更新于 11月20日

PM/項目管理

8千-1.5萬
  • 武漢江夏區(qū)
  • 經(jīng)驗不限
  • 本科
  • 全職
  • 招1人

職位描述

Job Responsibilities 工作職責(zé):
1.Responsible for project lifecycle management, project schedule tracking and maintenance, project communication and coordination.
負責(zé)項目全生命周期管理、項目時間表的跟蹤及維護、項目溝通協(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.
對內(nèi)協(xié)調(diào)各部門,定期組織內(nèi)部CMC會議,跟蹤進度及行動項的完成情況,保障各項目順暢執(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.
對外與客戶溝通,對客戶項目中雙方的問題進行協(xié)調(diào)管理及及時的反饋給內(nèi)部各部門;
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.
負責(zé)項目執(zhí)行管理,發(fā)現(xiàn)和處理項目開展中的問題,組織項目組成員進行研究,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.
撰寫項目過程中對內(nèi)對外會議紀要、項目進度匯總及商務(wù)公函等資料;
6.Actively maintain customer relations and maintain a good cooperative relationship between the company and customers.
積極維護客戶關(guān)系,保持公司與客戶良好合作關(guān)系;
7.Assist BD and FA to complete the business work.
協(xié)助BD及FA部門完成商務(wù)方面的工作;
8.Complete other tasks assigned by superiors.
完成上級領(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,至少一年項目管理經(jīng)驗,熟悉生物醫(yī)藥行業(yè),具有CDMO經(jīng)驗優(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)、項目管理、注冊、法規(guī)等相關(guān)經(jīng)驗優(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,以客戶為中心,積極主動,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.
較強的獨立工作能力, 抗挫折能力強;
7.Good English listening, speaking, reading and writing skills.
良好的英語聽說讀寫能力。

工作地點

湖北省武漢市東湖開發(fā)區(qū)高新二路388號

職位發(fā)布者

Krystal Wang/hr

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,支持從早期藥物開發(fā)到后期臨床研究和商業(yè)化cGMP生產(chǎn)。鼎康引進了全球首個模塊化生物制藥工廠Kubio;為客戶開發(fā)的多個產(chǎn)品已經(jīng)在全球20多個國家進行臨床試驗。在不久的將來,鼎康生物總產(chǎn)能將超過140,000L。我們承諾通過技術(shù)和生產(chǎn)創(chuàng)新,使全球患者都能負擔(dān)得起具有國際標(biāo)準(zhǔn)的生物藥物,提高治療水平以改善人類健康。
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