Join a fast-growing Bioplant in Yverdon-les-Bains during a pivotal expansion phase. We are seeking a QA QC Expert to ensure the highest quality standards for our Drug Substances and Raw Materials.ResponsibilitiesBatch Disposition: Collect and review all records for Drug Substance (DS) and Drug Product (DP) release; chair weekly disposition meetings.QA Oversight of QC: Provide day-to-day quality guidance to the lab, approving specifications, analytical
Spécialiste Assurance Qualité Opérations – BiotechnologieCanton de VaudPoste Temporaire (Jusqu'à fin 2026)Vous êtes un expert de la qualité qui s’épanouit sur le terrain ? Vous parlez le même langage que les équipes de production ? Mission Intégré aux flux de production (USP, DSP, Buffer & Media Prep), vos responsabilités sont les suivantes :Partenaire de terrain : Assurer la supervision quotidienne des activités (zones de lavage, préparation, culture et
Spécialiste Support Production / Déviations (USP/DSPEntreprise : Incyte (Yverdon-les-Bains)Type de poste : Temporaire (jusqu'à la fin de l'année)Horaires : De journéeLocalisation : Nord Vaudois Pour le site de production pharmaceutique de notre client, nous recherchons un Spécialiste Support Production. Vous serez l'expert des opérations et de la qualité.Votre bureau ? Le shopfloor.Votre quotidien ? Être au plus près des bioréacteurs (USP), des colonnes
Senior Specialist / QA Manager (CMO Operations – Small Molecules)Location: Morges, Switzerland (Up to 2 days of remote work per week) Contract Type: Temporary – Starting ASAP (possibility of extension)Language: Fluent English (C1) required Due to a significant increase in our client activities, we are looking for a Senior Specialist or QA Manager to reinforce a dynamic team of 4 people.This role is 100% focused on managing the Contract Manufacturing
Position Snapshot Location: Vers-chez-les-Blanc, SwitzerlandEntity: Clinical Research Unit, Nestlé ResearchWork rate: 100%Contract type: TemporaryDuration: 12 monthsSummaryThe Senior Clinical Trial Assistant (Sr. CTA) provides high-quality operational and administrative support to clinical trial teams throughout all phases of a pharmaceutical study. Operating within a fast-paced, regulated environment, the Sr. CTA ensures clinical documentation is
17. Febbraio 2026
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