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更新于 5月21日

BAS-中心試驗室檢驗科專家

2-3萬
  • 上海浦東新區(qū)
  • 經驗不限
  • 本科
  • 全職
  • 招1人

雇員點評標簽

  • 工作環(huán)境好
  • 同事很nice
  • 團隊執(zhí)行強
  • 氛圍活躍
  • 人際關系好
  • 免費班車
  • 交通便利
  • 非常鍛煉人

職位描述

分析
崗位職責:
1.Be responsible for the technical and scientific oversight of the laboratory·
2.Manage and supervise laboratory tests following for safety lab testing, including but not limited to hematology, chemistry, urinalysis, coagulation, microbiology, immunology, flow cytometry, etc..
3.Create/update SOP following the CAP, CLIA, GLP regulations.
4.Oversee the quality of central lab performances.
5.Project management of clinical trials in central laboratory.
6.Work with company project manager or BD person to bid on projects.
7.Participate in TC with clients for any lab related issues.
8.Talent training and retention
9.Other tasks assigned by Dept. leader.
任職要求:
1.At least bachelor
s degree or above in a medical technology, medical technology from an accredited institution. Licensed to practice in a medical/safety/pathology laboratory, with at least intermediate-level professional certificate. MD or DO in medical testing field is preferred.
2.Strong background in validating or transferring clinical tests.
3.At least 8 years of working experience in CRO industry and CAP or CLIA accredited Laboratory, with rich experience in coagulation testing and microscopic examination in hemanalysis and urinalysis testing.
4.Fluent in both English and Chinese.

工作地點

浦東新區(qū)中國上海外高橋自貿區(qū)富特中路288號

職位發(fā)布者

劉先生/資深人力資源

三日內活躍
立即溝通
公司Logo藥明康德新藥開發(fā)有限公司
藥明康德(股票代碼:603259.SH/2359.HK)為全球醫(yī)藥及生命科學行業(yè)提供一體化、端到端的新藥研發(fā)和生產服務,在亞洲、歐洲、北美等地均設有運營基地。藥明康德通過獨特的“CRDMO”業(yè)務模式,不斷降低研發(fā)門檻,助力客戶提升研發(fā)效率,為患者帶來更多突破性的治療方案,服務范圍涵蓋化學藥研發(fā)和生產、生物學研究、臨床前測試和臨床試驗研究等領域。2024年,藥明康德連續(xù)第四年被MSCI評為ESG(環(huán)境、社會及管治)AA級。目前,公司的賦能平臺正承載著來自全球30多個國家約6,000家合作伙伴的研發(fā)創(chuàng)新項目,致力于將更多新藥、好藥帶給全球病患,早日實現“讓天下沒有難做的藥,難治的病”的愿景。
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