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Associate Director, Lead Of Capital Projects, Engineering (CAPEX)

年収:1200万 ~ 1400万

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部署・役職名 Associate Director, Lead Of Capital Projects, Engineering (CAPEX)
職種
業種
勤務地
仕事内容 OBJECTIVES/PURPOSE

- Guarantee GMP and implement pharmaceutical engineering.
- Manage project efficiently and analyze / challenge total costs.
- Respect environment and ensure people and assets safety.
- Develop manufacturing knowledge and transfer the technological expertise.
- Challenge business needs and develop the optimum solution.
- Manage suppliers’ relationship.

ACCOUNTABILITIES

- The Capital Projects Engineering Manager is a subject matter expert (SME) with respect to all Capital portfolio management and project delivery activities. In this role, he / she is responsible for capital program and project activities within the Site Engineering function.
- The Capital Projects Manager is an integral member of the Site Engineering Leadership Team who interacts closely with the Operational Managers within the Site to ensure all capital projects are delivered to support reliable and robust manufacturing operations.
- The Capital Projects Manager ensures that the Capital Projects team is staffed with the appropriate skills and capabilities to meet all Site Engineering functional goals. He / she establishes an efficient capital delivery organization focusing on right first time delivery and following industry best practices to meet the strategic needs of the Hikari Manufacturing Plant.
- The Capital Projects Manager ensures that all capital projects result in fit for purpose assets which meet the business requirements (safety, functionality, capacity, capability, maintainability, compliance and reliability) in a timely and cost effective manner.
- The Capital Projects Manager ensures that adequate technical and numerical support is provided to the capital projects team to assure the success of all capital projects under his / her control.
- Plan and control engineering capital expenditures for the site with ensuring compliance to Corporate, and Site financial policies.
- Ensure GMP compliance and conformance to all regulatory requirements, establish and maintain standards for equipment validation along with the quality department. Execute a validation strategy that identifies all critical inputs and controls them properly to achieve optimal performance of critical process/product outputs.
- Lead and manage IOQ and calibration activities
- Run CAR application process for all CAPEX projects and review all the project charter in advance.
- Ensure effective training and development of Department personnel.
- Set goals for long range planning and plant profit performance improvement.
労働条件 正社員

諸手当:通勤交通費、借家補助費、勤務時間外手当など
昇給:原則年1回 
賞与: 原則年2回
勤務時間:工場(山口県光市)8:00~16:45
休日:土曜、日曜、祝日、メーデー、年末年始など(年間123日程度)
働き方関連制度:フレックスタイム制、テレワーク勤務制導入(対象社員)
休暇:年次有給休暇、特別有給休暇、傷病休暇、ファミリーサポート休暇、産前産後休暇、育児休暇、子の看護休暇、介護休暇
応募資格

【必須(MUST)】

EDUCATION, BEHAVIOURAL COMPETENCIES AND SKILLS

Degree in engineering (Dipl. Ing. / M. Sc. / B. Sc.) or equivalent (mechanical / process / chemical or equivalent
Languages: Fluent business level English capability. Fluent Japanese writing and verbal communication skills required.

Experience:

At least 10 years in Projects Management, including 5+ years as Project.
Manager of sizeable investment projects; exposure to GMP or other highly regulated projects is required, preferably in the pharmaceutical industry.
High communication skills, analytical mind-set, ability to work under pressure.
GxP/QA knowledge.
Innovative thinking.
Building relationships and teamwork.
Can establish and coordinate service contracts with engineering service providers.

【歓迎(WANT)】

PMO certification
Experience in Manufacturing or operations.
Experience of working in overseas countries.
Know how in qualification and validation processes is a plus.

アピールポイント 自社サービス・製品あり 日系グローバル企業 女性管理職実績あり 上場企業 従業員数1000人以上 創立30年以上 年間休日120日以上 産休・育休取得実績あり ストックオプション制度あり 教育・研修制度充実 資格支援制度充実
更新日 2020/10/12
求人番号 1518250

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