武田薬品工業株式会社の会社概要

仕事内容

Please note this job requires business level Japanese in speaking, writing, and reading. 【OBJECTIVES/PURPOSE】 ・Work as part of a multi-disciplinary team of computational chemists, medicinal chemists, structural biologists, data scientists, pharmacologists and biologists and provide computational expertise to advance drug discovery projects. ・Contribute to drug discovery efforts across various modalities including small molecules, PROTACs, RNA inhibitors, peptides, and more. ・Implement and execute innovative computational methodologies and tools such as AI, free energy, and cheminformatics approaches to support drug discovery efforts. 【ACCOUNTABILITIES】 Principal Scientist ・Independently design and execute computational strategies for drug discovery projects ・Contribute as a key scientific expert within one or more project teams ・Develop and apply innovative computational methodologies to solve project challenges ・Influence project decisions through data-driven insights ・Mentor junior scientists and contribute to scientific excellence Associate Director ・Provide scientific and strategic leadership across multiple drug discovery projects ・Shape computational chemistry strategies and influence portfolio-level decisions ・Drive adoption of emerging technologies (e.g., AI/ML, generative chemistry) across projects ・Act as a thought leader to project teams and senior stakeholders ・Influence cross-functional teams without direct line management authority ・Mentor and elevate scientific capabilities across the organization 【DIMENSIONS AND ASPECTS】 Technical/Functional (Line) Expertise ・Expertise in a variety of computational tools and methodology including generative chemistry, large-scale virtual screening, molecular dynamics, homology modeling, quantum mechanics, pharmacophore elucidation, data mining, machine learning, cheminformatics and more. ・Significant industry experiences contributing as a computational chemist on drug discovery projects against several therapeutic arias and a variety of drug discovery targets (GPCRs, Kinases, Ion channel etc.). ・Strong impact in progressing discovery projects from hits to clinical leads ・Familiarity with organic and synthetic chemistry concepts. ・Provide project teams with computational strategies to inform, influence, and prioritize designs for potency/selectivity and improve ADME/Tox endpoints. ・Ability to effectively integrate emerging generative chemistry methods and other modern machine learning and artificial intelligence (AI) applications in small molecule drug discovery. ・Proficiency with state-of-the-art Computational Chemistry software. Leadership ・Scientific leadership within project teams ・Mentors junior scientists ・Contributes to method development and innovation ・Influences direction across teams and functions ・Drives innovation and capability building at scale Interaction ・Collaborate with cross-functional global teams ・Present findings to internal stakeholders ・Engage with senior leadership and external partners as needed

仕事内容

【OBJECTIVES/PURPOSE】 ・Ensure compliant GDP export execution by providing operational Quality oversight and expert guidance across export/transportation activities, maintaining inspection readiness and robust documentation. ・Lead risk and quality event management by identifying and mitigating distribution risks, translating QMS requirements into practice, and driving deviations/CAPA and change control for export lanes, providers, and processes. ・Oversee external partners (especially central-contracted distributors) through qualification and performance monitoring, effective Quality Agreements, and strong cross-functional collaboration across Supply Chain, Site Quality, LOC Quality, and project teams. ・As deputy RP responsible Eligible to perform all the duties and have all rights applicable to the Deputy Responsible Person in Singapore as per HSA requirements 【ACCOUNTABILITIES】 ・Provide operational GDP Quality oversight for export execution across shipment preparation, handover, transportation, and delivery, ensuring activities meet applicable GDP regulations and Takeda Quality standards. ・Serve as the Quality SME for export and transportation (including cold chain where applicable), advising on packaging/ship-to configurations, monitoring strategy, handling instructions, security controls, and lane suitability. ・Lead risk identification, assessment, and mitigation for export distribution (lanes, carriers, forwarders, 3PLs, distributors), ensuring risks are documented, owned, controlled, and periodically reviewed in line with governance expectations. ・Oversee deviation/event management for export distribution (e.g., temperature excursions, delays, damages, misroutes, seal breaches), ensuring timely triage, investigation support, documented Quality impact assessment, and effective CAPA implementation. ・Drive change control for export GDP scope, ensuring changes to lanes, logistics partners, distributors, packaging solutions, and monitoring processes are assessed and implemented with appropriate Quality review, evidence, and approvals. ・Deliver GDP oversight of contracted distributors (central Takeda contracts), including distributor qualification/onboarding, Quality Agreement content and maintenance, periodic performance review, escalation management, and ensuring continued compliance with Takeda expectations. ・Ensure compliance with Good Manufacturing Practice and Good Distribution Practice Standards in Singapore ・The company has given authority to the Responsible Person to perform the required activities as per local regulations which include: 　ensuring that an effective quality system is implemented and maintained that meets GDP standard; 　focusing on the management of authorized activities and the accuracy and quality of records; 　ensuring that initial and continuous training prorammes are implemented and maintained; 　coordinating and promptly performing any recall operations for therapeutic products; 　ensuring that relevant customer complaints are dealt with effectively; 　ensuring that suppliers and customers are legally approved or authorized to enable lawful supply of therapeutic products; 　approving any subcontracted activities which may impact on GDP; 　ensuring that self-inspections are performed at appropriate regular intervals following a prearranged programme and necessary corrective measures are put in place; 　keeping appropriate records of any delegated duties; 　deciding on the final disposition of returned, rejected, recalled or counterfeit products; 　approving any returns to saleable stock; ensuring that any additional requirements imposed on certain products by national legislation are adhered to, e.g. controlled drugs. 【CORE ELEMENTS RELATED TO THIS ROLE】 ・Maintain strong cross-functional collaboration with Global Supply Chain, Trade Compliance, Site Quality Organizations, GDC/RDC-related LOC Quality, and Takeda project teams to resolve issues, support initiatives, and ensure aligned decision-making. ・Experience overseeing global export lanes, cold chain distribution, and complex third-party networks. ・Experience with distributor qualification/oversight programs and supplier management. ・Familiarity with global GDP frameworks (e.g., EU GDP guidelines) and practical application across regions. ・Ability to interpret data trends (excursions, lane performance, partner KPIs) to drive risk-based decisions 【DIMENSIONS AND ASPECTS】 ◎Technical/Functional (Line) Expertise ・Demonstrated experience in GDP Quality within pharmaceutical distribution, logistics, or supply chain (typically 5+ years depending on internal leveling). ・Strong working knowledge of GDP expectations for transportation, outsourced distribution, and quality agreements. ・Experience with deviation management, investigations, CAPA, and audit readiness in a regulated environment. ・Understanding of Commercial Quality requirements, including regional and in-country distribution, controlled substance compliance, supply chain quality, and local quality surveillance (returns, recalls, complaints) ◎Leadership ・Ability to collaborate and partner well regionally & cross-functionally with Takeda stakeholder groups and RDCs ・Strong communication skills with ability to influence cross-functional stakeholders and external partners. ・Ability to drive change by influence ◎Decision-making and Autonomy ・Quality approval/endorsement for GDP controls impacting export lanes and distribution models (per Takeda governance). ・Role-specific accountability for Quality oversight of selected distributors and logistics provider ◎Interaction ・Internal: Supply Chain Governance, Global/Regional Quality, Logistics/Transportation teams, Trade Compliance, Planning, Customer Service, Site QA/QP & RP ・External: 3PLs, freight forwarders, carriers, packaging and monitoring suppliers, contracted distributors. ◎Innovation ・Understanding of quality and regulatory requirements and trends related to warehousing and distribution across the global regions.

