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| 部署・役職名 | 【光工場】Project Management Officer (Vaccine Business Unit - Hikari Plant) |
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| 仕事内容 |
タケダでは、常に患者さんを中心に考え、その生活を豊かにするためにイノベーションを推進しています。そして、従業員一人ひとりにそれぞれの能力と熱意に応じた成長の機会を提供することにも取り組んでいます。私たちと一緒に、世界中の人々のいのちに貢献し、さらなる成長と活躍を目指しませんか。 タケダは約5万人の従業員が、80以上の国や地域で働くグローバルな企業です。すべての従業員が世界中の人々の生活をより良いものにしたいという信念をもち、そしてタケダイズム(誠実:公正・正直・不屈)を日々の業務で体現しています。私たちは、240年の研究開発型の製薬企業としての伝統のもと団結し、優れた医薬品の創出を通じて、人々の健康と医療の未来に貢献することをミッションとして掲げています。 About the role: The Manufacturing Project Management, Senior Manager is responsible for planning, organizing, and controlling resources and processes to achieve project objectives within scope, time, quality, and budget constraints. This role involves managing large projects, mentoring junior staff, and developing innovative solutions to complex problems, contributing to Takeda's mission of bringing better health to people and a brighter future to the world. ■OBJECTIVES/PURPOSE ・Lead and manage strategic projects at the site to ensure alignment with VBU (Vaccine Business Unit)’s mission and long-term business objectives. ・Drive successful execution of high-impact initiatives, including: - New product introductions and launch projects - Cross-functional projects involving multiple internal and external stakeholders of VBU Japan - Critical site priorities that advance organizational goals ・Provide expert project management leadership, ensuring effective planning, resource allocation, risk management, and timely delivery of outcomes. ・Collaborate closely with internal and external stakeholders to enable seamless coordination, communication, and alignment across functions. ・Support site strategy implementation by evaluating long-range business plans, translating them into actionable short-term execution plans, and facilitating continuous improvement activities to meet strategic priorities. ・Organize and oversee key events and milestones of VBU Japan, ensuring they contribute to the achievement of strategic goals. ■ACCOUNTABILITIES ・Lead and manage strategic projects at VBU Japan, ensuring alignment with site strategy and VBU priorities while driving measurable improvements in cost, productivity, quality, safety, and compliance. ・Develop and execute project plans, timelines, and resource strategies, incorporating lean principles and continuous improvement methodologies to optimize processes and operational performance. ・Define and monitor Core Value Drivers, KPIs, and operational metrics to ensure effective strategy execution and sustained business impact. ・Foster strong collaboration and communication with internal and external stakeholders, ensuring risk management, compliance, and successful delivery of key site initiatives ■DIMENSIONS AND ASPECTS <Technical/Functional (Line) Expertise> ・Proven project management expertise for complex, cross-functional initiatives. ・Certification or strong knowledge of project management methodologies (PMP, PRINCE2, AGILE). ・Proficiency in project management tools (MS Project, Smartsheet, or equivalent). ・Proficiency in risk management, planning, and resource allocation for strategic projects. ・Competence in data analytics and reporting tools for project performance tracking. ・Familiarity with change management principles to support smooth implementation ・Understanding of cGMPs, regulatory standards, and compliance requirements. <Leadership> ・Builds alignment and engagement across diverse teams and stakeholders. ・Influences decision-making