document controller

中国document controller职位1,000个。每日更新。

  • Electric Part Design Premium

    4小时前


    Hefei, 中国 Volkswagen 全职

    Department Mission• Our department is the central coordinator in China for Thermal Management and Climatization System design and release • We are responsible for Development and Localization for all Audi Projects in China• Our goal as team is to lead and steer all stakeholders to achieve our targets in a friendly and professional working...


  • China 曼德电子电器有限公司 全职

    工作职责1. Optimization of Injection process and manufacture cost, efficiency increase 2. Supports to quality issue 3.Fixture design/specification/ review and improvement of design 4. Supports to new project 5. Standard operation/inspection/internal audit任职要求Education:Bachelor’s degree or above in Mechanical Engineering, Materials, Mold...

  • Application Engineer, Yancheng Premium

    4小时前


    CHN Yancheng - MFG 1 (KUM), 中国 Aptiv 全职

    Major Accountabilities:Conduct value analysis and value engineering activities to optimize product design, improve functionality, and reduce costs.Lead and contribute to the design and development of wiring harness systems for automotive applications.Utilize CAD tools such as CATIA, AutoCAD, and SolidWorks to create detailed wiring harness designs.Manage...

  • On-Site Technical Lead Premium

    4小时前


    Beijing, 中国 Alma Lasers 全职

    Key Responsibilities·      Oversee on-site installation, setup, and operation of production and testing equipment.·      Ensure adherence to defined engineering, safety, and quality standards.·      Coordinate technical and operational activities between local manufacturing, QA, logistics, and the overseas engineering...

  • VMS Global Product Owner Premium

    1天前


    Suzhou Plant Tech Industry Park, 中国 GSK 全职

    Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity.Our trusted portfolio of brands – including Sensodyne®, Panadol®,...


  • Beijing, 中国 Sanofi 全职

    About the jobSanofi has decided to invest into a new large state-of-the art facility for Insulin Drug Substance in Beijing, China. For this green field operation, we’re enhancing our legacy of excellence and build on decades of expertise on the whole value chain of insulin manufacturing. The new facility will be designed as a fully automated, green,...


  • China BASF 全职

    Welcome  If you're someone who inspires others, owns their impact and wants to elevate what they do, you'll fit right in. Until July 1, our business was part of BASF. As part of the current transition, all job listings and the application process are still hosted on the BASF platform and therefore fully presented in BASF branding.Please do not be confused...


  • Guangzhou, 中国 GlobalFoundries 全职

    About GlobalFoundriesGlobalFoundries is a leading full-service semiconductor foundry providing a unique combination of design, development, and fabrication services to some of the world’s most inspired technology companies. With a global manufacturing footprint spanning three continents, GlobalFoundries makes possible the technologies and systems that...

  • Sr. Customer Quality Engineer Premium

    4小时前


    Xiamen, FUJIAN PROVINCE, 中国 Forvia HELLA 全职

    Sr. Customer Quality EngineerLocation Xiamen, ChinaPacesetting. Passionate. Together. HELLA is a listed, internationally positioned automotive supplier operating under the umbrella brand FORVIA. Within this de facto group, HELLA stands for high-performance lighting technology and automotive electronics. At the same time, the Company covers a broad service...

  • Due Diligence Analyst Premium

    4小时前


    Shenzhen, 中国 Arrow 全职

    Position:Due Diligence AnalystJob Description:Do you have an international mindset and interest in global, logistical trade processes? Then Arrow is looking for you! With international shipments constantly coming in and out of our locations you will be a key supporter for the compliance and trade team to ensure regulations are followed and administration is...


  • Guangdong, 中国 Solve 远程 兼职

    Company Description About the Company Join a fast-growing agri-tech company at the forefront of transforming how the world's livestock are managed. As it expands its global footprint, this team is building smart, cutting-edge technology that makes pasture and animal health management smarter, faster, and more sustainable — for farmers everywhere. Job...

  • FSP CRA(Tianjin) Premium

    3小时前


    Beijing, 中国 Fortrea 全职

    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 trials according to Fortrea’s Standard...

  • FSP CRA II Premium

    3小时前


    Shanghai, 中国 Fortrea 全职

    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 trials according to Fortrea’s Standard...

  • FSP CRA II(Guangzhou/Changsha) Premium

    4小时前


    Guangzhou, 中国 Fortrea 全职

    Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interview. If you're pre-selected, our recruiter will keep in touch and let you know when the role officially opens, so we can reconfirm your interest before moving forward with an offerSummary of Responsibilities:Site...


  • Guangzhou, 中国 Fortrea 全职

    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 trials according to Fortrea’s Standard...

  • FSP CRA II Premium

    4小时前


    Beijing, 中国 Fortrea 全职

    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 trials according to Fortrea’s Standard...

  • FSP CRA II Premium

    4小时前


    Chengdu, 中国 Fortrea 全职

    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 trials according to Fortrea’s Standard...

  • Core CRA Premium

    4小时前


    Chengdu, 中国 Fortrea 全职

    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 trials according to Fortrea’s Standard...

  • Fsp Cra II Premium

    4小时前


    Guangzhou, 中国 Fortrea 全职

    Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements, we'll invite you for an interview. If you're pre-selected, our recruiter will keep in touch and let you know when the role officially opens, so we can reconfirm your interest before moving forward with an offer Summary of Responsibilities:Site...


  • Shanghai, 中国 Fortrea 全职

    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 trials according to Fortrea’s Standard...