仕事内容

【募集部門の紹介】 光工場は山口県光市にあるタケダの主力生産工場で、光工場はグローバルの供給ネットワークの中でも重要な基幹工場としての役割を果たしており、出荷先は国内に限らずグローバルに製品を供給しています。 ステライルマニュファクチャリング部は注射剤製造とプロセスサポートの機能を有し、高品質な製品（バイアル製剤、デュアルチャンバーシリンジ）を製造し、継続的なプロセス改善および新規製造ラインの立上げ業務も行うマルチな活動をしている部署になります。 【職務内容】 注射剤の製造工程に関連する以下のような業務を担当していただきます。 ・注射剤製造作業 ・継続的な工程改善 ・適切なSOP整備と教育活動 ・製造工程や設備のバリデーション／クオリフィケーション ・当局の査察の対応 ・新設備、新プロセスの設計と立ち上げ ・デジタル技術など新技術を用いた工程最適化の推進

仕事内容

グローバル化が進む、武田薬品工業にて、ご経験ご希望に応じてポジションを打診させていただきます。 若手〜管理職まで、複数ポジションで案件稼働中。 ＜対象のご経験＞ ・製造 ・生産技術 ・品質管理 ・品質保証 その他、微生物検査などの手技があるなどの方も対象です。 ＝ポイント＝ ・現地への引っ越し費用や借り上げ社宅制度(もしくは住宅手当支給)、引っ越し準備費用の支給など 　スムーズにご入社されるための支援を受けられます。 ・現在積極募集中の工場は「大阪工場」「光工場」です。 　ご希望をお伺いします。 ・「新薬」「他社が真似できない最高レベルの技術を身につけられる」。 ・他医薬品メーカーと比較しても、高水準の処遇レベルが実現可能。

仕事内容

グローバル化が進む、武田薬品工業にて、ご経験ご希望に応じてポジションを打診させていただきます。 若手〜管理職まで、複数ポジションで案件稼働中。 ＜対象のご経験＞ ・製造 ・生産技術 ・品質管理 ・品質保証 その他、微生物検査などの手技があるなどの方も対象です。 ＝ポイント＝ ・現地への引っ越し費用や借り上げ社宅制度(もしくは住宅手当支給)、引っ越し準備費用の支給など 　スムーズにご入社されるための支援を受けられます。 ・現在積極募集中の工場は「大阪工場」「光工場」です。 　ご希望をお伺いします。 ・「新薬」「他社が真似できない最高レベルの技術を身につけられる」。 ・他医薬品メーカーと比較しても、高水準の処遇レベルが実現可能。