Sommario
About the Role
Key Responsibilities:
- Build and maintain strong relationships with internal and external Novartis stakeholders, particularly strong working relationships to ensure effective and seamless collaboration with the Operations Centre and Site Development.
- Set up, troubleshoot, and maintain the entire packaging floor in all formats within the timeframe required to meet departmental expectations and efficiencies.
- Improve the effectiveness of operations by researching process methods, making recommendations for improvements, and assisting in the implementation of such improvements.
- Maintain FDA-compliant operations with appropriate documentation.
- Support engineering studies, validation, FAT and qualification and provide input to equipment-related SOPs.
- Maintain compliance with SOPs, Good Documentation Practice (GDP), training requirements, company and safety policies (e.g. lockout/tagout) and current good manufacturing practice (cGMP).
- Support other lines and roles as required to maintain operational efficiency and production output without compromising quality or safety.
- Comply with all applicable procedures, cGMPs, company policies and all other quality or regulatory requirements (e.g. OSHA, DEA, FDA, EMEA, ANVISA, HS&E).
- Ensure that all work is performed in a safe and effective manner and in compliance with appropriate industry and regulatory (FDA, DEA, OSHA) standards, as well as departmental, plant and corporate quality and safety behaviors
- Training of machinery and packaging personnel
Requirements:
- No academic qualifications required.
- English language skills at business level and the ability to communicate fluently in Japanese.
- Experience in engineering project management.
- Experience in production and manufacturing engineering and the ability to design to EHS standards
主な役割責任
- ノバルティス社内外のステークホルダーと強い関係を築き、維持し、特にオペレーションセンターやサイトディベロップメントと効果的かつシームレスに連携するための強力な協力関係を構築する。
- 部門の期待と効率を満たすために必要な時間枠内で、あらゆるフォーマットのパッケージングフロア全体のセットアップ、トラブルシューティング、メンテナンスを行う。
- プロセス方法を研究し、改善のための提案を行い、そのような改善の実行を支援することにより、業務の有効性を向上させる。
- FDAに準拠したオペレーションを維持するため、適切な文書化を行う。
- エンジニアリングスタディ、バリデーション、FAT、資格認定を支援し、装置関連のSOPにインプットを提供する。
- SOP、Good Documentation Practice (GDP)、トレーニング要件、会社および安全方針(ロックアウト/タグアウトなど)、および現行の適正製造基準(cGMP)の遵守を維持する。
- 品質や安全性を犠牲にすることなく、業務効率や生産量を維持するために、必要に応じて他のラインや役割をサポートする。
- 適用されるすべての手順、cGMP、会社方針、その他すべての品質または規制要件(OSHA、DEA、FDA、EMEA、ANVISA、HS&Eなど)を遵守する。
- すべての作業が、安全かつ効果的な方法で、適切な業界および規制(FDA、DEA、OSHA)基準ならびに部門、工場の品質および安全に関する行動を遵守して行われていることを確認する。
- 機械および包装担当者のトレーニング
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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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