Technical Writing Jobs in Shanghai

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 aspects of study s...

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are our expertise in Innovative Medicine and MedTech we are unique...

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 of project plans as assigned. Function as...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre 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...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

Job OverviewPrepare analysis plans and write detailed specifications for analysis files tables listings and figures. Interpret analyses and write statistical sections of study reports. Provide training guidance and mentorship to lower level and new staff.Essential Functions Production of High-Qualit...

TERADYNE where experience meets innovation and driving excellence in every connection. We are fueled by creativity and diversity of thought and in our workforce. Our employees are supportedto innovate and learn something new every day.We cultivate a culture of inclusion for all employees that respec...

The Application Specialist will be responsible for offering product expertise application knowledge and technical support along each step of customers process and for bringing the products technical expertise and market knowledge to the sales team. The main missions are to ensure successful design v...

PT Engineer Lubrizol Surface Science (LSS)Background:The Process Technology Engineer supports product commercialization from initiation through first production collaborating across diverse teams and working with third-party manufacturers. Main responsibilities include providing operations input to...

Background:The Process Technology Engineer plays a key role in leading product commercialization from initial concept through first production partnering closely with cross-functional teams and third-party manufacturing partners. This position is responsible for providing operational expertise to en...

At Cadence we hire and develop leaders and innovators who want to make an impact on the world of technology.Principal Analog Design EngineerJob SummaryThis role could be based in Shanghai or Nanjing and recognized as an analog design expert demonstrating substantial development & business impact by...

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibilities for clin...

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 aspects of study s...

At Cadence we hire and develop leaders and innovators who want to make an impact on the world of technology.ResponsibilitiesResearch and develop advanced algorithms for Signal Integrity (SI) analysis and Circuit Simulation EDA.Research and develop algorithms for system-level network modeling and sim...

Company OverviewKLA is a global leader in diversified electronics for the semiconductor manufacturing ecosystem. Virtually every electronic device in the world is produced using our technologies. No laptop smartphone wearable device voice-controlled gadget flexible screen VR device or smart car woul...

Job OverviewActs as Lead Medical Writer on more advanced writing projects (e.g. complex clinical study reports protocols more challenging indications or customers). Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the a...

Youll be part of a vibrant team dedicated to upholding the quality of Apples first-party Inductive charging products. Apply your technical expertise to solve complicated issues collaboratively with cross-functional partners ensuring customer-facing problems are swiftly resolved. Play a pivotal role...

System Integration Test Program Manager Notebooks & DesktopsDescription -Job Summary This role is responsible for leading system integration test programs across notebook and desktop product lines managing cross-functional engineering and validation teams. The role applies advanced technical and pro...