• 无工作经验
  • 本科
  • 招1人
  • 12-04 发布
  • 五险一金
  • 免费班车

职位描述

职位描述:  Specific Responsibilities    具体工作职责q Review all Batch Record and ensure all relative document proved in comply with related Baxter Tianjin release standards.回顾批记录并确保所有相关文件均符合天津百特的相关放行标准。q Annual review relative documents for updating as Baxter requirement每年根据百特要求回顾并更新相关的文件。q Annual Product Review cooperating to ensure all elements which required by GMP and Baxter Procedure are reviewed by relevant department adequately.根据GMP及百特相关程序要求,协调完成产品年度回顾,确保相关部门对各相关章节进行了充分的回顾。q Batch record printing批记录打印工作q Follow up relative quality issues and ensure them completion before finished good released.跟踪相关质量文件确保产品放行前完成。q Observe and monitor behavior, provide feedback for at risk behavior and reinforce safe behaviors in order to prevent accidents.遵守和约束自己的行为举止,对危险行为做出反馈, 加强安全行为,避免事故发生。q Obtain appropriate EHS training and report incidents of noncompliance with EHS laws and requirements or failure to carry out EHS responsibilities, which endanger the environment or people.接受相应的EHS 培训,报告不符合EHS法律的事故或对环境和人员造成伤害的行为。  q Understand and implement Baxter, division and regulatory EHS requirements as applicable to this position.理解并执行百特公司EHS对该职位的相关政策。q Other tasks authorized by Quality Compliance engineer  and / or QA Manager.完成质量经理和质量合规工程师交给的其他任务。 Requirements    职位要求q At least a diploma of college.大专以上学历q Better to have a relative experience.具备相关经历q Good command English.良好的英语水平q Familiar with Pharmaceutical GMP and ISO9000 system.熟悉GMP和ISO9000系统q Good human relationship skills.良好的人际关系技巧  职能类别: 药品生产/质量管理

联系方式

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