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Technical Document Jobs In Beijing (Peking) - 164 Job Positions Available

1 – 20 of 164 jobs
LSEG jobs

Data Collections Development APAC comprises several teams who are responsible for the development of real-time systems that collect data from stock exchanges in Asia and Pacific; this data is critical to hundreds of thousands of customers

LSEG  22 days ago
Bjak jobs

About A1 There are over 5 billion users using basic applications today such email, notes, tasks that are not AI-native. Our mission is to build a proactive smart assistant for everyday users to bring intelligence to

Bjak  21 days ago
Bjak jobs

About A1 There are over 5 billion users using basic applications today such email, notes, tasks that are not AI-native. Our mission is to build a proactive smart assistant for everyday users to bring intelligence to

Bjak  21 days ago
Master Flo Valve Inc. jobs

Master Flo Beijing Representative office is currently seeking for a full-time Outside or Technical sales manager to be part of the China sales team. Reporting to the China Country manager, this position will be responsible for sales

Master Flo Valve Inc.  7 days ago
Master Flo Valve Inc. jobs

Master Flo Beijing Representative office is currently seeking for a full-time Proposal and Technical Sales Manager to be part of the China sales team. Reporting to the China Country manager, this position will be responsible for proposal,

Master Flo Valve Inc.  7 days ago
Cummins jobs

Job Summary: This applied technology position creates software that is sold as an integral part of Cummins’ products. People in these positions have involvement in identification and understanding of stakeholder requirements and developing specifications, and responsibility

Cummins  4 days ago
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LILT jobs

What You’ll Do Account Management (DTP): Manage DTP requirements for our largest enterprise customers with highly bespoke requirements, requiring in-depth knowledge of the customer and their needs. Quality Management: Oversee account level DTP quality, ensure instructions

LILT  28 days ago
Caterpillar Inc. jobs

Career Area:Strategy Job Description: Your Work Shapes the World at Caterpillar Inc. When you join Caterpillar, youre joining a global team who cares not just about the work we do – but also about each other.

Caterpillar Inc.  28 days ago
AstraZeneca jobs

Head of RIA Clinical Development is a SET‑2 role reporting to the Head of R&D China, accountable for end‑to‑end leadership and delivery of the Respiratory, Immunology, and Infectious Disease clinical portfolios from early development through registration

AstraZeneca  28 days ago
MSD jobs

Job Description Take CMC lead for products under clinical development and for marketed drug products. Coordinate various aspects of CMC regulatory activities with internal and external stakeholders. Act as a primary representative internally and externally for

MSD  27 days ago
Airbus jobs

Job Description: · Perform analysis of the in-service queries / damage reports in aircraft structure received from airline customers / MRO. · Provide repair solutions focusing on design of repair to ensure all airbus standards and

Airbus  26 days ago
Thermo Fisher Scientific jobs

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description Thermo Fisher Scientific Inc. is a premier company that is dedicated to enabling our customers to make the world healthier, cleaner, and safer. We are a team of 100,000+

Thermo Fisher Scientific  26 days ago
BeiGene jobs

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our

BeiGene  26 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

Fortrea  22 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

Fortrea  22 days ago
Fortrea jobs

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

Fortrea  22 days ago
Thermo Fisher Scientific jobs

Work ScheduleStandard Office Hours (40/wk) Environmental ConditionsOffice Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life -

Thermo Fisher Scientific  22 days ago
Thermo Fisher Scientific jobs

Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job DescriptionJoin Us as an Associate Manager Clinical Operations - Make an Impact at the Forefront of Innovation The Associate Manager Clinical Operations oversees the daily line management responsibilities of the

Thermo Fisher Scientific  22 days ago
Mercedes-Benz Group AG jobs

Tätigkeitsbereich:Einkauf Fachabteilung:Procurement China Gesellschaft:Mercedes-Benz Group China Ltd. Standort:Mercedes-Benz Group China Ltd., Beijing Startdatum:01.10.2026 Veröffentlichungsdatum:24.08.2026 Stellennummer:MER00047L0 Arbeitszeit:Vollzeit Bewerben Aufgaben Objectives As the Procurement manager of EE, ADAS & Digital commodity, you will need to demonstrate the performance

Mercedes-Benz Group AG  22 days ago
IQVIA jobs

Job Overview Responsible for performing routine analysis and laboratory testing procedures. Essential Functions • Responsible for performing and documenting analytical procedures in accordance with SOPs and regulatory guidelines. • Performs routine data analysis to determine if

IQVIA  21 days ago

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