QA Deviations Specialist

**Summary**:The Deviations Specialist/ QA Investigator is responsible for managing and executing investigations of deviations and non-conformities within manufacturing and quality control environments. This role ensures root causes are identified, corrective and preventive actions (CAPAs) are implemented effectively, and documentation complies with cGMP and...

**Summary**: The Deviations Specialist/ QA Investigator is responsible for managing and executing investigations of deviations and non-conformities within manufacturing and quality control environments. This role ensures root causes are identified, corrective and preventive actions (CAPAs) are implemented effectively, and documentation complies with cGMP and...

**Summary**: The Deviations Specialist/ QA Investigator is responsible for managing and executing investigations of deviations and non-conformities within manufacturing and quality control environments. This role ensures root causes are identified, corrective and preventive actions (CAPAs) are implemented effectively, and documentation complies with cGMP and...

**Summary**:~Verwaltet Qualitätsaspekte und Projekte im Verantwortungsbereich.~Gewährleistet und unterstützt die GxP-Konformität und die Einhaltung der Qualitätsmanagementsysteme von Novartis.**About the Role**:Major Accountabilities~ Überwachung aller Produktions- und Testaktivitäten, Sicherstellung der Einhaltung von cGxP, inkl. Datenintegrität und...

**Summary**:~Gestiona aspectos de Calidad y proyectos dentro del área de responsabilidad.~ Garantiza y respalda la conformidad general de GxP y el cumplimiento de los sistemas de gestión de calidad de Novartis.**About the Role**:Major Accountabilities~ Supervisión de todas las actividades de producción y pruebas, garantiza el cumplimiento de cGxP,...

**Summary**:~Upravlja vidike kakovosti in projekte znotraj področja odgovornosti.~Zagotavlja in podpira splošno skladnost GxP in skladnost z Novartisovimi sistemi vodenja kakovosti.**About the Role**:Major Accountabilities~ Nadzor nad vsemi proizvodnimi in testnimi aktivnostmi, zagotavlja skladnost s cGxP, vključno s celovitostjo podatkov in...

**Summary**:~Gérer les aspects et les projets de qualité dans le domaine de responsabilité.~ Assure et soutient la conformité globale GxP et la conformité aux systèmes de gestion de la qualité de Novartis.**About the Role**:Major Accountabilities~ Supervision de toutes les activités de production et de test, assure la conformité avec cGxP, y compris...

**Summary**:~責任範囲内で品質面とプロジェクトを管理します。~全体的なGxP適合性とノバルティス品質管理システムへの準拠を保証およびサポートします。**About the Role**:Major Accountabilities~

**Summary**: - Responsable de la preparación del Informe Anual de Revisión de Calidad del Producto (APQR/PQR) para los productos comercializados de Novartis de acuerdo con los requisitos de la compañía y regulatorios, o informe anual similar/equivalente requerido por las autoridades sanitarias. - Responsable de la extracción y compilación de datos...

**Summary**:- Assurance that the product quality conforms with specifications and that production activity is compliant with Novartis quality policy and GxP requirements. Ensure that relevant documentation is up-to-date and archived correctly. Ensure “state of the art” GxP know-how and future trends in the field of GxP**About the Role**:**Major...