应届毕业生
学历不限
2025-04-24 10:18:00
606人关注
职位描述
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工作职责
* 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.
任职要求
* 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.
任职要求
* 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：联系我时，请说是在白云人才网上看到的。
工作地点
地址：北京朝阳区北京侨福芳草地大厦
查看地图
求职提示：用人单位发布虚假招聘信息，或以任何名义向求职者收取财物（如体检费、置装费、押金、服装费、培训费、身份证、毕业证等），均涉嫌违法，请求职者务必提高警惕。
职位发布者
拜耳HR
拜耳医药保健有限公司
-
石油·石化·化工
-
200-499人
-
外商独资·外企办事处
-
经济技术开发区
