Zusammenfassung
About the Role
Major accountabilities:
- 製造工程内で生産する全てのプロセス固有の問題に対して最前線の専門サポートを提供すること。
- 品質と生産性を継続的に改善すること。
- cGMP、SOPs、適用可能なガイドラインと規範に従って行動すること。
- 日本の法的要件のみならず、Novartisが求めるGMP/HSE スタンダードを関係部署と協働しながらプロセスユニット部全従業員へ展開することにより、高品質製品の安定供給と業績目標達成に貢献すること。
必須要件:
- 学歴は不問
- 医薬品製造プロセス、製造機器に関する知識
- 製造業の製造現場で3年以上の業務経験(分野は問わない)
- 科学的に物事を考える事が出来る人。
- 幅広い世代とのコミュニケーションがとれる人。
- 日本語が流暢であること。英語にアレルギーがないこと。
望ましい要件:
- 薬機法、GMP等の規制に関する知識
- チームをリードした経験
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
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Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
Accessibility and accommodation
Novartis is committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
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