Manage production in a fast growing China-based studio working with global AAA clients like Disney, Microsoft, Sony, Electronic Arts and Netease. You will be ultimately responsible for the smooth running of all art production and the quality
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
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
Role: Regional Recruitment Manager Location: China – Shanghai / Chengdu / Shenzhen Job type: Full Time, Contract (24 months) Why QS? At QS, we believe that work should empower you. That’s why we foster a flexible
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 timelines.
阅读和分析来自客户的文档,提取关键的技术需求和规格说明,形成内部的检查表 检查3D美术内容,包括模型,贴图,材质等,确保其符合技术规范 制定内部质量控制流程,确保美术团队按照既定的规章制度执行 使用Bug追踪工具来完成Bug生命周期的管理 根据测试结果,定期完成测试报告,并为美术团队总结问题及解决方案 思考和发掘工作中的问题,不断优化和改进质量控制流程 积极与项目组沟通协调,并建立良好关系 Read and analyze documents from clients, extract technical requirements and specifications, and create checklists for the internal team. Inspect 3D assets/content, including models, textures, materials, etc., to ensure they
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
Amazon’s Finance Operations department seeks an Account Payable Analyst for APAC AP operations to join their dynamic group. This analyst is general assigned to handle the expense reimbursements (incl. expense audit, hardcopy filing etc.) and employee
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
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