- 五險(xiǎn)一金
- 帶薪年假
- 績(jī)效獎(jiǎng)金
VP of GMP Manufacturing
職位描述
? Lead and support tech transfer and manufacturing activities (Cell Culture, Purification and Fill/Finish) for the designated production projects at MFG facility. Serve as CMC leader or single point of contact (SPOC) in the overall CMC team and when interacting with external clients for manufacturing related discussions o Lead the MFGandtech transfer activities including gap analysis, manufacturing process discussion, manufacturing document preparation. o Clearly understand and be responsible to track status of MFG and tech transfer, production progress and technical challenges/achievement of production projects, and make appropriate presentation to clients and management o Ensure client requirements are clearly communicated to production team and management o Write technical and production reports per requirement of the projects assigned o Lead/support for preparation and hosting of regulatory inspection and client/QP audit of MFG for projects assigned o Participate in the review/translation of production batch records, deviation, change control, CAPA and regulatory observation response of projects assigned ? Host client visit and present overview of MFG facility and capability ? Address regulatory observations/audit findings and CAPA of projects assigned ? Participate in PD/QA/QC/AD/MFG technology communication and MFG manufacturing summary, more specifically continuous improvement of o Facility, especially USP/DSP/Fill/Finish system, establishment (including documentation and initial setting up - i.e. IOPQ) o PD/MFG platform technology alignment o Optimization of production execution processes o Reduction of deviations/investigations from technology aspect o Work with various MFG teams (and lead as appropriate) on initiatives including, but not limited to, business process improvements, SOP/MBR template updates, production scheduling optimization etc.
企業(yè)簡(jiǎn)介
公司是一家靈活的全方位生物藥定制研發(fā)生產(chǎn)(CDMO)服務(wù)公司。嚴(yán)格遵照國(guó)內(nèi)外藥品生產(chǎn)管理法規(guī)的質(zhì)量標(biāo)準(zhǔn),包括中國(guó)食品藥品監(jiān)督管理局、美國(guó)食品藥品監(jiān)督管理局(21 CFR)、歐洲藥品局(Eudralex),以及WHO、PIC/S和ICH的標(biāo)準(zhǔn),蘇橋生物致力于為中國(guó)和全球客戶提供臨床前和臨床藥物I期、II期生物藥產(chǎn)品從工藝開發(fā)到規(guī)模化GMP生產(chǎn)的一站式解決方案。服務(wù)類型包含生物藥臨床實(shí)驗(yàn)藥品的工藝研發(fā)、分析方法建立、放大工藝等生物藥下游生產(chǎn)過(guò)程中一系列的全方位服務(wù)!
[展開全文] [收縮全文]職位發(fā)布獵頭
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姓名:劉洪偉
獵頭企業(yè):埃摩森網(wǎng)絡(luò)科技(上海)有限公司
該獵頭其他職位 更多>>
- 100-200萬(wàn)/年 VP of GMP Manufacturing
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