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Location
In office (China)
Confirmed on the employer's own hiring board on Nov 2, 2026. First seen by Alion on Jun 24, 2026. GenScript scores B on the Alion truth index.
Overview
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GenScript is a biotechnology group whose China operations, centred on Nanjing, provide gene and oligo synthesis, peptide, protein, antibody, mRNA and CRISPR services and reagents for life science research and early drug development. The group is listed in Hong Kong and also spans cell and gene therapy and biologics development and manufacturing, as well as industrial synthetic biology that produces enzymes for feed and other industries. Its China teams hire sales managers, project managers with molecular biology backgrounds, validation and facility engineers, procurement and finance specialists, HR business partners and customer data marketing staff.
岗位职责:
1. 负责生产车间及实验室计算机化系统（如HPLC、LC-MS等）的全生命周期日常运维与管理，包括用户账号与权限配置、数据定期检查、转存、介质管理、系统备份/恢复、硬件更换、软件升级及系统退役，确保建立完整的信息档案;
2. 严格遵循GxP及数据完整性规范，监管相关数据合规性，定期执行灾难恢复演练，保障生产与检测数据的安全性与可追溯性;
3. 配合验证团队开展计算机化系统验证（CSV）工作，协助完成系统风险评估、测试脚本执行及相关验证文档的编写;
4. 负责起草、修订及维护 GxP IT 管理与标准操作规程（SOP），确保相关制度持续符合监管要求;
5. 高效完成上级交办的其他专项任务。
任职资格：
1. 大专或本科及以上学历，计算机、信息技术、生物学、药学或自动化等相关专业;
2. 熟悉实验室常用分析仪器（如HPLC、LC-MS、GC等）或生产自动化控制系统的软件及操作流程;
3. 了解GxP规范、计算机化系统验证（CSV）及数据完整性相关法规要求者优先;
4. 具备优秀的学习能力，对合规法规有敬畏心，原则性强，严谨细致;
5. 逻辑清晰，做事情条理性强，能严格按照公司制度与SOP执行工作，具备良好的沟通协调能力和团队协作精神。
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