Objective of the Programme: The Centre for Nature and Climate (CNC) is a multistakeholder platform that Facilitating cooperation to foster shared prosperity and resilience through climate and nature solutions. The centre helps regional leaders connect with
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
Job Overview: The Senior CRA I is responsible for site monitoring and site management. Responsibility for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The Senior CRA I assure the implementation
About BJAK The original mission of BJAK is we believe people deserve smarter ways to plan, save and grow their money. This is the origin of our name. Started in 2019, we built the first mobile-first
About BJAK The original mission of BJAK is we believe people deserve smarter ways to plan, save and grow their money. This is the origin of our name. Started in 2019, we built the first mobile-first
Location:Beijing, China Job ID: R0138492 Date Posted:2026-07-20 Company Name:HITACHI ENERGY (CHINA) LTD. Profession (Job Category):Administration & Facilities Job Schedule: Full time Remote:No Job Description: The opportunity Hitachi Energy is a global technology leader that is advancing a
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
Senior Management, Payroll & Corporate Secretarial Services 高级经理，薪酬与公司秘书服务 Global Subsidiary Management 全球子公司管理部 Beijing, China 中国北京 Monday – Friday 8:00am – 5:00 pm 周一至周五 上午 8:00–下午 17:00 CSC’s Global Subsidiary Management team is seeking a strategic and
Tätigkeitsbereich:Forschung & Entwicklung incl. Design Fachabteilung:MB.OS Content Management and Rollout Gesellschaft:Mercedes-Benz Group China Ltd. Standort:Mercedes-Benz Group China Ltd., Beijing Startdatum:01.09.2026 Veröffentlichungsdatum:22.07.2026 Stellennummer:MER000469V Arbeitszeit:Vollzeit Bewerben Aufgaben Objective of job Mobile App and OTA Program Management role in
Location:Beijing, China Job ID: R0138457 Date Posted:2026-07-22 Company Name:HITACHI ENERGY (CHINA) LTD. Profession (Job Category):Finance Job Schedule: Full time Remote:No Job Description: The opportunity Hitachi Energy is a global technology leader that is advancing a sustainable
DevOps Engineer WirelessCars Journey WirelessCar empowers the future of mobility by connecting vehicles and delivering cutting-edge digital services. Founded in 1999 and headquartered in Sweden, we have a strong global presence with offices in the U.S.,
AWS Global Sales drives adoption of the AWS cloud worldwide, enabling customers of all sizes to innovate and expand in the cloud. Our team empowers every customer to grow by providing tailored service, unmatched technology, and
Job ID 515467 Posted since 24-Jul-2026 Organization Controlling and Finance Field of work Finance Company Siemens Ltd., China Experience level Experienced Professional Job type Full-time Work mode Office/Site only Employment type Fixed Term Location(s) Beijing -
Role and responsibilities Engineer and implement hardware and/or software solutions for complex part or module failures and other system issues in the China install base. Collaborate with local part supply centers (LPSC), strategic sourcing & procurement (SS&P),
Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put
主要职责Key Responsibilities： 负责银行承兑汇票的签收、背书、台账维护、保管及到期跟踪，确保票据流转安全、记录准确、风险可控； 负责政府及监管部门相关统计和信息报送工作，包括统计局月报、季报、年报，以及商务部外贸外资企业直报信息平台相关外贸调查、信息填报和外汇管理局外币收付款相关报告，协调内部数据收集、复核和解释，确保外部报送质量； 支持北京总公司及上海分公司财政补贴项目申请，包括政策信息收集、申报条件初步评估、申报资料准备、内部数据协调、申请进度跟进及主管部门沟通，提升申报工作的及时性、完整性和成功率； 审核第三方及集团关联公司外币收付款资料，确保支持文件、审批依据及合规要求完整有效，并及时跟进异常事项； 负责应付账款周转率（DPO）报告的数据整理、分析及趋势跟踪，与采购部协作识别付款周期、供应商条款及运营资金改善机会，支持提升公司运营资金使用效率； 负责增值税进项发票认证、勾选、台账维护及相关资料管理，并根据业务需要开具或确认红字确认单，确保税务票据管理准确、及时、合规； 承担中国及香港资金和银行账户相关管理工作，包括现金余额跟踪、资金需求协调、网银账户用户更新与维护、银行印鉴及授权签字人变更流程跟进，确保资金安全、权限管理合规及银行事务高效执行； 管理经销商融资计划，跟进融资资料、额度使用及相关流程执行情况，并与银行、业务团队及内部相关部门保持有效沟通； 参与公司资金规划与现金流预测，支持年度股利分配相关资料准备及流程推进，协助提升资金使用效率和资金管理质量； 与马来西亚财务共享中心（CFS）保持密切协作，围绕应付账款、差旅报销及相关财务运营流程提供本地支持，协调解决流程、系统及异常事项，确保跨区域财务运营流程顺畅、高效、合规运行； 支持差旅报销流程改善，包括流程梳理、问题反馈、员工培训及政策宣导，推动报销流程更加规范、高效； 支持公司内部审计及外部审计工作，包括审计资料准备、数据核对、问题跟进及整改支持，确保审计事项得到及时、准确、合规的响应； 协助完善财务运营相关内部控制流程，确保外部报告、外汇付款、票据及资金管理工作符合公司政策和合规要求； 完成上级交办的其他财务运营、报告及资金管理相关工作。 Manage bank acceptance drafts, including receipt, endorsement, register maintenance, safekeeping, and maturity tracking, ensuring secure circulation, accurate records, and effective
Tätigkeitsbereich:Forschung & Entwicklung incl. Design Fachabteilung:Vehicle Components & Tech Center China Gesellschaft:Mercedes-Benz Group China Ltd. Standort:Mercedes-Benz Group China Ltd., Beijing Startdatum:sofort Veröffentlichungsdatum:03.08.2026 Stellennummer:MER0004658 Arbeitszeit:Vollzeit Bewerben Aufgaben Objective of job Provide effective international delivery and customs solutions
At ABB, we help industries run leaner and cleaner—and every person here makes that happen. You’ll be empowered to lead, supported to grow, and proud of the impact we create together. Join us and help run
Job Overview: The Senior Clinical Research Associate II (Sr CRA II) is responsible and accountable for site monitoring and site management for clinical studies according to Fortrea, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. The