Specific Responsibilities????具體工作職責
q?Review all Batch Record and ensure all relative document proved in comply
with related Baxter Tianjin release standards.
回顧批記錄并確保所有相關文件均符合天津百特的相關放行標準。
q?Annual review relative documents for updating as Baxter requirement
每年根據(jù)百特要求回顧并更新相關的文件。
q?Annual Product Review cooperating to ensure all elements which required by
GMP and Baxter Procedure are reviewed by relevant department adequately.
根據(jù)GMP及百特相關程序要求，協(xié)調完成產品年度回顧，確保相關部門對各相關章節(jié)進行了充分的回顧。
q?Batch record printing
批記錄打印工作
q?Follow up relative quality issues and ensure them completion before finished
good released.
跟蹤相關質量文件確保產品放行前完成。
q?Observe and monitor behavior, provide feedback for at risk behavior and
reinforce safe behaviors in order to prevent accidents.
遵守和約束自己的行為舉止,對危險行為做出反饋, 加強安全行為,避免事故發(fā)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.
接受相應的EHS 培訓,報告不符合EHS法律的事故或對環(huán)境和人員造成傷害的行為。??
q?Understand and implement Baxter, division and regulatory EHS requirements as
applicable to this position.
理解并執(zhí)行百特公司EHS對該職位的相關政策。
q?Other tasks authorized by Quality Compliance?engineer ?and / or QA Manager.
完成質量經理和質量合規(guī)工程師交給的其他任務。
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Requirements????職位要求
q?At least a diploma of college.
大專以上學歷
q?Better to have a relative experience.
具備相關經歷
q?Good command English.
良好的英語水平
q?Familiar with Pharmaceutical GMP and ISO9000 system.
熟悉GMP和ISO9000系統(tǒng)
q?Good human relationship skills.
良好的人際關系技巧
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