生産技術・製造技術・エンジニアリング(メディカル)
Head of Production Engineering Group
掲載期間:24/10/29~24/12/23求人No:RES-34266228
生産技術・製造技術・エンジニアリング(メディカル)

Head of Production Engineering Group

外資系企業 上場企業 英語力が必要 土日祝休み

募集要項

募集背景
Production Engineering Group Lead reports to Head of Saitama Site. This role leads and manages the group to provide technical services for the projects and engineering tasks, related to dosage form production and Packaging. She/he is responsible to realize Saitama site strategy as a member of site leadership team. She/he is also responsible to grow Saitama members.
仕事内容
Major Accountabilities/Responsibilities

• Rollout the strategy, goals of Saitama site and Technical Service department into the group strategy and targets. Lead and manage the group to achieve the targets and realize the strategy.
• Responsible for the Saitama site strategy and KPIs comprehensively across the functions
• Control and manage the resource and capability to deliver the projects, related to the production engineering.
• Control and manage the OPEX, CAPEX and Head Count budget to meet the goal.
• Responsible to contribute for saving target.
• Lead and/or manage Dosage Form & Packaging projects.
• Responsible for the group to achieve following responsibilities.
- Mange and lead Dosage Form & Packaging projects and technical transfer of new products.
- Manage and lead the engineering work for Dosage Form & Packaging lines.
- Manage and lead the maintenance, calibration, and renewal work for Dosage Form & Packaging lines.
- Manage and lead repairment work for Dosage Form & Packaging lines.
- Manage and lead GxP and relevant raw execution for the Dosage Form & Packaging related matters.
- Manage and lead to Improve the Dosage Form & Packaging processes and equipment for a better efficiency and HSE.
- Manage and lead the packaging material development and design.
- Manage and lead artwork development.
• Grow next technical leaders and grow the group in leadership and technical skills.
• Build connection in UCB widely in both local and global for stakeholder management.
• Build good relationship with the suppliers in the market widely and manage and control them.
Update the technical capability of the group according to the progress in technology.
応募資格
必須
Qualifications
・Experience in process development or production line engineering of pharma industry for 5 years or more
・Team leading experience, preferably people management experience
歓迎
Competencies
1. Process Development:
● Deep and wider understanding of manufacturing processes and technologies of pharma industry.
● Deep and wider understanding of manufacturing equipment, include maintenance and troubleshooting.
● Deep and wider understanding of raw materials, packaging materials in chemical, physical properties, and the production process.
● Deep and wider understanding of validation for process developments and/or production line installation.
● Deep and wider understanding of analytical methods and analytical method transfer process.
● Basic business level understanding of packaging development, planning and scheduling the day-to-day operations of the manufacturing department.
● Basic business level understanding of End-to-End Supply Chain process about the products.
● Understanding industry-wide trends and having insights into the strategic direction of the organization.
2.Quality System and Regulation Management:
● Deep and wider understanding about GxPs, relevant regulations and guidelines regarding Production, Process, Analytical and Packaging development. And the execution skills of the Quality System.
● Basic Business Level knowledge about the entire GxPs and other relevant regulations related to pharmaceutical industry.
● Skills in ensuring and maintaining product and execution quality through effective quality management.
3.Sustainability and Efficiency
● Skills to considering sustainability and efficiency across the entire manufacturing process and development process from a broader perspective.
雇用形態
Full Time
勤務地
Saitama Prefecture
年収・給与
13 million yen ~ 15.99 million yen

会社概要

社名
非公開
事業内容・会社の特長
神経学と免疫学に特化したグローバルなバイオ医薬品企業です。世界各地に約8,500人の従業員を擁し、患者さんに触発され、科学を原動力としています。

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SThree株式会社
厚生労働大臣許可番号:13-ユ-305733紹介事業許可年:平成25年
設立
2012年(日本オフィスの立ち上げ)
資本金
3億980万円
代表者名
Chris Reilly
従業員数
法人全体:120名

人紹部門:90名
事業内容
STEM領域(Science, Technology, Engineering, Mathematics)に特化したロンドン証券取引所上場の人材紹介業で、日本オフィスでは5ブランドのチームに分かれており、それぞれ下記の通り、細かく担当領域を分けて特化しています。

• Computer Futures: IT、テクノロジーの企業と職種
• Progressive Recruitment: 再生可能エネルギー、エンジニアリング、自動車、ロボットメーカーなどの企業と職種
• Real Life Sciences: 医療機器、製薬、ヘルスケアの企業と職種
• Huxley: 金融サービス、プロフェッショナルサービス(リーガル、コンプライアンス、アカウンティングなど)の企業と職種
• Global Enterprise Partners: SAP, ERPの使用企業と職種(業務委託・派遣)
厚生労働大臣許可番号
13-ユ-305733
紹介事業許可年
平成25年
紹介事業事業所
東京、ブリズベン、シドニー、ベルギー、ブリュッセル、パリ、フランクフルト、オランダ、アムステルダム、シンガポール、チューリッヒ、バーミンガム、リーズ、ロンドン・シティ、ロンドン・ソーホー 、ボストン、シカゴ、ニューヨーク、サンディエゴ 、サンフランシスコ
登録場所
SThree株式会社
〒104-0061 東京都中央区銀座4-12-15歌舞伎座タワー9階
ホームページ
https://www.sthree.com/
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