Qa 工作 在 Chengdu

Ready to take your career global? Make your mark at one of the biggest names in payments. We’re looking for a Performance QA Engineer to join our engineering team and help shape the future of global commerce. In this role, you’ll play a key part in building and evolving our shared performance testin

康诺亚生物医药科技(成都)有限公司

该职位来源于猎聘 职责描述： 1. 生产现场监督：对本公司原液生产过程进行监控，包括细胞库建库、原液生产（细胞培养和纯化）过程的关键操作环节进行监控；执行关键生产过程的动态环境监测。 2.对批记录/相关辅助记录进行符合性审核。完成电子数据审核。 3. 对原液车间相关文件（工艺规程/批记录/管理文件/操作规程）进行新增和修订内容的审核。 4.参与并追踪车间的质量事件（变更/偏差/CAPA/OOS/OOT/MDD)。 任职要求： 学历：本科学历 专业：生物制药及药学相关专业 工作经验：有药企生产/QA实习经验优先；熟悉GMP、中国药典、药品管理法、ICH等法规。具有较好的沟通和协调能力。

Performance QA Engineer Ready to take your career global? Make your mark at one of the biggest names in payments. We’re looking for a Performance QA Engineer to join our ever-evolving technology team and help shape the future of global commerce. What you’ll own Own the architecture and technical roa

Responsibility: • Participate in the entire development life cycle including: requirement analysis, driving the testing from planning to completion, designing good test cases with high coverage, testing web service and application, tracking defects with meaningful details, providing root cause analy

Joining Razer will place you on a global mission to revolutionize the way the world games. Razer is a place to do great work , offering you the opportunity to make an impact globally while working across a global team located across 5 continents. Razer is also a great place to work, providing you th

Every day, Global Payments makes it possible for millions of people to move money between buyers and sellers using our payments solutions for credit, debit, prepaid and merchant services. Our worldwide team helps over 3 million companies, more than 1,300 financial institutions and over 600 million c

康诺亚生物医药科技(成都)有限公司

¥14,000 - ¥19,000 /月

该职位来源于猎聘 职责描述: 1 体系与策略：建立、维护并持续优化公司的计算机化系统验证生命周期管理体系和相关SOP，确保其符合cGxP、21 CFR Part 11、EU Annex 11、GAMP 5等法规和指南的要求。 2 团队管理：领导和管理CSV团队，包括任务分配、工作指导、绩效评估和团队成员的专业发展。 3 项目管理：主导关键GxP计算机化系统（如LIMS, ERP, MES, QMS，临床数据管理系统等）的验证项目，制定验证策略和主计划，确保项目按时、按质、合规完成。 4 验证活动监督： 审核和批准关键的验证文件，包括验证计划、用户需求说明、风险评估、验证方案（IQ/OQ/PQ）