非公開施設の管理者・施設長 (正社員) の求人・転職・就職募集情報

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この求人の掲載元:製薬オンライン

  • 募集内容

  • 事業所情報

募集職種

管理者・施設長  

雇用形態

正社員

仕事内容

As a key partner to the business, the Head of External Manufacturing and Sourcing (EM&S) is responsible for the strategic planning and execution of EM&S operations across three of company's Regions (Japan, China and Asia). This position leads and manages the manufacturing, sourcing and Contract Manufacturing Organisations (CMOs) for all company products produced externally within the Region. Additionally responsible for assessing new business development opportunities and for developing and implementing the required organization, standards, processes and procedures. The position reports to the Head of Global EM&S and is responsible for delivering overall performance results from the Regions’ CMO network. - Drives and develops the regional EM&S vision in partnership with global EM&S, for pharmaceutical and biologics CMOs - Develops the strategy for EM&S across the Region, with direct accountability for external manufacturing operational performance, including on-time in-full supply, COGS management, capacity management and business continuity planning. - A key member of the Product Supply (PS) department, provides strategic input and ensures alignment with senior stakeholders to ensure the attainment of the company’s short- and long-term goals. - Implements and leads Supplier Relationship Teams (SRTs) to manage the key strategic partners, acting as the virtual plant manager for the CMO, with matrix responsibility for cross-functional team members such as Quality, Planning, Procurement, Project Management and MS&T. Ensures optimal supplier relationship management and the seamless delivery of products to meet the needs of the business. - Negotiates and runs RFPs to ensure the continuity of product supply requirements and delivers timely execution of Technical Transfer projects, for existing and new product launches. - Leads external manufacturing and sourcing in a cost-efficient manner, developing quantitative performance monitoring and the rollout of relevant KPI’s that can be used as a platform to continuously improve supply from external manufacturers. - Builds a quality ethos into all decisions and processes, reinforcing the implementation of company's Global Tech Transfer Process (GTTP) standards to support Make-or-Buy decisions, Supplier Selection, Technology Transfers and the Management of Commercial Products. - Owns and controls the regional EM&S budget including capital investments with external partners, technical transfer expenses and other expenses needed to support the life cycle management of the products. - Drives change management and continuous improvement of EM&S, driving end-to-end value creation projects across the total supply chain to deliver competitive advantage for the business. - Provides due diligence evaluation and advice on new sourcing and external manufacturing business opportunities in partnership with the Business Development (BD) team. Manages the integration and set up of new BD suppliers and represents company on external governance committees, such as Joint Manufacturing Committees. - Negotiates and executes legal contracts, together with the Legal and BD teams, including Manufacturing & Supply Agreements and Technical Transfer Agreements, structuring such contracts in an optimal manner to ensure the security of long-term supply and the protection of the company business - Performs other duties as necessary as assigned by management

給与

正社員:年収 12,000,000円〜17,000,000円

給与の備考

年収  1200万円~1700万円

待遇・福利厚生

通勤手当:有 寮・社宅:有 住宅手当:有

試用期間

3ヶ月

勤務時間

フレックスタイム制 フルフレックス(コアタイムなし)

休日

年間休日数:123 土日祝 年間有給休暇:下限日数は、入社直後の付与日数となります 10日 ~ 20日 法定休暇:年次有給休暇 特別休暇:夏季休暇、年末年始休暇

応募要件

Degree in Life Sciences, Biological Sciences or Product Supply related areas. - Ten years plus experience in product supply and manufacturing in the pharmaceutical industry and/or the biologics industry - Experience and solid track record in leading and managing external manufacturing suppliers in Asia - Solid understanding of the drug development process, of GMP requirements and the manufacturing of sterile products. Cell and gene therapy awareness an advantage - Strong understanding of end-to-end supply chain management requirements - Experience in a matrix organization, operating and communicating with senior level management, both internally and externally, and managing interdepartmental processes. - Strong business acumen, and demonstrated improvements of business performance (optimization of cost, resources, results), as well as a sound understanding of relevant financial and legal aspects - Experience in leading and managing in an international environment.

最終更新日:2026/4/14

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