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福島県の求人617件応募資格・募集要項・仕事内容を見る
GMP Coordinator
- 給与
- 記載なし
- 勤務地
- 福島県
- 休日
- 記載なし
- 雇用形態
- 記載なし
どんな仕事かAIによる生成
As a GMP Coordinator at Koriyama Factory, you will ensure GMP compliance across the site and connect local production operations with global quality standards. The role coordinates across production, engineering, QA, and QC, supports regulatory inspections and audits, and helps implement global requirements as local procedures.
この求人に応募
応募資格
必須
- Strong understanding of GMP regulations and their practical application in a manufacturing environment
- Business-level English (required) for daily communication with global colleagues and stakeholders
- Excellent communication and coordination skills, with the ability to work across functions and build relationships at all levels
歓迎
- Preferably 3+ years of experience in Production, Engineering, QA, or QC within the pharmaceutical industry; experience from medical device, food, or cosmetics industries is also relevant, provided you have solid GMP knowledge
- Preferably fluent Japanese to collaborate effectively with local teams
募集要項最終確認 10/20
- 職種
- 品質管理
- 雇用形態
- 記載なし
- 給与
- 記載なし
- 勤務地
- 福島県Koriyama
- 働き方
- 記載なし
- 掲載日
- 2026/10/12 05:36（9日前）
- 最終確認
- 2026/10/20 15:28（1日前）
仕事内容
募集内容
- Bridge local manufacturing excellence with global standards – and help ensure life-saving medicines reach patients across the world from our Koriyama Factory.
Your new role
- As a GMP Coordinator at Koriyama Factory, you will be the key link between local production operations and global quality standards, ensuring GMP compliance across the site. Reporting directly to the Head of Production, you will drive cross-functional collaboration and maintain close communication with global stakeholders to uphold the highest manufacturing standards.
- Your key responsibilities will include:
- Coordinating and maintaining GMP compliance across production, engineering, QA, and QC functions at the Koriyama Factory
- Serving as the primary point of contact for global GMP-related communication, aligning local practices with Novo Nordisk’s global standards
- Facilitating wide cross-functional interactions between departments to ensure consistent quality and compliance
- Supporting preparation for and follow-up on inspections and audits from regulatory authorities
- Driving continuous improvement initiatives related to GMP processes and documentation
- Translating global requirements into actionable local procedures and ensuring their implementation
Your new department
- At Koriyama Factory, we are proud to be part of this global manufacturing network. Our team works with dedication and precision to deliver high-quality pharmaceutical products, collaborating closely with colleagues both locally and internationally. You will join a site where teamwork, accountability, and a direct connection to patients define how we work every day.
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応募はノボ ノルディスク ファーマ株式会社の採用ページで受け付けています。このページは採用ページの掲載内容をもとに構成しているため、最新の応募条件は募集元でご確認ください。