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更新于 7月8日
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CMC PM(J21804)

2.5-4萬·14薪
  • 上海浦東新區(qū)
  • 5-10年
  • 碩士
  • 全職
  • 招1人

職位描述

醫(yī)藥研發(fā)項目
崗位職責:
1.Client Liaison: Serve as the primary point of contact for the client, answering questions about company capabilities and ensuring client satisfaction throughout the project lifecycle to secure more business opportunities in the future.
2.Project Coordination: Coordinate all project activities from proposal to delivery, addressing client concerns about deliverables to ensure revenue recognition.
3.Meeting Coordination: Organize meetings, prepare agendas and minutes for clients, and timely follow-up on the action items identified during the meetings.
4.Timeline Management: Monitor project progress according to the Gantt Chart/timeline.
5.Scope Management: Keep track of work scope, liaising with technical leaders and the client to manage scope changes and issue change orders timely.
6.Client Participation: Drive client participation in project tasks, such as document review and knowledge transfer.
7.Problem-Solving and Escalation: Organize internal meetings to find solutions for project issues; escalate unresolved issues or collaboration problems to higher management levels.
8.Crisis Communication: Communicate effectively with the client, minimizing negative impact when unexpected issues arise.
9.Client Visits: Support or host client visits to the company.
任職要求:
1.Education and Experience: The candidate should have a Ph.D. or Master
s degree in organic chemistry or a similar field. They should also have 3-5 years of experience in Contract Research Organizations (CRO), Contract Manufacturing Organizations (CMO), or in the pharmaceutical industry.
2.Training: The candidate should have received training in process development, analysis, Good Manufacturing Practices (GMP) regulations, and production.
3.Cross-Functional Experience: Preference for candidates with experience working across different functions or departments.
4.Communication Skills: The candidate should be excellent in presenting information and communicating in English.
5.Project Management Skills: The candidate should have demonstrated abilities in managing and coordinating projects.
6.Interpersonal Skills: The candidate should have good communication skills, be goal-oriented, and be a team player.

工作地點

上海浦東新區(qū)藥明康德(德林路)

職位發(fā)布者

顧女士/HRBP

剛剛活躍
立即溝通
公司Logo上海合全藥物研發(fā)有限公司
合全藥業(yè)是位于中美兩地的藥明康德集團企業(yè)公司，服務(wù)于生命科學(xué)行業(yè)，擁有卓越的小分子創(chuàng)新藥研發(fā)和生產(chǎn)的能力和技術(shù)平臺。作為全球新藥合作研究開發(fā)生產(chǎn)（CDMO）領(lǐng)域的領(lǐng)軍企業(yè)，合全藥業(yè)致力于為全球合作伙伴提供從小分子原料藥（API）到制劑，高效、靈活、高質(zhì)量的一站式解決方案。合全擁有全球規(guī)模最大的化學(xué)工藝團隊，超過1,000名經(jīng)驗豐富的研究人員和科學(xué)家為您提供全方位的解決方案，包括：合成路線篩選工藝開發(fā)、優(yōu)化和放大確定起始原料、中間體和原料藥（API）的質(zhì)量控制策略工藝驗證我們最先進的生產(chǎn)設(shè)備能夠在cGMP條件下生產(chǎn)從公斤級到噸級的中間體和創(chuàng)新原料藥（API）。巨大產(chǎn)能：上海金山工廠反應(yīng)釜總體積為400m3，常州新工廠將增加反應(yīng)釜總體積1,000m3以上?？傮w我們?yōu)榭蛻籼峁?00個5L-20,000L不同大小的反應(yīng)釜保證生產(chǎn)快速進行。國際標準質(zhì)量體系：上海金山工廠已通過8個全球監(jiān)管機構(gòu)的批準，包括美國FDA、中國CFDA、歐盟EMA、澳大利亞TGA、加拿大衛(wèi)生部、日本厚生勞動省、瑞士藥檢局、新西蘭MPI，工廠可生產(chǎn)創(chuàng)新原料藥（API）和中間體。我們位于上海的制劑基地擁有頂尖的研發(fā)和生產(chǎn)能力，可提供從臨床前到商業(yè)化的制劑研發(fā)，以及用于臨床批次的制劑生產(chǎn)、包裝和貼標服務(wù)，其中包括：和藥明康德的藥物化學(xué)、DMPK以及生物部門合作，進行快速IND開發(fā)。專長于開發(fā)低可溶性藥物和兒科制劑。具備豐富的臨床口服固體制劑的生產(chǎn)經(jīng)驗，生產(chǎn)基地通過美國FDA和瑞典MPA的批準。
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