们,开启职业新篇章,然后在我们的保驾护航中展翅高飞,并向优秀的人求教,为这份事业做出切实的贡献。
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您和我们相互依存,共同成长
我们精心打造薪酬体系,为您的身心健康、财务健康与社交健康提供全面保障。我们有着海纳百川的包容性团队文化,无论您在哪个岗位,都能展翅高飞。
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心怀梦想,成就一番事业
我们希望您以饱满的热情投入到自己的工作岗位中,给全球数百万人带来美好生活。您的职业发展道路由您自己来掌控。您只管制定目标,我们会提供充足的培训机会和支持,让您得偿所愿。
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我们的人与文化
我们是首个建立多元化、公平性和包容性(DE&I)委员会的制药企业。我们还建立了“菲常联盟”,为每位员工提供发声的平台。您的声音是我们建设未来道路的重要基石。
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我们的故事
我们关注每一个员工的声音。因为,我们的未来取决于所有员工的付出与努力。正因为他们的助力,我们才能追求远大的理想。
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为什么选择我们?
我们为您提供各种工具、支持和培训机会,帮助您实现自己的目标。我们也希望您充分发挥潜力,帮助我们实现目标:将新药研发到临床治疗的时间减半。