Make your mark for patients
患者さんのためにあなたの力を発揮してください
私たちは、情熱を持ち、前向きで、責任感の強いサプライチェーンマネージャーを募集しています。
埼玉 の製造拠点にあるサプライチェーンチームの一員として活躍し、安定供給と高品質な製品づくりを支える重要な役割を担っていただきます。
【チームについて】
本ポジションを募集しているチームでは、生産管理、調達、在庫、倉庫、物流まで一連のサプライチェーン業務を担当しています。
チームはグローバルの関係者と協力しながら、安定供給と品質確保を両立させることを使命としています。
部門内外との連携が多く、常に改善を重ねながら事業を支えるプロフェッショナル集団です。
【主な業務内容】
・生産計画、在庫、調達、倉庫、配送プロセスの管理
・主要指標を用いたサプライチェーン全体の運営改善
・業務システムを活用した効率的な運用の推進
・社内外との連携による需給調整への貢献
・サプライヤーの評価、協働、管理
・品質基準に基づく倉庫環境の維持と改善
【必要な経験スキル】
・学士号以上の学歴
・製造工場での生産計画の立案経験
・生産計画に関する業務システム(SAP)利用経験
・英語力:Low Business Level 以上
【あれば尚可】
・製薬業界でのサプライチェーン経験 5 年以上
・直接購買での調達の経験
【求める人物像】
・部門横断の中規模プロジェクトリーダー経験
・品質基準を理解し文書作成および改善ができる方
・多様な関係者と協力できるコミュニケーションスキル
【応募方法】
・日本語の履歴書と職務経歴書を 1 つのファイルにまとめ、応募時にアップロードしてください
・UCB 社員からの紹介がある場合は、応募時にその旨をご記載ください
(English Follow)
Job Summary
Stable supply and Production of stable quality products with Competitive cost through Qualified system and Procedure by Motivated person.
Major Accountabilities/Responsibilities
Lead production control, inventory control, purchasing, warehouse management and delivery.
Control the related KPIs for SCM (OTIF, Plan Attainment, Release Adherence, Late MRP, Inventory, Turns, discards, Warehouse capacity, etc)
Fully apply and expand SAP knowledge (MM, PP, WH, QM, SD) to operate in the most efficient way
Represent from Site Supply Chain to contribute to the efficient S&OP in the company.
Implement, Collaborate, Evaluate, Manage Suppliers including CMOs/Carriers.
Keep/Improve a condition/environment in warehouse from the viewpoint of GMP requirements.
Create, maintain and update the SOPs to keep and develop the knowledge within the team
Lead the cost saving projects.
Lead the change management related to Supply Chain.
Control good-conditioned utilities and equipment in warehouse.
Set a short and long-term target linked to plant goal.
Proactive approach to develop and keep good relationship with stakeholders (within Plant, UCB Tokyo/Global, suppliers, partners, etc)
Report to Head of Saitama Supply Chain
Education & Qualifications
Education Level : Bachelor's Degree
Experience : Experience in Supply Chain Management in Pharmaceutical industry: over 5 years in production site.
SAP Experience: over 5 years in production planning. (S/4 Hana preferred)
Experience as project leaders with middle magnitude for the company: at least 1 project
Competencies
Ability to lead mid-sized projects involving cross-departmental collaboration.
Acquired knowledge of HSE and 5S principles, and ability to apply them effectively to operations.
Strong understanding of systems and processes, with the ability to utilize and manage them optimally.
Deep understanding of operational processes and the ability to lead improvement initiatives.
Ability to identify and resolve issues effectively.
Ability to operate with a deep understanding of and adherence to GMP standards.
Ability to comprehend international regulations such as PIC/S and ICH, and apply them effectively to operations.
Ability to propose and implement improvements to the team's quality system.
Ability to systematically prepare GMP-compliant documents with appropriate content, and to review and verify GMP-related materials.
Ability to instruct and educate both within one's own division and across other divisions on relevant GMP practices.
Possesses strong communication skills to build positive relationships with stakeholders and team members, and to report, consult, and collaborate effectively for smooth operations.
Demonstrates mutual respect by actively seeking, sincerely considering, and integrating others' opinions through constructive discussion; fosters a respectful team culture.
Capable of leading the development and execution of strategies for problem-solving, root cause analysis, and recurrence prevention for major issues within the department, as well as cross-functional challenges.
Able to collect diverse information and make optimal decisions while managing appropriate risks within the scope of assigned responsibilities.
Contributes to team-based decision-making, takes ownership of implementation, and clearly communicates decisions within the department to ensure effective execution.
Understands and is able to implement the PVS Principles.
Capable of explaining the PVS Principles to team members and encouraging their adoption.
Demonstrates a strong passion for personal growth and the ability to learn in a structured and systematic manner.
Inspires and motivates team members to achieve shared goals and continuous improvement.
Complies with laws, regulations, company policies, workplace rules, and professional etiquette, and ensures team members also adhere to these standards.
Manages personal health and well-being to fulfill assigned duties effectively; proactively supports the health of team members and takes initiative in fostering a healthy work environment.
Demonstrates strong communication skills within the factory, across related departments, and globally; able to collaborate effectively with external suppliers to resolve complex issues.
Understands the strategic objectives of the Saitama Plant and aligns departmental and personal goals accordingly.
Demonstrates a clear understanding of the Saitama Plant's structure and operations, with the ability to confidently explain them to visitors; possesses in-depth knowledge of own department and its functions
Able to communicate professionally in English via email; capable of reading and understanding GMP and other technical documents in English.
Understands basic accounting systems and terminology.
患者さんのために価値を創造し、ご自身の力を発揮する準備ができているお感じでしたら、ぜひ私たちにご連絡ください。
会社概要
UCBは、神経および免疫領域に注力するグローバルなバイオ医薬品企業です。世界中で約8,500人の社員が、患者さんからインスピレーションを受け、科学の力で前進しています。
UCBで働く魅力
UCBでは、単に業務をこなすのではなく、価値を創造することを大切にしています。私たちは挑戦を恐れず、協力し合い、革新を追求しながら、患者さんのために成果を出すことを目指しています。
誰もが尊重され、受け入れられ、最善を尽くせる平等な機会がある、思いやりと支援に満ちた文化が根付いています。
私たちは常に「その先」を目指し、患者さん、社員、そして地球に対して人間らしさを大切にした価値を提供しています。
UCBで働くことで、自分自身の成長を実感し、自由にキャリアを築き、可能性を最大限に引き出すことができます。
UCBでは機会均等を重視しています。すべての採用決定は、法律で保護されているいかなる属性にも関係なく行われます。
選考プロセスにおいて、ご自身の強みや能力を十分に発揮できるよう配慮が必要な場合は、以下のメールアドレスまでご連絡ください:
EMEA-
※なお、この問い合わせ先では選考における特別な配慮に関するご相談以外はお受けできませんので、ご注意ください。
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