上海凯莱英生物技术有限公司
QC经理/分析经理
2 months ago
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Important information
Contract type:
Permanent
Location:
Tianjin, China
Work mode:
Onsite
Published on:
8 August 2026
What they need
该职位来源于猎聘 1、负责原料药QC体系构建与维护,统筹原辅料、中间体、成品检验放行,主导OOS/OOT及偏差调查与CAPA,确保数据完整及法规合规; 2、管理团队、设备与预算,配合客户与官方审计,推动方法验证与转移; 3、负责原料药QC体系构建与维护,统筹原辅料、中间体、成品检验放行,主导OOS/OOT及偏差调查与CAPA,确保数据完整及法规合规; 4、管理团队、设备与预算,配合客户与官方审计,推动方法验证与转移; 5、跨部门项目管理,与研发、生产等部门协同推进项目进度; 6、统筹原料药生命周期内的稳定性数据支持,确保放行、变更、申报等流程节点合规高效。 任职资格 1、药学、药物分析、化学等相关专业本科及以上学历; 2、7年以上制药行业QC工作经验,具备团队管理经验优先; 3、熟悉原料药/制剂稳定性研究全流程,具备HPLC、GC、溶出度等分析仪器操作经验。 4、精通ICH Q1系列、中国药典/USP/EP稳定性指导原则; 5、具备审计应对及跨部门沟通协调能力,逻辑清晰,抗压性强;
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