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更新于 5月14日

PM/項(xiàng)目管理

8000-15000元
  • 武漢江夏區(qū)
  • 經(jīng)驗(yàn)不限
  • 本科
  • 全職
  • 招1人

職位描述

生物工程醫(yī)藥制造
Job Responsibilities 工作職責(zé): 1.Responsible for project lifecycle management, project schedule tracking and maintenance, project communication and coordination. 負(fù)責(zé)項(xiàng)目全生命周期管理、項(xiàng)目時(shí)間表的跟蹤及維護(hù)、項(xiàng)目溝通協(xié)調(diào)工作; 2.Coordinate with various departments internally, organize internal CMC meetings regularly, follow up the progress and completion of action items, and ensure the smooth implementation of each project. 對(duì)內(nèi)協(xié)調(diào)各部門(mén),定期組織內(nèi)部CMC會(huì)議,跟蹤進(jìn)度及行動(dòng)項(xiàng)的完成情況,保障各項(xiàng)目順暢執(zhí)行; 3.Communicate with the customer externally, coordinate and manage the problems of both sides in the customer project and give timely feedback to the internal departments. 對(duì)外與客戶(hù)溝通,對(duì)客戶(hù)項(xiàng)目中雙方的問(wèn)題進(jìn)行協(xié)調(diào)管理及及時(shí)的反饋給內(nèi)部各部門(mén); 4.Responsible for project implementation management, find and deal with problems in project development, organize project team members to conduct research, and put forward reasonable solutions. 負(fù)責(zé)項(xiàng)目執(zhí)行管理,發(fā)現(xiàn)和處理項(xiàng)目開(kāi)展中的問(wèn)題,組織項(xiàng)目組成員進(jìn)行研究,并提出合理性解決方案; 5.In the process of writing the project, the minutes of internal and external meetings, the summary of project progress and business letters and other materials. 撰寫(xiě)項(xiàng)目過(guò)程中對(duì)內(nèi)對(duì)外會(huì)議紀(jì)要、項(xiàng)目進(jìn)度匯總及商務(wù)公函等資料; 6.Actively maintain customer relations and maintain a good cooperative relationship between the company and customers. 積極維護(hù)客戶(hù)關(guān)系,保持公司與客戶(hù)良好合作關(guān)系; 7.Assist BD and FA to complete the business work. 協(xié)助BD及FA部門(mén)完成商務(wù)方面的工作; 8.Complete other tasks assigned by superiors. 完成上級(jí)領(lǐng)導(dǎo)安排的其他工作。
Qualification 任職資格: 1.Bachelor degree or above, major in biopharmaceutical or related. 本科及以上學(xué)歷,生物制藥等相關(guān)專(zhuān)業(yè); 2.Bachelor degree more than 5 years, master degree more than 3 years biomedical work experience, at least 1 year project management experience, familiar with biomedical industry, CDMO experience is preferred. 本科五年以上、碩士三年以上生物醫(yī)藥工作經(jīng)驗(yàn),至少一年項(xiàng)目管理經(jīng)驗(yàn),熟悉生物醫(yī)藥行業(yè),具有CDMO經(jīng)驗(yàn)優(yōu)先; 3.Experience in R & D, quality, production, project management, registration, laws and regulations of bio-pharmaceutical companies is preferred. 具有生物藥企研發(fā)、質(zhì)量、生產(chǎn)、項(xiàng)目管理、注冊(cè)、法規(guī)等相關(guān)經(jīng)驗(yàn)優(yōu)先; 4.Have a good sense of service, customer-centered, proactive, result-oriented, hard-working. 具備良好的服務(wù)意識(shí),以客戶(hù)為中心,積極主動(dòng),結(jié)果導(dǎo)向,吃苦耐勞; 5.Have good professional ethics, good organization and coordination, resource integration skills, good at communication, negotiation and public relations. 具有良好的職業(yè)操守,良好組織協(xié)調(diào)、資源整合能力,善于溝通、談判與公關(guān); 6.Strong ability to work independently, strong ability to resist setbacks. 較強(qiáng)的獨(dú)立工作能力, 抗挫折能力強(qiáng); 7.Good English listening, speaking, reading and writing skills. 良好的英語(yǔ)聽(tīng)說(shuō)讀寫(xiě)能力。

工作地點(diǎn)

江夏區(qū)湖北省武漢市東湖開(kāi)發(fā)區(qū)高新二路388號(hào)

職位發(fā)布者

陳女士/HR

剛剛活躍
立即溝通
公司Logo鼎康(武漢)生物醫(yī)藥有限公司
鼎康生物是一家領(lǐng)先的CDMO公司,可提供一站式的CMC解決方案,支持從早期藥物開(kāi)發(fā)到后期臨床研究和商業(yè)化cGMP生產(chǎn)。鼎康引進(jìn)了全球首個(gè)模塊化生物制藥工廠Kubio;為客戶(hù)開(kāi)發(fā)的多個(gè)產(chǎn)品已經(jīng)在全球20多個(gè)國(guó)家進(jìn)行臨床試驗(yàn)。在不久的將來(lái),鼎康生物總產(chǎn)能將超過(guò)140,000L。我們承諾通過(guò)技術(shù)和生產(chǎn)創(chuàng)新,使全球患者都能負(fù)擔(dān)得起具有國(guó)際標(biāo)準(zhǔn)的生物藥物,提高治療水平以改善人類(lèi)健康。
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