Tokyo,8.0M ～ 10.0M

-Manage procurement activities for specific categories of raw materials used internally, such as dairy ingredients, processed fruits, and additives.
-Analyze and forecast internal business needs, raw material markets, and environmental impacts to develop mid-term strategies for assigned categories.
-Based on the agreed category strategy, develop accurate and realistic implementation plans. Execute these plans without delay in collaboration with internal departments and external stakeholders. This includes identifying new suppliers and packaging materials, building relationships with strategic suppliers and key stakeholders, negotiating contract terms, and conducting tenders.
-Ensure proper internal controls, including contract management and promotion of Danone’s global supplier audit system.
-Lead cross-functional cost reduction and value creation projects.
-Regularly report on raw material costs, value, and progress of cost-saving initiatives through global and Japan scorecards.

Tokyo,7.0M ～ 12.0M

デバイスやチャネルにあったユーザー体験の設計を主とし、業務ユーザーやエンジニアと連携しながら、アジャイル開発手法やリーン思考を活用したユーザーエクスペリエンスの実現を行うことを期待しています。具体的には以下です。
・当グループの社員や店舗スタッフが日々の業務で使うツールやシステムのUX・UIデザイン ・ユーザーニーズに基づいたUX戦略、コンセプトの開発 ・情報設計、サイトマップ、ワークフロー、ワイヤーフレーム、プロトタイプの作成 ・UX Researcher と連携しユーザー調査の実施、ユーザビリティの検証
・業務の理解や課題抽出のためのヒアリング、および現場での仮説検証
・社内向けデザインガイドラインの更新・運用 ・ユーザーニーズに基づいたより革新的なユーザーエクスペリエンスを提供する為の設計や手法の開発 組織を横断した幅広い協業が期待されます。また、ビジュアルデザインの専門性、情報設計力、ユーザー視点のインタラクションデザイン能力などを活かして頂きます。

Tokyo,12.0M ～ 16.0M

Your role:
Exciting opportunity to lead the team working on Cardiac and Endovascular registration projects for Image-guided Therapy, which includes novel technologies integrated by therapeutic devices and visualization systems.

- Lead the Japan Senior Manager and all clinical studies and evidence development projects that the team is responsible for to proceed with the plan.
- Lead developing local clinical evidence development strategy and strategic discussion with the local RA team and other related stakeholders, including - - - - Business Unit, R&D, and Market Access & Reimbursement to accelerate projects and fast serve patients.
- Proactively identify risks within clinical evaluation strategies, plans, products and propose alternate approaches.
- Provide interpretation of local regulations to BU partners and ensure necessary requirements are fully deployed.
- Stay informed of new regulations and technologies relevant to endovascular therapeutics.
- Plan and execute clinical evidence development, GCP compliance review of foreign operated clinical trials, and PMS study as a condition of approval according to the regulations and aligned with local business needs.
- Manage interactions with MHLW/PMDA/KTLs and maintain a productive working relationship.
- Manage CRO services to ensure meeting with business needs and operational policies.
- Review and approve clinical documentation according to the GCP/GPSP requirements.
- Oversee clinical administration activities.
- Report to the Head of Japan as a solid line