Compliance & Quality System Manager

**Summary**: - Manage cost effective GxP Compliance and/or Audit activities, operations and systems to ensure compliance of business areas with the Novartis Quality Manual and Policies and all relevant GxP, legal and regulatory requirements, and through internal audits, KPIs (Key Performance Indicators) and KQIs (Key Quality Indicators) -Lead the...

**Summary**: ~Verwalten Sie kostengünstige GxP-Compliance - und/oder Audit-Aktivitäten, -Abläufe und -Systeme, um die Einhaltung des Qualitätshandbuchs und der Richtlinien von Novartis sowie aller relevanten GxP-, gesetzlichen und regulatorischen Anforderungen sowie durch interne Audits, KPIs (Key Performance Indicators) und KQIs (Key Quality Indicators)...

**Summary**: ~Beheer kosteneffectieve GxP Compliance - en/of Audit-activiteiten, -activiteiten en -systemen om ervoor te zorgen dat bedrijfsonderdelen voldoen aan de Novartis Quality Manual and Policies en alle relevante GxP-, wet - en regelgevingsvereisten, en door middel van interne audits, KPI's (Key Performance Indicators) en KQIs (Key Quality...

**Summary**: ~Gérer les activités, opérations et systèmes rentables de conformité GxP et/ou d’audit pour assurer la conformité des secteurs d’activité avec le manuel et les politiques de qualité de Novartis et toutes les exigences GxP, légales et réglementaires pertinentes, et par le biais d’audits internes, d’indicateurs clés de...

**Summary**: ~İş alanlarının Novartis Kalite El Kitabı ve Politikaları ile ilgili tüm GxP, yasal ve düzenleyici gerekliliklere uygunluğunu sağlamak için ve iç denetimler, KPI'lar (Anahtar Performans Göstergeleri) ve KQI'ler (Anahtar Kalite Göstergeleri) yoluyla uygun maliyetli GxP Uyumluluğu ve/veya Denetim faaliyetlerini, operasyonlarını ve...

**Summary**: ~ Gestionar las actividades, operaciones y sistemas rentables de cumplimiento y/o auditoría de GxP para garantizar el cumplimiento de las áreas de negocio con el Manual y las Políticas de Calidad de Novartis y todos los requisitos relevantes de GxP, legales y reglamentarios, y a través de auditorías internas, KPI (Indicadores clave de...

**Summary**: ~費用対効果の高いGxPコンプライアンスおよび/または監査活動、運用、およびシステムを管理し、ノバルティス品質マニュアルおよびポリシー、および関連するすべてのGxP、法的および規制要件、および内部監査、KPI(主要業績評価指標)、KQI(主要品質指標)を�...

**Summary**: ~管理具有成本效益的 GxP 合规性和/或审核活动、运营和系统，以确保业务领域符合诺华质量手册和政策以及所有相关的 GxP、法律和法规要求，并通过内部审核、KPI（关键绩效指标）和...

**Summary**: TRD Quality Process & Engineering Manager will collaborate with RLT Engineering organization for RLT TRD, to establish, maintain and improve the engineering processes with respect to buildings, equipment, utilities and energy. This role includes oversight of operational and validation activities and continuous process improvements. **About the...

CBS Lavoro S.p.a. Filiale di Santhià ricerca **QUALITY MANAGER **per azienda operante nel settore **progettazione e realizzazione di componentistica pneumatica**. **La risorsa si occuperà di**: - **Revisionare e redigere il piano qualità aziendali - Analisi delle esigenze del cliente - Definizione del livello standard di un prodotto e di un processo -...

SummaryTo lead the Ivrea TRD RLT Pilot plant Quality Control (QC) team by developing and executing strategic plans, providing direction for organizational structure, GMP and safety strategy, lean and continuous improvement initiatives, and people training and development. The QC Head is responsible for ensuring that the lab unit meets all agreed-upon...

On behalf of a Multinational Pharmaceutical company, Gi Group LifeScience Division is looking for 2 Quality Control Technician Our client is an innovative medicines company focused on the development of products for targeted radioligand therapy and precision radioligand imaging. **Major Accountabilities**: Perform the analysis of batches following...

To lead the Ivrea TRD RLT Pilot plant Quality Control (QC) team by developing and executing strategic plans, providing direction for organizational structure, GMP and safety strategy, lean and continuous improvement initiatives, and people training and development. The QC Head is responsible for ensuring that the lab unit meets all agreed-upon objectives and...

Global Quality Platform Head RLT (remote)SummaryAt Advanced Accelerator Applications, a Novartis Company, we are committed to leading innovation in nuclear medicine and delivering the next generation of targeted radioligand therapy to cancer patients. We are looking for an experienced Quality Leader to help us reach our ambitious goals.As the Global Quality...

SummaryTo lead the Ivrea TRD RLT Pilot plant Quality Control (QC) team by developing and executing strategic plans, providing direction for organizational structure, GMP and safety strategy, lean and continuous improvement initiatives, and people training and development. The QC Head is responsible for ensuring that the lab unit meets all agreed-upon...

SummaryTo lead the Ivrea TRD RLT Pilot plant Quality Control (QC) team by developing and executing strategic plans, providing direction for organizational structure, GMP and safety strategy, lean and continuous improvement initiatives, and people training and development. The QC Head is responsible for ensuring that the lab unit meets all agreed-upon...

Job Description: Scientific Project Manager - Drug DevelopmentLocation: Ivrea, ItalySalary: €110,000 - €140,000 per annumWe are seeking a highly skilled scientific project manager to lead the drug development process for our radioligand therapy team. As a key member of the team, you will be responsible for developing and implementing project strategies,...

At InnovHeart we are developing transcatheter mitral valve replacement (TMVR) systems to treat patients suffering from mitral valve disease. With a view to expanding the workforce and insourcing this role, we are looking for a Program manager who will be primarily responsible for the projects by integrating and coordinating the contributions of all the...

To lead the Ivrea TRD RLT Pilot plant Quality Control (QC) team by developing and executing strategic plans, providing direction for organizational structure, GMP and safety strategy, lean and continuous improvement initiatives, and people training and development. The QC Head is responsible for ensuring that the lab unit meets all agreed-upon objectives...

-Contributes, with appropriate oversight, to all aspects of global clinical trial(s) to deliver study outcomes within schedule, budget, quality/compliance and performance standards. May lead specific aspects of global clinical trial(s). Core member of the Clinical Trial Team, contributes to operational excellence through process improvement and knowledge...