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Bioanalytical Scientist-LCMS(FSP,外派MNC)

2-3萬
  • 上海徐匯區(qū)
  • 虹梅路
  • 經(jīng)驗不限
  • 本科
  • 全職
  • 招1人

雇員點評標(biāo)簽

  • 同事很nice
  • 工作環(huán)境好
  • 免費班車
  • 人際關(guān)系好
  • 團(tuán)隊執(zhí)行強(qiáng)
  • 氛圍活躍
  • 交通便利
  • 管理人性化

職位描述

生物分析高分辨質(zhì)譜大分子
Principle Roles & Responsibilities /Accountabilities 主要職責(zé)/責(zé)任
- Perform hand-on sample preparation for the analysis of selected in vivo and in vitro assay samples (particularly for protein or ADC qualitative and quantitative assays) using LC-HRMS and LC-Triple Quad MS/MS to support discovery programs.
- Perform hand-on sample analysis to profile in-house and competitor compounds including small molecule and large molecule compounds.
- Perform hand-on sample analysis for project specific biomarkers.
- Perform method development and qualification to ensure successful method transfer to CROs for bioanalysis-related activities.
- Perform data analysis and compile method development and sample analysis results. Write study report as needed.
- Conduct hand-on troubleshooting for bioanalytical issues.
Other duties as assigned

Education/Qualifications教育程度/所獲資格證書

● An individual with bachelor or master degree in life science with 0-5 years of working experience.


Key Skill / Knowledge Requirements

● Hand-on experience of bio-sample preparation including plasma, serum, cerebrospinal fluid and tissues. Working experience with regulatory bioanalysis is a plus.
● Training and/or experience with LC-MS/MS is required. Working experience with high resolution mass spectrometry (HRMS), e.g. Thermo Fisher Scientific Orbitrap, is preferred.
● Comfortable to work in a bilingual (English and Chinese) work environment.
● Strong organizational, communicational skills and ability to multi-tasking.
● Self-motivated and engaged learner.
● Experience and knowledge of GxP and regulatory guidance are optional.

工作地點

上海徐匯區(qū)新研大廈

職位發(fā)布者

孫靜/高招TA

三日內(nèi)活躍
立即溝通
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康龍化成(北京)新藥技術(shù)股份有限公司(股票代碼:300759.SZ/ 3759.HK)是國際領(lǐng)先的生命科學(xué)研發(fā)服務(wù)企業(yè)。自2003年成立以來,康龍化成一直致力于人才培養(yǎng)和設(shè)施建設(shè),為包括小分子、大分子和細(xì)胞與基因治療藥物在內(nèi)的多療法藥物研發(fā)打造了一個貫穿藥物發(fā)現(xiàn)、臨床前及臨床開發(fā)全流程的研發(fā)生產(chǎn)服務(wù)體系??谍埢稍谥袊?、美國、英國均開展運營,擁有22,000多名員工,向北美、歐洲、日本和中國的合作伙伴提供研發(fā)解決方案并與之保持良好的合作關(guān)系。(詳情請訪問公司網(wǎng)站:www.pharmaron.com)
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