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R－99638 ＜品質保証部＞西神品質保証 Seishin QA/課長 Sr. Manager/M1/西神工場（神戸市内）
年収：応相談
採用企業案件
日本イーライリリー株式会社
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- 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
| 部署・役職名 | R－99638 ＜品質保証部＞西神品質保証 Seishin QA/課長 Sr. Manager/M1/西神工場（神戸市内） |
|---|---|
| 職種 | |
| 業種 | |
| 勤務地 | |
| 仕事内容 |
Main Purpose This position is responsible for ensuring the Site Quality System is followed and for ensuring quality products are manufactured and packaged at the site in compliance with applicable regulations such as Japanese GMP / QMS and global LQS / GQS. Some also are assigned to perform batch release to the market by Affiliate Quality. Responsibilities The Senior Manager is responsible for the following activities: General requirements Manage team members effectively and develop their capability Maintain “Well-Being” for team members according to “Red Book” and Lilly HSE policies, Ensure adequate number of qualified resources are available to perform required activities. Aid in human resource planning, development and performance management for direct reports Identify barriers to productivity within the unit operation and drive continuous improvement Mentor, coach and provide feedback to team members and cross-functional partners Support cross‑functional decision‑making and operational execution Develop and Execute Business & Strategy Planning Requirements related to Quality Department Make Quality and GMP decisions, including batch release decisions. Develop and maintain quality improvement projects. Ensure adherence to the quality policy and objectives for the site Drive Quality Culture improvement, including Data Integrity. Establish and maintain site Quality system for manufacturing operations to meet regulations including Japanese GMP, GQSs and LQSs. Establish and maintain site Quality system for marketed products which meet customer expectations. Maintain good relationship with Heath Care Authorities/Third parties/Oversea Sites /Lilly global Quality network. Collaborate with affiliate QA, other Lilly manufacturing sites, and global SMEs to solve quality issues. Participate in and ensure readiness for internal/external audit and inspection Business Title Sr. Manager, Quality Assurance |
| 応募資格 |
【必須（MUST）】 Educational background:Pharmaceutical Science, Chemistry, Biochemistry (bachelor degree or above) Work experience: Quality background with GMP and/or TS&MS knowledge and experience. Required language: Japanese and English 【歓迎（WANT）】 Personal ConsiderationKnowledge and Skills desirable to perform Role: ・Understanding the science of manufacturing. ・Understanding local and global applicable regulations. ・Modeling strong leadership behaviors. ・Having a global perspective. ・Capability to solve quality issues. ・Ability to influence diverse groups. ・Demonstrated decision-making and problem-solving skills ・Ability to work as part of a team ・Demonstrated negotiating coaching and mentoring skills ・Experience leading teams |
| 受動喫煙対策 | 屋内禁煙 |
| 更新日 | 2026/02/10 |
| 求人番号 | 7285955 |
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。
転職・求人情報の詳細をご覧になる場合は会員登録（無料）が必要です