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寡核苷酸/多肽 PM(J21945)

1.8-2.8萬·14薪
  • 上海浦東新區(qū)
  • 5-10年
  • 碩士
  • 全職
  • 招999人

職位描述

多肽寡核苷酸英文流利項目管理經(jīng)驗
崗位職責:
Responsible for managing projects within WuXi TIDES. Leads the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team and business development team. The incumbent will also participate in business development activities such as visiting existing or new clients and promoting WuXi TIDES’ services in conferences/trade shows.
WuXi TIDES, a leading Contract Research and Development Manufacturing Organization (CRDMO), is an integral part of the WuXi AppTec’s subsidiary WuXi STA. WuXi TIDES offers our worldwide partners efficient, flexible, and high-quality solutions for the drug development of oligonucleotides, peptides and related synthetic conjugates (“TIDES” drug). We greatly simplify the TIDES drug development by providing all discovery, CMC development and the entire manufacturing supply chain under one roof.
Essential Functions:
?Lead all project initiation and planning efforts. Participate in the implementation and execution of a given project. Establishes project objectives, timelines and deliverables. Defines project tasks and resource requirements. Closely monitor/control project progression to ensure project is completed on schedule and within budget. Reports project progress to all key stakeholders.
?Supports the technical team to investigate any project challenges by necessary risk assessment tools & techniques, then implements corrective measures.
?Serves as liaison with client contacts, manages day-to-day communications and organizes project team meetings.
?Represents company in project meetings, prepares meeting agenda and minutes, and follows up on action items.
?Evaluates and assesses project results and provides recommendations for future improvements.
?Provides support to the business development team joining customer visits, conferences or tradeshows.
?Facilitates the generation of Quotations/Proposals/Change Orders with inputs from key stakeholders for existing relationships.
任職要求:
Qualifications
Technical Skills / Knowledge:
?Candidate should possess strong and effective project management, problem solving and interpersonal skills and have a proven track record working cross-functionally across a wide variety of technical, business and operational areas.
?Demonstrates good understanding of the pharmaceutical industry and drug development.
?Minimum of 5 years of relevant pharmaceutical or biotech industry experience in discovery chemistry, CMC process development and/or GMP manufacturing.
? Working knowledge and understanding of current regulations and industry trends for oligonucleotide and Solid State Peptide experience is a plus.
? Experience in a Contract Research Organization (CRO) or Contract Manufacturing Organization (CMO) is preferred, but not required.
? Must have working knowledge of MS Office products, especially MS Project.

獎金績效

項目獎金

工作地點

藥明康德(德林路)

職位發(fā)布者

顧女士/HRBP

三日內(nèi)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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