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| 部署・役職名 | R-97330 Site Master Planning and Project Engineer |
|---|---|
| 職種 | |
| 業種 | |
| 勤務地 | |
| 仕事内容 |
Site Master Planning and Project EngineerCompany: Eli Lilly Japan K.K. Location: Seishin Laboratories (西神工場) At Lilly, we believe in the talent of our workforce. One of the best ways to utilize and develop that talent is to use our existing workforce to fill new and/or open positions. If you are looking for a new position within Lilly, you can view and apply to open roles posted in the internal job posting system. You must meet the minimum qualifications outlined in the job description and have/obtain work authorization in the country the position is located in order to be considered. When applying internally for a position, your current supervisor will receive notification that you have applied to the position. We encourage employees to discuss the opportunity with their supervisor prior to applying. ---Path/Level: P1-P3 Note: Roles are posted at the lowest level of a band, however, employees should search across all levels of the band to identify all opportunities. Employees hired on banded positions (ex: P1-P3, R-path, B1-B3, etc.) transfer at their current level, despite the level indicated on the job posting. For example, if a P2 candidate is selected for a P1-P3 banded position, the candidate will remain a P2 in the new role. ---Job Summary The Site Master Planning and Project Engineer will be responsible for developing and implementing strategic site master plans and executing capital projects to support Eli Lilly Japan K.K.'s manufacturing and operational growth, ensuring alignment with global standards and local regulations. ---Job Responsibilities * Strategic Planning: Develop, maintain, and update the long-range site master plan, incorporating business growth forecasts, technological advancements, operational efficiency improvements and facility fit-and-finish. * Project Management: Lead and manage capital projects from conception to completion, including scope definition, budget development, schedule management, resource allocation, and risk mitigation. * Engineering Design & Execution: Oversee and contribute to the engineering design, procurement, construction, and commissioning phases of various projects, ensuring adherence to safety, quality, and environmental standards. * Stakeholder Collaboration: Collaborate effectively with internal stakeholders (e.g., manufacturing, quality, regulatory, HSE, finance) and external partners (e.g., contractors, vendors, consultants) to ensure project success and alignment with company objectives. * Regulatory Compliance: Ensure all project activities and site master plans comply with relevant Japanese regulations, Good Manufacturing Practices (GMP), and Eli Lilly global engineering standards. * Cost Control & Optimization: Manage project budgets, track expenditures, and identify opportunities for cost savings and process optimization without compromising quality or schedule. * Technical Expertise: Provide technical expertise and guidance on facility design, utility systems, process equipment, and infrastructure development. * Continuous Improvement: Identify and implement best practices in project management, engineering, and site planning to drive continuous improvement within the organization. ---Job Qualifications * Education: Bachelor's degree in Engineering (e.g., Chemical, Mechanical, Civil, Industrial) or a related technical field. A Master's degree is a plus. * Experience: Minimum of 7-10 years of experience in site master planning, capital project management, and engineering roles within the pharmaceutical, biotechnology, or a highly regulated manufacturing industry. |
| 応募資格 |
【必須(MUST)】 ---Technical Skills:*Proven experience in leading complex engineering projects from initiation to close-out. *Strong understanding of GMP, HSE regulations, and quality systems. *Experience with facility design, utility systems, and process equipment. ---Soft Skills: *Excellent leadership, communication, and interpersonal skills with the ability to influence and collaborate across various functions and levels. *Strong analytical and problem-solving abilities. *Demonstrated ability to manage multiple projects simultaneously and prioritize effectively in a fast-paced environment. *Fluency in Japanese (written and spoken) is essential, and strong English communication skills (written and spoken) are required for interaction with global teams. * Attributes: Proactive, detail-oriented, results-driven, and committed to continuous learning and improvement. 【歓迎(WANT)】 Master's degree |
| 受動喫煙対策 | 屋内禁煙 |
| 更新日 | 2026/01/16 |
| 求人番号 | 6550097 |
採用企業情報
- 日本イーライリリー株式会社
-
- 資本金12,772百万円
- 会社規模501-5000人
- 医薬品メーカー
- その他
- CRO
-
会社概要
【設立年月日】1975年11月1日
【代表者】シモーネ・トムセン
【資本金】127億7,250万円
【売上高】2,167億円(2022年度)
【従業員数】約2,700名(2022年末現在)
【本社所在地】兵庫県神戸市中央区磯上通5-1-28 LILLY PLAZA ONE BLDG.
【その他事業所】
事業所:神戸(本社)、東京支社
工 場・研究所:神戸
【事業内容】医療用医薬品の製造および販売
【当社について】
1876年に創業、130年を超える歴史があるイーライリリー・アンド・カンパニー。
米国インディアナ州インディアナポリスに本社を置く、革新を追求する医薬品のリーディング・カンパニーです。
世界各国の自社研究施設や外部の優れた科学的研究機関との提携による新しい研究成果を用いて、各治療領域で最高レベルの豊富なポートフォリオの医薬品を開発しています。世界125カ国以上で事業を展開しています。
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