5 Qualité Et Contrôle emplois trouvés pour toi.

Selezioniamo per azienda certificata nel settore aeronautico un Responsabile della qualità :In qualità di Responsabile Qualità i suoi compiti principali sono:- Gestire il Sistema Qualità al fine di mantenere le certificazioni ottenute ed attuare ilmiglioramento continuo dell'Azienda;- Mettere a punto e mantenere aggiornati, in collaborazione con i Responsabili delle differenti Funzioni, i documenti del Sistema Qualità;- Redigere e mantenere aggiornato il

For one of our clients, an international pharmaceutical company, in the canton of Neuchâtel, we are seeking aBulk Manufacturing ManagerContract: Permanent (CDI)A unique opportunity to contribute to the manufacturing of high-quality pharmaceutical products in a stimulating and innovative environment!Your role:Oversee daily Bulk team management, ensuring timely delivery.Develop and manage the Bulk Operations team, encompassing manufacturing, planning, and

For our client, a leading pharmaceutical company in Switzerland, we are looking for an IMP Quality Manager.General Information: Start date: ASAPLatest possible start date: 01.09.2025Duration: 12 months, with the possibility of extensionWorkplace: BaselWorkload: 80-100%Remote/home office: max 20%Team: 10 peopleDepartment: IMP Quality Operations Basel&Kau (MMQIE)Working hours: StandardAbout the work:IMP Quality Operations Switzerland is responsible for

For our client, a leading biotechnology company, we are looking for a Manufacturing Associate II to support upstream processing.General Information:Start date: ASAPEnd date: 31.01.2026, with the possibility of extension.Workplace: Luterbach, SolothurnWorkload: 100%Remote/Home office: Not availableAbout the job:As a Manufacturing Associate (MA), you will perform and document daily manufacturing operations in a cGMP environment. Your responsibilities

QA/RA Spécialiste – Qualité Distribution Internationale Poste temporaire jusqu’à la fin de l’année Basé à : Morges  Résumé du poste :Ce poste consiste à s’assurer que les médicaments de l’entreprise sont distribués dans le monde dans le respect des règles de qualité et des exigences réglementaires. La personne travaille sur les dossiers d’autorisation (GMP), suit la qualité des partenaires de distribution, et soutient l’ouverture de nouveaux