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工作職責(zé)：
1.負(fù)責(zé)GMP相關(guān)文件和記錄的管理工作；
Be responsible for the management of GMP related documents and records
2.負(fù)責(zé)壓縮空氣、氮?dú)赓|(zhì)量檢測(cè)；
Responsible for the quality inspection of compressed air and nitrogen;
3.負(fù)責(zé)對(duì)有關(guān)影響產(chǎn)品質(zhì)量的因素進(jìn)行監(jiān)督，并負(fù)責(zé)問題的糾正、偏差分析處理以及相關(guān)過程的管理及風(fēng)險(xiǎn)管理；
Supervise the factors affecting product quality, and take charge of problem correction, deviation analysis and handling, as well as management and risk management of relevant processes;
4.負(fù)責(zé)現(xiàn)場(chǎng)質(zhì)量監(jiān)督工作及潔凈室環(huán)境監(jiān)測(cè)工作；
Responsible for on-site quality supervision and clean room environment monitoring;
5.負(fù)責(zé)原輔料、半成品、成品、包裝材料及工藝用水的取樣；
Take samples of raw and auxiliary materials, semi-finished products, finished products, packaging materials and process water;
6.負(fù)責(zé)公司的物料、產(chǎn)品放行，在產(chǎn)品放行前完成對(duì)批記錄的審核，確保每批放行的產(chǎn)品符合相關(guān)法規(guī)、藥品注冊(cè)和質(zhì)量標(biāo)準(zhǔn)；
Be responsible for the release of the company's materials and products, complete the review of batch records before the release of products, and ensure that each batch of products released complies with relevant regulations, drug registration and quality standards;
7.負(fù)責(zé)公司與質(zhì)量有關(guān)計(jì)算機(jī)系統(tǒng)操作權(quán)限的審核。
Be responsible for the audit of the company's computer system operation authority related to quality.
任職要求：
1.有QA工作經(jīng)驗(yàn)者優(yōu)先考慮；
2.大專及以上學(xué)歷；
3.熟練使用計(jì)算機(jī)辦公軟件，熟悉GMP管理要求；
4.善于溝通，工作認(rèn)真仔細(xì)，態(tài)度積極努力
注：該崗位為現(xiàn)場(chǎng)QA，因工作需要跟生產(chǎn)部門出勤時(shí)間保持一致，能接受倒班再行投遞，謝謝！