應(yīng)屆畢業(yè)生
學(xué)歷不限
最近更新
1538人關(guān)注
職位描述
該職位還未進(jìn)行加V認(rèn)證，請仔細(xì)了解后再進(jìn)行投遞！
工作職責(zé)
* Formulation Testing Team’s task include testing samples of routine,
stability, monitoring, validation and unexpected investigations. Test
supporting work include establishing test procedure, SOP and validation
protocoland report, equipment qualification/calibration maintenance and
consumers management.
* Lead internal and/or external audit on IT system to guarantee the quality
assurance system in compliance with cGMP, international/local regulation, etc..
* As local leader of the ESC project, coordinate headquarters to implement
the project in different relevant Bayer overseas sites. To guarantee the whole
Bayer import products can meet Chinese government regulation, to support the
company’s business development.
* Coordination the compendial coordinator to monitor Chinese Pharmacopoeia
upgrade and follow up decision from RMCA that assure Bayer are in the
compliance position.
* Lead team to give strong technical support to other departments including
Regulatory department and Government affair department.
* To maintain good relationships between BHC and Local authorities by
cooperation with local authorities. Such as Cold Chain, ESC , and computerized
system related workshop.
* Assist QC manager to audit supplier, ensure the audit result truly and
reliable.
任職要求
* Pharmaceutical analysis or related degree of bachelor or above
* At least 8 years working experience inpharmaceutical plant is better
* English in written and reading
* Knowledge on Chinese GMP, Chinese Pharmacopoeia and Europe Pharmacopoeia
* Good operational skills on lab instruments (HPLC, GC, IR, UC etc.);
* Strong team work spirit
* Good communication skill
* Formulation Testing Team’s task include testing samples of routine,
stability, monitoring, validation and unexpected investigations. Test
supporting work include establishing test procedure, SOP and validation
protocoland report, equipment qualification/calibration maintenance and
consumers management.
* Lead internal and/or external audit on IT system to guarantee the quality
assurance system in compliance with cGMP, international/local regulation, etc..
* As local leader of the ESC project, coordinate headquarters to implement
the project in different relevant Bayer overseas sites. To guarantee the whole
Bayer import products can meet Chinese government regulation, to support the
company’s business development.
* Coordination the compendial coordinator to monitor Chinese Pharmacopoeia
upgrade and follow up decision from RMCA that assure Bayer are in the
compliance position.
* Lead team to give strong technical support to other departments including
Regulatory department and Government affair department.
* To maintain good relationships between BHC and Local authorities by
cooperation with local authorities. Such as Cold Chain, ESC , and computerized
system related workshop.
* Assist QC manager to audit supplier, ensure the audit result truly and
reliable.
任職要求
* Pharmaceutical analysis or related degree of bachelor or above
* At least 8 years working experience inpharmaceutical plant is better
* English in written and reading
* Knowledge on Chinese GMP, Chinese Pharmacopoeia and Europe Pharmacopoeia
* Good operational skills on lab instruments (HPLC, GC, IR, UC etc.);
* Strong team work spirit
* Good communication skill
注：聯(lián)系我時，請說是在荊州人才網(wǎng)上看到的。
工作地點(diǎn)
地址：北京朝陽區(qū)北京僑福芳草地大廈
查看地圖
求職提示：用人單位發(fā)布虛假招聘信息，或以任何名義向求職者收取財物（如體檢費(fèi)、置裝費(fèi)、押金、服裝費(fèi)、培訓(xùn)費(fèi)、身份證、畢業(yè)證等），均涉嫌違法，請求職者務(wù)必提高警惕。
職位發(fā)布者
拜耳HR
拜耳醫(yī)藥保健有限公司
-
石油·石化·化工
-
200-499人
-
外商獨(dú)資·外企辦事處
-
經(jīng)濟(jì)技術(shù)開發(fā)區(qū)
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