外審員
5千~1萬/月
工作性質(zhì)全職
職位類別醫(yī)藥研發(fā)/生產(chǎn)/注冊
招聘人數(shù)3人
學(xué)歷要求本科
工作經(jīng)驗3-5年
性別要求不限
用工形式不限
技能等級不限
年齡要求不限
試用期無
工作地點(diǎn)泰州醫(yī)藥高新技術(shù)產(chǎn)業(yè)開發(fā)區(qū)/醫(yī)藥城
職位描述
崗位職責(zé)JD：
1、 Conduct external supplier audit as required by the company
按照公司的要求進(jìn)行外部供應(yīng)商審計
2、 Have ability to complete external supplier audit independently after training
經(jīng)過培訓(xùn)后能夠獨(dú)立完成外部供應(yīng)商審計
3、 Conduct pre-audit communication according to audit requirements and make audit arrangements
根據(jù)審計要求進(jìn)行審計前溝通，確定審計安排
4、 Conduct on-site audit according to audit requirements
按照審計要求進(jìn)行現(xiàn)場審計
5、 Adhere to audit requirements, complete audit report, CAPA audit, audit closure and so forth.
按照審計要求完成審計報告、CAPA審核和審計關(guān)閉等工作
6、 Maintain and ensure that suppliers are in approved status
維護(hù)并確保供應(yīng)商處于批準(zhǔn)狀態(tài)
7、 Complete other tasks assigned by leaders
完成領(lǐng)導(dǎo)交代的其他事情
任職需求：
1、 Good English reading and writing skills, fluent oral English is preferred
有較好的英語讀寫能力，有良好的英語口語溝通能力優(yōu)先
2、 At least 2-years working experience in System QA or production process management or QC department management
至少2年以上的體系QA或生產(chǎn)工藝管理或QC部門管理的工作經(jīng)驗
3、 Familiar with GMP or relevant regulations, FDA, EU and other quality related regulations
熟悉GMP或相關(guān)規(guī)定，熟悉FDA，EU等質(zhì)量相關(guān)法規(guī)
4、 Bachelor degree or above in Pharmacology related field
藥學(xué)相關(guān)專業(yè)本科或以上學(xué)歷
5、 Good problem solving and analytical skills
良好的問題解決和分析能力
6、 Good at communication and Decision Making;
良好的溝通技巧和決策能力；
7、 Planning/Organizing with effective Communication Teamwork
通過有效的溝通和團(tuán)隊合作進(jìn)行規(guī)劃/組織
