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