For our client based in Vaud canton and specialized in biopharmaceutical area, we’re looking for a Senior Quality Assurance - CSV specialist ResponsabilityManage Quality oversight for computerized systems validation and the data integrity program & support QA activities for system introduction/upgrades, ensuring compliance with quality policies, cGMP, EU/US, and Swiss regulations.Oversee daily quality for GxP IT, CSV, and automated systems (SISA).Act as th
For our client based in Vaud canton and specialized in biopharmaceutical area, we’re looking for a Senior Quality Assurance - CSV specialist ResponsabilityManage Quality oversight for computerized systems validation and the data integrity program & support QA activities for system introduction/upgrades, ensuring compliance with quality policies, cGMP, EU/US, and Swiss regulations.Oversee daily quality for GxP IT, CSV, and automated systems (SISA).Act as th
For our client Merck in Aubonne, we are looking for a QA Specialist for QC (m/f/d) for a period of 12 months from 1st September 2024.Your role: To ensure the quality oversight and compliance of QC activities and the data integrity of QC analytical data in timely manner. QA Oversight on QC analytical data:To perform the QA review on QC analytical data, on QC documentation. Manage QC deviation, CCP and CAPA as QA.Compliance of QC activities:QA support for QC
For our client Merck in Aubonne, we are looking for a QA Specialist for QC (m/f/d) for a period of 12 months from 1st September 2024.Your role: To ensure the quality oversight and compliance of QC activities and the data integrity of QC analytical data in timely manner. QA Oversight on QC analytical data:To perform the QA review on QC analytical data, on QC documentation. Manage QC deviation, CCP and CAPA as QA.Compliance of QC activities:QA support for QC
Nous sommes à la recherche d’un.e QA Release Coordinator pour notre client, Merck, pour une mission d’une durée de 12 mois. Vos missions :Assurer la revue de la documentation liée aux produits intermédiaires (Produit semi-finis et diluants, internes et externes) sur les sites d’Aubonne afin qu’elle satisfasse aux critères des cGMPs, aux dossiers d’enregistrement et aux systèmes de qualité de la société.Assurer la préparation de la documentation pour la lib
Nous sommes à la recherche d’un.e QA Release Coordinator pour notre client, Merck, pour une mission d’une durée de 12 mois. Vos missions :Assurer la revue de la documentation liée aux produits intermédiaires (Produit semi-finis et diluants, internes et externes) sur les sites d’Aubonne afin qu’elle satisfasse aux critères des cGMPs, aux dossiers d’enregistrement et aux systèmes de qualité de la société.Assurer la préparation de la documentation pour la lib