华领医药技术(上海)有限公司
GMP QA 经理
Skills
3 months ago
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Important information
Contract type:
Permanent
Location:
Shanghai, China
Work mode:
Onsite
Published on:
7 August 2026
What they need
该职位来源于猎聘 工作职责： 原料药、制剂中间产品、制剂产品及临床药物生产受托方生产质量合规管理 负责产品生产记录审核，支持产品放行工作 审核相关的上市后变更、偏差报告，以合规的方式保证产品质量 参与CMOs、供应商质量审计工作 任职资格： 大学及以上相关专业教育背景，系统的完成学习包括药分，药剂，药理，药化制药工程，生物制药等药学基础学科；获得相关学士或者以上学位 熟悉GMP和生产质量管理相关的法规要求 制药行业生产质量5年以上的工作经验 工作积极主动，较强的执行力，沟通能力和逻辑分析能力强
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