工厂质量保证副经理社

面议

上海市本科及以上7年及以上

发布时间：2023-09-06

职位描述

职责描述：
? 负责生产/质量管理有关程序的起草、审核。 Responsible for initial, review of applied procedure of production/quality.
? 负责批生产记录和批检验记录的审核，经授权后释放产品。 Responsible for review of batch record and testing report; responsible for finished product release when authorized.
? 参与各类验证文件的审阅及验证活动的监督。 Review validation documents and conduct supervision when necessary. ? 负责偏差的管理和调查，并负责进行追踪和评估。 Responsible for non-conformance investigation and management, tracking and evaluate CAPA when necessary.
? 负责质量相关客户投诉的调查及监督纠正与预防措施的执行。 Responsible for quality related customer complaint investigation and implantation of CAPA when necessary.
? 负责产品的年度质量回顾。 Responsible for product annual review.
? 负责不合格品的批准和监督处理的执行（如返工、销毁）。 Responsible for reject material and finished products approval, as well as the destruction process.
? 参与内部和外部的审计。 Participate in internal and external audits.
? 遵守环境、安全和健康准则。 Comply with EHS requirements. ?
遵守公司的规章制度和HCC的规定。 Comply with company rules and regulations and HCC policy.
? 有义务按公司投诉程序将客户投诉电话转至相关部门。 Be obliged to transfer the customer complaints to relevant department under customer compliant procedure and involve in the handling of customer complaints if necessary.
? 上级主管交付的其它相关工作 Other wok assigned by supervisor.


任职要求： 本科或本科以上， 药学、化学或其他相关专业，有企业管理背景优先 Bachelor’s degree or above, with pharmaceutical, chemistry or other related major. 五年以上工作经验，熟悉GMP和质量保证体系，具有在制药行业的质量管理经验，了解如何制定质量标准和标准操作程序，有组织和管理能力，对原材料和生产过程控制比较熟悉。 - 5 years above working experience in related industry including the quality management experience in pharmaceutical industry. - Familiar with GMP system. - Strong leadership - Familiar with SOP initiation, review and approval process - Familiar with raw materials and manufacturing control process

其他要求

招聘人数：1人
职能类别：

公司介绍

上海强生制药有限公司诚聘