工作職責:
1. 負責DMPK蘇州/上海實驗室的化合物和生物樣品的全流程管理，包括但不限于：
86 化合物及樣品的接收、分裝、分發、儲存及銷毀
86 確保全流程化合物及樣品的安全性、完整性和可追溯性
2. 對接部門上下游功能團隊，設計并優化化合物及樣品管理流程，提升操作效率與合規性;
3. 制定并持續優化標準操作規程（SOP），識別關鍵人為操作節點（如手工分裝、數據錄入等），建立防差錯機制，強化質量管理體系；
4. 及時應對操作過程中的異常情況，提供合理的解決方案，并推動問題閉環管理；
5. 客戶審計及來訪接待：負責客戶審計的全程支持，確保審計質量；對外展示專業能力，提升客戶信任度；根據審計反饋優化內部流程；
6. 高效完成主管交付的其他任務。
1. Responsible for the end-to-end management of compounds and biological samples across the Suzhou/Shanghai DMPK sites, including but not limited to:
86 Receiving, aliquoting, distributing, storing, and disposing of compounds and samples;
86 Ensuring the safety, integrity, and traceability of compounds and samples throughout the entire process.
2. Collaborate with upstream and downstream functional teams to design and optimize compound and sample management processes, enhancing operational efficiency and compliance.
3. Develop and continuously optimize standard operating procedures (SOPs), identify critical manual operation points (e.g., manual aliquoting, data entry), establish error-proofing mechanisms, and strengthen the quality management system.
4. Promptly address abnormal situations during operations, provide reasonable solutions, and drive closed-loop problem management.
5. Provide full support for client audits to ensure audit quality; demonstrate professional capabilities to enhance client trust; optimize internal processes based on audit feedback.
6. Efficiently complete other tasks assigned by supervisors.
任職資格:
1. 本科及以上學歷，碩士優先；化學、醫藥、生物等相關專業背景；
2. 3年以上醫藥行業實驗室工作經驗；有團隊管理經驗者優先；
3. 具備良好的中英文讀寫能力，可熟練使用英語溝通的優先；
4. 具備快速學習能力及優秀的溝通協調能力，對新技術、新方法保持開放態度，能持續提升專業能力；
5. 具備敏銳的流程優化意識，善于發現問題并提出改進方案，熟悉GLP/GMP規范者優先。
1. Bachelor’s degree or above, with a Master’s preferred; background in chemistry, pharmaceuticals, biology, or related fields.
2. Over 3 years of laboratory experience in the pharmaceutical industry; team management experience is a plus.
3. Proficient in reading and writing in both Chinese and English; ability to communicate effectively in English is preferred.
4. Quick learner with excellent communication and coordination skills; open to new technologies and methods, and committed to continuous professional development.
5. Keen awareness of process optimization, skilled at identifying issues and proposing improvements; familiarity with GLP/GMP standards is preferred.