and drives collaboration at all organizational levels. ・Coaches project teams to deliver results and fosters accountability. <Decision-making and Autonomy> ・Leads critical projects addressing strategic priorities with minimal supervision. ・Makes timely decisions on scope, resources, and risk mitigation to ensure success. <Interaction> ・Communicates effectively with internal and external stakeholders, including senior leadership. ・Provides transparent reporting on KPIs, timelines, and project progress. <Innovation> ・Identifies opportunities for process improvement and efficiency within project scope. ・Leverages digital tools and AI/automation where applicable to optimize project delivery. <Complexity> ・Manages multiple projects simultaneously in a global, cross-functional environment. ・Translates strategic objectives into actionable plans under tight timelines. |
| 労働条件 |
■待遇 ・諸手当:通勤交通費、借家補助費、勤務時間外手当など ・昇給:原則年1回、賞与:原則年2回 ・勤務時間:本社(大阪市中央区・東京都中央区)9:00~17:30、工場(山口県光市・大阪市淀川区)8:00~16:45 、(千葉県成田市)8:30~17:15 、 研究所(神奈川県藤沢市)9:00~17:45 ・休日:土曜、日曜、祝日、メーデー、年末年始など(年間123日程度) ・休暇:年次有給休暇、特別有給休暇、傷病休暇、ファミリーサポート休暇、産前産後休暇、育児休暇、子の看護休暇、介護休暇 ・働き方関連制度:フレックスタイム制、テレワーク勤務制導入(対象社員) ・福利厚生: 社会保険制度、退職金・企業年金制度、従業員持株制度等 ■労働条件に関する重要事項 業務内容については入社後に会社の定める業務への変更もあり得ます。 配属先および就業場所に関しては、入社後に会社の定める部署および就業場所への変更もあり得ます。 ■Locations 山口 |
| 応募資格 |
【必須(MUST)】 ・Bachelor’s degree strongly preferred concentration in technology, manufacturing/operations, or an equivalent level of degree.・Demonstrated experience with project management ・Excellent interpersonal and communication skills in both English and Japanese ・Demonstrated success in applying to commercial, transactional, or manufacturing process improvement tools. ・High energy, team oriented, data driven, and results focused. ・Excellent interpersonal, written, verbal communication skills and organization skills must be comfortable teaching and presenting to large groups at all levels of ・the organization from shop floor to Plant head and region head. ・Strong analytical and problem-solving skills with a data-driven mindset. ・Demonstrated accountability for delivering high-quality results on time. ・Proficiency in project management software (MS Project, Smartsheet) and data analytics tools (Power BI, Tableau). ・Strong skills in risk management and change management frameworks. ・Ability to manage external vendors and global stakeholders effectively. 【歓迎(WANT)】 ・5+ years of experience supporting manufacturing and/or CMC activities・Business acumen and commercial awareness in Pharma ・Strong business acumen and commercial awareness in pharmaceutical industry ・Demonstrated commitment to diversity, equity, and inclusion (DE&I) in the workplace. ・Project Management Certification (PMP, PRINCE2, or AGILE) preferred. ・Some international travel will be required. ・This job description is not designed to be a complete list of all duties and responsibilities required of the position. |
| アピールポイント | 自社サービス・製品あり 日系グローバル企業 女性管理職実績あり 上場企業 従業員数1000人以上 創立30年以上 年間休日120日以上 産休・育休取得実績あり ストックオプション制度あり 教育・研修制度充実 資格支援制度充実 完全土日休み フレックスタイム |
| リモートワーク | 可 「可」と表示されている場合でも、「在宅に限る」「一定期間のみ」など、条件は求人によって異なります |
| 受動喫煙対策 | 屋内禁煙 |
| 更新日 | 2026/01/23 |
| 求人番号 | 6621592 |
採用企業情報
- 武田薬品工業株式会社
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- 資本金1,676,200百万円
- 会社規模5001人以上
- 医薬品メーカー
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会社概要
【設立】1925年1月29日
【代表者】クリストフ・ウェバー
【資本金】1兆6,762億円 ※2022年3月末時点
【従業員数】5,149名 ※2022年3月末時点
【本社所在地】東京都中央区日本橋本町二丁目1番1号
【その他事業所】大阪、神奈川、山口、千葉、京都
【事業内容】医薬品等の研究開発・製造・販売・輸出入
転職・求人情報の詳細をご覧になる場合は会員登録(無料)が必要です