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更新于 今天

Analytical Development Senior Manager

4.5-6萬
  • 北京朝陽區(qū)
  • 大望路
  • 5-10年
  • 博士
  • 全職
  • 招1人

雇員點(diǎn)評標(biāo)簽

  • 同事很nice
  • 工作環(huán)境好
  • 免費(fèi)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

微生物分析理化分析生化分析藥理毒理分析藥品穩(wěn)定性分析藥品質(zhì)量分析化學(xué)藥
Job description ? Oversee analytical activities for the R&D and commercial portfolio at CROs located in China. ? Provide analytical technical guidance and trouble-shooting support to analytical teams in CRO and other external partners. Review technical documents (protocols/reports) from CRO to ensure GMP compliance. ? Ensure cGMP compliance in all aspects of activities performed at CROs, where relevant. ? Track performance and provide reports on metrics to Management. ? Seek creative approaches to improve the accuracy, reliability, flexibility and productivity of the analytical development activities in China. ? Enhance engagement with Health Authorities to help influencing regulatory landscape in China. ? Closely collaborate in a global environment together with multidisciplinary teams in China, India, US and Europe. Qualifications Education & experience ? You hold a master’s degree in Chemistry, Pharmacy or equivalent with excellent knowledge of analytics, stability and specs. PhD in same fields preferred. ? You have at least 5-8 years of senior level industry experience in global, medium-size pharmaceutical development or research entities or CRO. ? Broad and strong scientific analytical chemistry knowledge in the CMC field, which includes but not limited to analytical method development and validation, GMP release testing, stability study for both API and Drug Product. ? Strong expertise in CMC small molecules early development, with focus on moving compounds from discovery to NME and FIH. Experience with Analytical Development supporting both API and DP is preferred. Experience of working in a matrix environment together with other functions (API, DP, RA, QA, …) to deliver on CMC goals. ? Strong interpersonal skills to effectively communicate with external sites and various internal and external functional areas. ? Good understanding of global Regulatory requirements and ability to respond as to authority questions. ? Ability to prioritize and balance compliance with business needs. ? Experience of microbial testing is a plus. ? Manager experience is a plus. Competencies ? Strong leadership skills are required. ? You can work independently, though you are also an excellent team player. ? Efficient, flexible and dynamic. ? Demonstrate capabilities in strategic thinking ? Sense of Urgency ? Excellent communication skills. ? You have a good knowledge of English, both spoken and written. ? Good English scientific writing skills. ? Chinese language is required for working with local CRO’s.

工作地點(diǎn)

北京朝陽區(qū)華貿(mào)購物中心

職位發(fā)布者

李女士/HR

當(dāng)前在線
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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(yùn)營,擁有19,000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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