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大阪府の求人9,641件

CMC Lead, Lifecycle Management, Small Molecules

給与
記載なし
勤務地
大阪府
休日
年間休日123日
雇用形態
正社員

どんな仕事かAIによる生成

Provides operational and tactical leadership for CMC lifecycle management of commercial products in Takeda's small molecule portfolio. Leads CMC teams and lifecycle management strategies, coordinates across GSQ and other functions, and supports lifecycle decisions, manufacturing innovation, and team development.

応募資格・募集要項・仕事内容を見る

この求人に応募

給与記載なし

募集元で応募する武田薬品工業株式会社の採用ページへ
相談する共有準備中

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応募資格

必須

  • A bachelor's degree in engineering or life sciences.
  • Minimum 8 to 12 years of experience in pharmaceutical development and manufacturing, including post-approval lifecycle management.
  • Experience defining and leading the strategy and roadmap for cross-functional initiatives.
  • Proven ability to analyze and solve complex problems through innovative thinking, experience, and project management tools.
  • Scope includes leading innovation in manufacturing equipment, manufacturing processes, and use of digital technology to enable data-driven approaches.

歓迎

  • Demonstrated success operating in a global, matrixed organization preferred.

求める人物像

  • Strategic thinking, with a focus on serving patients and building trust.
  • Creating an environment that inspires and enables people.
  • Focusing on key priorities and delivering strong results.
  • Building capabilities for now and the future.

募集要項最終確認 10/24

職種
製造業
雇用形態
EmployeeRegularFull time
役職
Associate Director
給与
記載なし
給与の詳細
Salary Increase: Annually, Bonus Payment: Twice a year
手当
CommutationHousingOvertime Work
勤務地
大阪府Osaka
働き方
Flexible Work Styles: Flextime, Telework
勤務時間
Working Hours: Headquarters (Osaka/ Tokyo) 9:00-17:30, Production Sites (Osaka/ Yamaguchi) 8:00-16:45, (Narita) 8:30-17:15, Research Site (Kanagawa) 9:00-17:45Flextime
年間休日
123日
休日・休暇
Saturdays, Sundays, National Holidays, May Day, Year-End Holidays etc. (approx. 123 days in a year)Annual Paid LeaveSpecial Paid LeaveSick LeaveFamily Support LeaveMaternity LeaveChildcare LeaveFamily Nursing Leave
福利厚生
Retirement and Corporate Pension, Employee Stock Ownership Program, etc.
社会保険
Social Insurance
業務の変更の範囲
It is possible the job scope may change at the company’s discretion.
就業場所の変更の範囲
It is possible the department and workplace may change at the company’s discretion.
経験年数
8年以上
学歴
大学卒業以上
掲載日
2026/10/16 09:15(8日前)
最終確認
2026/10/24 01:35(今日)

仕事内容

About the role:

  • As an Associate Director, CMC Lead, LCM, Small Molecules, you will provide operational and tactical leadership for the CMC lifecycle management of commercial products within Takeda's small molecule portfolio. You will act as a key CMC interface between Pharmaceutical Sciences, Global Supply & Quality (GSQ), and manufacturing technology organizations, supporting scientific excellence, sound lifecycle stewardship, and effective resource utilization across competing priorities. You will lead CMC teams responsible for the CMC content of commercial small molecule products, and help prioritize lifecycle management and technology excellence activities to optimize resource use across the portfolio.

How will you contribute:

  • Lead cross-functional GSQ CMC teams to support lifecycle management activities.
  • Shape and drive the execution of robust lifecycle management strategies for Takeda's commercial small molecule assets.
  • Serve as the CMC representative for assigned products within Takeda's Global Product Teams under the guidance of senior CMC leadership.
  • Own key CMC decisions within your scope, making recommendations that directly influence lifecycle and supply outcomes, and escalating decisions with broad cross-portfolio impact
  • Resolve complex CMC issues for assigned products, coordinating with cross-functional teams toward solutions and escalating enterprise-level issues to senior leadership with clear recommendations
  • Lead initiatives across GSQ functions, including internal and external manufacturing sites, to advance robustness, technology excellence, and innovation, including digital solutions and data analytics.
  • Brings deep expertise in small molecule manufacturing, the regulatory environment, lifecycle management, post-approval changes, innovation trends, and financial fundamentals.
  • Partner with Project Managers to support the success of the CMC team.
  • Shape and recommend decisions regarding the ongoing lifecycle management of the marketed SM asset, exercising autonomy within defined scope
  • Lead and oversee Lifecycle Management activities, coordinating SMEs across functional areas.
  • Drive alignment across the MSAT small molecule organization (including API and DP) to align LCM activities across GSQ functional organizations.
  • Partner with the MSAT CMC Launch group to ensure a smooth transition of products from launch into ongoing lifecycle management.
  • Mentor and develop CMC team members and contribute to building organizational capability.

この求人は、武田薬品工業株式会社の採用ページの内容をAIが読み取って整理したものです。応募の前に採用ページの原文を確かめてください。データの集め方企業サイト

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