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Procedures Documentation Jobs In Chengdu - 24 Job Positions Available

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Thermo Fisher Scientific jobs

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to

Thermo Fisher Scientific  25 days ago
Infineon technologies jobs

Senior Engineer Program Management Your role Key responsibilities in your new role Take responsibility for coordinating customer visits including logistics, internal preparation and de-briefing Support team in hosting and documenting customer meetings Support team in articulating

Infineon Technologies  24 days ago
IOTA GROUP jobs

Company Description IOTA GROUP is an international engineering and services company supporting major players in the energy, oil & gas, infrastructure, and industrial sectors. We provide technical expertise and project support through experienced consultants across complex

IOTA GROUP  22 days ago
Cochlear jobs

Cochlear is the global market leader in implant hearing solutions. Cochlears mission is to help people hear and be heard. Around the world, more people chose a Cochlear-branded hearing implant system than any other. A Cochlear

Cochlear  16 days ago
Expeditors jobs

Company Description We take care of our employees, and they take care of our customers! Become a member of a global community! The international logistics industry is an integral piece of the global trade puzzle; we

Expeditors  14 days ago
dsm-firmenich jobs

QC技术员 QC Specialist 四川,成都 Chengdu, Sichuan Assist in developing and maintaining a quality management system to ensure ANH premix products comply with relevant standards and regulations, satisfy customer requirements, meet all legal and regulatory demands, and

Dsm-firmenich  13 days ago
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Fortrea jobs

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

Fortrea  13 days ago
PAREXEL jobs

When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every

PAREXEL  10 days ago
IQVIA jobs

CTA

Essential Functions • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project

IQVIA  10 days ago
Qualcomm jobs

Company: Qualcomm China Job Area:Engineering Group, Engineering Group Software Engineering General Summary: You will design, implement, optimize, and maintain GStreamer plugins for streaming, hardware-accelerated video/audio encoding & decoding, muxing/demuxing, camera integration, GPU/NPU AI inference, and end-to-end

Qualcomm  10 days ago
Airbus jobs

Job Description: CONTEXT OF THE POSITION… As a Planning Intern to support the Planning team, the main activities involve assisting Planning Engineers with long-term schedule preparation, maintaining the material and tooling database, and supporting jobcard preparation

Airbus  8 days ago
Signify jobs

About Signify Through bold discovery and cutting-edge innovation, we lead an industry that is vital for the future of our planet: lighting. Through our leadership in connected lighting and the Internet of Things, were breaking new

Signify  7 days ago
PAREXEL jobs

When our values align, theres no limit to what we can achieve. At Parexel, we all share the same goal - to improve the worlds health. From clinical trials to regulatory, consulting, and market access, every

PAREXEL  7 days ago
Fortrea jobs

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

Fortrea  2 days ago
IOTA GROUP jobs

Company Description Our client is a global multi-energy company operating large-scale refining and petrochemical facilities. It transforms crude oil into fuels and essential industrial products through highly integrated and technologically advanced operations. The organisation is recognized

IOTA GROUP  10 days ago
IOTA GROUP jobs

Company Description Our client is a global multi-energy company operating large-scale refining and petrochemical facilities. It transforms crude oil into fuels and essential industrial products through highly integrated and technologically advanced operations. The organisation is recognized

IOTA GROUP  10 days ago
IOTA GROUP jobs

Company Description IOTA GROUP is an international engineering and services company supporting major players in the energy, oil & gas, infrastructure, and industrial sectors. We provide technical expertise and project support through experienced consultants across complex international

IOTA GROUP  10 days ago
IOTA GROUP jobs

Company Description Our client is a global multi-energy company operating large-scale refining and petrochemical facilities. It transforms crude oil into fuels and essential industrial products through highly integrated and technologically advanced operations. The organisation is recognized

IOTA GROUP  9 days ago
Thermo Fisher Scientific jobs

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more

Thermo Fisher Scientific  20 hours ago

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