LyondellBasell is a leader in the global chemical industry creating solutions for everyday sustainable living. With a nearly 70-year legacy that includes a Nobel Prize in Chemistry and our proprietary MoReTec recycling technology, LYB is enabling
Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve health outcomes for people. With our
This position exists to provide end-to-end daily operational coordination and project support for the MPL product. Key responsibilities · Creation and execution of customer shipments according to the implementation plan and customer requirements with regards to
ABOUT QUINCE Founded in 2018, Quince was built to challenge the idea that nice things have to cost a lot. Our mission is simple: to make really high quality essentials for really low prices, produced fairly
公司描述 欧摩威集团于 2025 年9月由大陆集团汽车子集团分拆独立而成。作为一家电子技术与科技公司，欧摩威集团提供广泛的产品组合，致力于让出行安全、愉悦、互联且自主。其业务涵盖传感器解决方案、显示屏技术、制动系统以及舒适系统，并具备软件定义汽车所需的软件、架构平台及辅助系统等全方位技术实力。已归属欧摩威集团的业务领域，在2024 财年实现了196 亿欧元的销售额。集团总部位于德国法兰克福，在全球100多个基地拥有约87,000名员工。 职位描述 Planning and coordinating project deadlines and monitoring progress Defining required deliverables according to the development process, assigning these deliverables to the relevant departments, monitoring progress, and reviewing results Managing
CEVA Logistics provides global supply chain solutions to connect people, products, and providers all around the world. Present in 170+ countries and with more than 110,000 employees spread over 1,500 sites, we are proud to be
Job Description SummaryProduct quality review associated with the manufacturing process. Accountable for the quality of own work. Subject to direct operations supervision/prescribed work instructions/systems checking. Executes within a well-defined operations framework. There is generally a step
We are looking for a detail-oriented and proactive Purchasing Engineer to join our Global Supply team. In this role, you will act as the crucial link between our internal stakeholders and the global supply chain. You
Is accountable for keeping solution documentation and solution data up-to date, approved and stored in the appropriate place: • Approval documents • Authority approval documents • Owner manuals • User manuals • ‘As built’ technical customer
Location(s) Shanghai, Shanghai Company Molex Career Field Quality Job Number 181943 What You Will Do DUTIES & RESPONSIBILITIES: 1.Handle the supplier’s quality issue effectively and timely to protect customers, drive supplier to take containment, corrective and
Job Description Study physician Location: Shanghai Our Company seeks individuals to provide leadership and experience in conducting early clinical research in China. One of the most important missions of clinical research in China is to conduct
JOB DESCRIPTION: 职位目标 Job Purpose: 根据适用的法规、公司政策及风险管理结果建立、落实及完善产品实现过程中的检测体系，确保检验测试活动合规、高效运行。 Establish, implement and improve the inspection and testing system in the product realization process in accordance with applicable regulations, company policies as well as risk management output to ensure all
Location(s) Shanghai, Shanghai Company Molex Career Field Research & Development/Sciences Job Number 189470 Your Job Job Specific intro paragraph Our Team 1-3 sentences to describe the team/division this role will be working in What You Will
Job Description The role is accountable for performance and compliance for assigned protocols and sites in a country. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall
We Offer Joining Maersk, you will become part of the global family of the company that moves 20% of global trade every day all the way, where one of our core values is Our Employees. It
Job title职位名称: China EM&S QA Manager Location工作地点： Shanghai 上海 About the job工作职责 We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company
Typical Accountabilities Support establishing study and trial level V2V process. Support developing V2V related study and trial documents, creating apheresis and product administration manuals and forms and ensure documents are product specific and consistent across all
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical
Labcorp is a leader in diagnostics, drug development and healthcare innovation. Across every role, we harness data and AI to work smarter, move faster and create breakthrough solutions that improve health outcomes for people. With our