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中国ece职位17个。每日更新。
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Clinical Trial Assistant Premium
18小时前
Chengdu, 中国 Parexel 全职When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...
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Site Reliability Engineer Premium
18小时前
Chengdu, 中国 Razer 全职Joining Razer will place you on a global mission to revolutionize the way the world games. Razer is a place to do great work, offering you the opportunity to make an impact globally while working across a global team located across 5 continents. Razer is also a great place to work, providing you the unique, gamer-centric #LifeAtRazer experience that will put...
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DevOps Engineer(英语流利) Premium
3天前
Chengdu, Sichuan, 中国 Syntronic - A Global Design House 全职 ¥25,000 - ¥35,000 临时该职位来源于猎聘 We’re looking for a Cloud Platform Engineer to help us design, build, and maintain secure, scalable cloud platforms that power our business. This is a unique opportunity to play a key role in reshaping our infrastructure, unifying it on AWS, and creating a foundation for innovation and scalability. What You’ll Do Build the...
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FSP CRA I/II(Chengdu/Chongqing/Guiyang)) Premium
2天前
Chengdu, Sichuan, 中国 Fortrea 全职Job Overview: Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. Summary of Responsibilities: Responsible for all aspects of study site monitoring including routine monitoring and...
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医学副总监 (MJ001317) Premium
3天前
Chengdu, Sichuan, 中国 ClinChoice昆翎 全职 ¥35,000 - ¥50,000 临时该职位来源于猎聘 Primary Responsibilities: Responsible for overall clinical research activities for multiple pre- and post-approval studies, evidence generation and dissemination efforts, and budget oversight. Support the design of appropriate clinical trials to meet the clients’ needs Responsible for delivery of assigned clinical programs,...
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FSP CRA I/II(Hefei) Premium
18小时前
Chengdu, 中国 Fortrea 全职Job Overview:Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.Summary of Responsibilities:Responsible for all aspects of study site monitoring including routine monitoring and closeout...
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Technical Support Engineer Premium
18小时前
Chengdu, 中国 Razer 全职Joining Razer will place you on a global mission to revolutionize the way the world games. Razer is a place to do great work, offering you the opportunity to make an impact globally while working across a global team located across 5 continents. Razer is also a great place to work, providing you the unique, gamer-centric #LifeAtRazer experience that will put...
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Software Engineer-Java Premium
18小时前
Chengdu, 中国 Maersk 全职Key Responsibilities1. Design and implement resilient, scalable backend services using Java 17+ and modern frameworks, tailored to logistics use cases such as order fulfillment, shipment tracking, and fleet management. 2. Develop high-throughput APIs and event-driven data pipelines to integrate with logistics-specific systems (OMS, WMS, TMS, GPS trackers,...
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MCU Product Engineer Premium
18小时前
Chengdu, 中国 Monolithic Power Systems 全职Monolithic Power Systems, Inc. (MPS) is one of the fastest growing companies in the Semiconductor industry. We are worldwide technical leaders in Integrated Power Semiconductors and Systems Power delivery architectures. At MPS, we cultivate creativity, are passionate about sustainability, and are committed to provid...
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Technical Support Engineer Premium
2 weeks ago
Chengdu, Sichuan, 中国 Razer Inc. 全职Joining Razer will place you on a global mission to revolutionize the way the world games. Razer is a place to do great work, offering you the opportunity to make an impact globally while working across a global team located across 5 continents. Razer is also a great place to work, providing you the unique, gamer-centric #LifeAtRazer experience that will put...
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(Sr.) Country Study Manager
3 weeks ago
Chengdu, Sichuan, 51, 中国 AstraZeneca 全职**Serve as SDTL** - Responsible for planning and leading the delivery of all components of a clinical study to time, cost, and quality from Study Specifications (SS) through study closeout activities and Clinical Study Report (CSR). - Form a motivated and aligned study team that delivers the study results on or ahead of time and to high quality -...
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DevOps Engineer(英语流利)
3 weeks ago
Chengdu, Sichuan, 51, 中国 Syntronic - A Global Design House 全职该职位来源于猎聘 We’re looking for a Cloud Platform Engineer to help us design, build, and maintain secure, scalable cloud platforms that power our business. This is a unique opportunity to play a key role in reshaping our infrastructure, unifying it on AWS, and creating a foundation for innovation and scalability. What You’ll Do - Build...
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Software Engineer-Java Premium
4 weeks ago
Chengdu, Sichuan, 中国 A.P. Moller - Maersk 远程 全职Key Responsibilities 1. Design and implement resilient, scalable backend services using Java 17+ and modern frameworks, tailored to logistics use cases such as order fulfillment, shipment tracking, and fleet management. 2. Develop high-throughput APIs and event-driven data pipelines to integrate with logistics-specific systems (OMS, WMS, TMS, GPS...
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Software Engineer-Java
4 weeks ago
China, Sichuan, Chengdu, 610041 Maersk Logistics & Services China Limited 全职Key Responsibilities 1. Design and implement resilient, scalable backend services using Java 17+ and modern frameworks, tailored to logistics use cases such as order fulfillment, shipment tracking, and fleet management. 2. Develop high-throughput APIs and event-driven data pipelines to integrate with logistics-specific systems (OMS, WMS, TMS, GPS...
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FSP CRA I/II(Hefei)
4 weeks ago
Chengdu, Sichuan, 51, 中国 Fortrea 全职**Job Overview** Site monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned. **Summary Of Responsibilities** - Responsible for all aspects of study site monitoring including routine...