Introduction

What are you going to do

质量负责人(Quality Head

汇报:COO

工作地点:上海

客户是一家成立于2024年的生物细胞公司,聚焦于‌类器官技术‌与‌诱导多能干细胞(iPSC)‌ 的研发与应用,致力于推动其在‌医药、功能食品、化妆品‌三大领域的转化‌‌。

职责描述:

  1. 质量管理体系搭建及维护
    • 建立、实施并持续优化符合NMPA及药品相关法规标准的体系;
    • 建立、实施食品、化妆品领域的质量体系;
    • 基于公司其它业务逻辑,寻找相应质量参考标准并优化公司体系文件;
  2. 体系文件管理
    • 组织制定、审核并修订所有质量管理相关文件;
    • 业务相关法规政策的识别、传递及培训宣贯;
    • 对文件控制负责;
  3. 体系运行及改进
    • 对公司体系运行的符合性、真实性负责;
    • 对内审进行组织,如定期计划、落实、改进等;
    • 组织第三方外审及相关资质证书申报;
    • 迎接药监或卫健委部门的各类体系检查及缺陷关闭
  4. 质量控制管理
    • 全面负责QC实验室的日常运行管理;
    • 对各类检验任务进行合理安排、分工并确保任务完成;
    • 负责新质控项目的设计及建立,如质量标准、检验方法、物资及委外检测资源等;
    • 对实验室布置布局进行设计、监督实验室现场管理;
    • 各检验任务触发的问题识别、预警、拒收/入库、问题调查分析等;
    • 复核检验数据、记录及台账的准确性、完整性
  5. 质量保证管理
    • 生产过程质量监督,如环境、过程动作、过程记录与要求的一致性判断;
    • 偏差、调查及纠正预防的制定;
    • 对变更的风险进行识别,包括原辅料、工艺、设施设备等,并制定控制措施;
    • 负责各类验证或确认的计划制定、监督落实;
    • 合格供方评定及管理;
    • 产品放行管理,包括出厂放行及放行前对批记录的审核;
    • 不合格品管理,包括不合格的判定、处置及统计分析等;
    • 产品稳定性研究;
    • 以质量视角参与研发工作;
  6. 其它工作
    • 外部对接,如各政府部门法规咨询等;
    • 团队管理及培训
    • 公司交办的其它临时任务

Essential skills and knowledge 

任职要求:

    1. 教育背景: 本科及以上学历, 药学、 生物工程、 制药工程等专业;
    2. 7年药品生产和质量管理的实践经验,3年以上药品质量管理经验;
    3. 熟练掌握质量管理体系,如GMP等相关知识,熟悉生产流程和质量控制方法论。熟悉国内各项《药品管理法》和《药品生产质量规范》等医药生产质量管理相关法律法规;
    4. 英文能作为工作语言。
    5. 除药品外,如有食品、化妆品领域的质量经验为加分项。
    6. 责任心强,善于管理及沟通。

What we offer

Closing: September 20, 2026

Do you have any questions about this vacancy?

Vacancy reference: PR-297662

NZ

Corporate recruiter

Nancy Zhang

+86 21 6072 0285

Contact

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