岗位描述
1. 最低任职要求 Minimum Requirement 教育程度/经验Education background/ Experience 1. 药学、化学、生物工程等相关专业,本科及以上学历; Bachelor or above, major in pharmacy, chemistry, biological engineering or related; 2. 至少2年以上质量管理经验,有生物制药经验优 先; At least 2 years of quality management experience, biological pharmaceutical experience is preferred; 3. 熟悉cGMP、FDA、欧盟等相关法规在质量管理方面的要求。 Familiar with cGMP, FDA, EMA and other related rules and regulations required in quality management 其他要求(比如工作时间或特殊技能等)Other requirements (e.g.: working time, special skills) 1. 具备快速的学习能力;良好的沟通协调能力;优秀的逻辑与决策能力。 Good learning agility;Good communication and coordination;Good logical and decision ability 2. 良好的英语表达技能 Good English presentation skill 3. 周一至周五 08:30-17:00工作段时间;如有工作业务需要,安排时间以 达成工作任务以及紧急情况的处理 08:30 to 17:00 working time from Monday to Friday; and Any time can be planned if any business required
工作职责 Job Responsibility * 1. 负责DS/DP产品生产过程中的现场质量监控和管理 Responsible for site quality monitoring and management during DS/DP product manufacturing 2. 负责相关质量文件的起草、审批 Responsible for drafting and reviewing/approving related quality document 3. 负责DS/DP生产,工程,验证,DI 相 关文件的审核 Responsible for reviewing related documents including DS/DP, Engineering, Qualification/Validation, DI 4. 支持完成DS,DP 批放行相关文件的准备、检查、审核过程 Support completion of preparation, inspection, review process for DS, DP batch release related documents 5. 负责PFD, 主批生产记录(MBR)和批生产记录(BPR)的审核; Responsible for reviewing PFD, MBR, and BPR; 6. 负责处理生产过程中偏差、变更等质量事件; Responsible for handing deviation, change control and other quality events during production 7. 参与项目相关 问题的协调与处理;如兼职QA FL Participate in the coordination and treatment of project related issues, such as part time QA FL 8. 参与公司内审和外审相关工作; Participate in enterprise internal and external audit related work; 9. 开展虫害控制的质量管理 Quality management on pest control 10. 支持MFG22 工厂的GMP 运营 Support GMP running on MFG22 11. 支持 WBS工作 Support WBS projects 12. 领导安排的其他工作。 Other work assigned by the leader.