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  3. 武田薬品工業株式会社:Manager, GDP Export Qualityの求人情報詳細

Manager, GDP Export Quality

武田薬品工業株式会社

想定年収

600万円 ~ 1,100万円

勤務地

大阪府

従業員数

5,486名(単体 (連結 49,095名) ※2023年3月末時点)

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

仕事内容変更範囲

会社の指示する業務

職位

募集背景

募集人数

1人

応募条件

技能/経験

・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.

・EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS: 
Scientific Degree (BSc, MSc)
Minimum 10 years experience in in the pharmaceutical industry including Quality Assurance, combined with a good knowledge of regulations pertaining to pharmaceutical manufacturing and distribution in the region (e.g. familiar with cGMP/GDP, ISO and ICH requirements) 
Strong attention to details, ability to review & managing documentation (including transport temperature records, shipping documents, and related GDP documents/ records etc.)
Prior experience managing external GMP/GDP suppliers
Fluent in written and spoken English

・Core Competencies / Skills
Risk-based decision making with strong Quality mindset
Pragmatic operational execution and ownership
Partner management and governance
Clear documentation and inspection readiness discipline
Continuous improvement and problem-solving

・Deliver on Takeda Leadership behaviours
Think Strategically
Inspire others
Deliver  priorities
Elevate Capabilities

学歴

大学

職務経験

不問 (3年以上)

業界経験

年齢

年齢制限不問  

英語力

初級以上

その他語学力

語学力詳細

勤務条件

雇用形態

無期雇用

試用期間

有り(3ヶ月)

給与

月給制

年収:600万円 ~ 1,100万円

月収:31万円~61万円

月額基本給:31万円~61万円

賞与・インセンティブ

年2回  

今までの実績をもとに算出

昇給

有り 年1回 / 4月

勤務地

大阪府

【大阪工場】〒532-8686 大阪市淀川区十三本町二丁目17番85号

交通手段1 沿線名:阪急宝塚線 駅名:十三駅 最寄駅から:徒歩5分

勤務地変更範囲

会社の定める事業所
転勤:当面無し

出向

出向:無し

就業時間

08:00~16:45

休憩時間:60分

残業:月10時間~20時間程度

残業手当

通常の残業代

通勤手当

交通費:全額支給

その他手当

住宅手当

通勤交通費、借家補助費、勤務時間外手当など

休日・休暇

年間休日:123

年間有給休暇:初年度 12日 1か月目から
【休日・休暇詳細】
完全週休二日制(土・日)、祝日、メーデー、年末年始、他
特別有給休暇、リフレッシュ休暇、産前産後休暇、育児休暇、子の看護休暇、介護休暇、フィランソロピー休職制度

社会保険

雇用保険, 健康保険, 労災保険, 厚生年金

福利厚生

社内融資、寮、社宅、社員持株会、財形貯蓄制度、退職金制度

受動喫煙対策

就業場所 全面禁煙

備考

■年収はご経験、現職を考慮の上で決定いたします。 ■選考プロセス詳細は下記の通りです。 ・Web適性テスト、一次面接 → 最終面接(ポジションによって変更あり) ・内定後、リファレンスチェック(履歴の照会)あり。また、卒業証明書、資格の取得証明書等をご提出いただきます。

選考内容

選考プロセス

適性試験:無し 面接回数:2回

求人No.:NJB2375005

最終更新日:2026/4/16

企業情報

企業名

武田薬品工業株式会社

代表者名

代表取締役社長CEO  クリストフ ウェバー

設立

1925年1月

従業員数

5,486名(単体 (連結 49,095名) ※2023年3月末時点)

資本金

ー(1兆6763億円)

本社所在地

〒103-8668 東京都中央区日本橋本町二丁目1番1号

〒540-8645 大阪府大阪市中央区道修町4-1-1

株式公開

プライム

日系・外資

日系

事業内容

医薬品、医薬部外品等の製造・販売・輸出入

事業に関する特色

■日本国内No1企業として、グローバルに活躍する製薬業界のリーディングカンパニー。

■ビジョン2025では、「消化器系疾患(GI)領域でのNo.1、オンコロジー(がん)におけるトップ10、中枢神経系疾患領域および新興国事業での強固なプレゼンス」を長期的な事業の目標としている。

会社の特色

240年を超える長い歴史の中で培われた普遍の価値観である「タケダイズム(誠実:公正・正直・不屈)」を根幹に、今後も、「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」というミッションの実現に向けて邁進してまいります。

その他の特色

■グローバルな事業運営をマネジメントできるビジネスリーダーを国内外で育成、獲得することに積極的な企業。海外のビジネススクールとも連携して、同社独自のエグゼクティブプログラムも開発されています。

※財務情報:国際会計基準の連結財務諸表より。売上高:売上収益、経常利益:税引前当期利益を記載。

売上実績

決算期
売上高
経常利益
2021/3
3,197,812百万円
366,235百万円
2022/3
3,569,006百万円
302,571百万円
2023/3
4,027,478百万円
375,090百万円
2024/3
4,263,762百万円
52,791百万円
2025/3
4,581,551百万円
175,084百万円

求人No.:NJB2375005

最終更新日:2026/4/16

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  3. 武田薬品工業株式会社:Manager, GDP Export Qualityの求人情報詳細