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Quality Assurance Associate I (80%)

​ Experis® is a global leader in IT professional resourcing, permanent recruitment, project solutions, and managed services. With over 25 years of experience in Switzerland and offices in Zürich, Basel, and Geneva, we connect top IT talent with leading companies. Our mission is to help professionals unlock their potential and thrive in dynamic, future-ready careers. ​ As a Quality Assurance Associate, you will contribute to maintaining and strengthening the Quality Management System at the Solothurn site. In this role, you'll support core quality activities, help coordinate routine governance processes, and assist in maintaining inspection readiness. You will collaborate with various site or global functions to ensure smooth execution of essential quality tasks. This position allows you to play an important part in sustaining a strong culture of compliance without carrying full ownership of operational responsibilities. The holder of this position will be responsible for the following activities: 1. Audit and Inspection Support - Coordinate and monitor audit and inspection commitments to ensure timely closure and proper documentation in line with Biogen QMS requirements. - Organize and facilitate meetings with SMEs to review action status, gather updates, and maintain alignment on deliverables. 2. Site Meeting Governance - Schedule and manage logistics for site governance meetings (e.g., Investigation Review Board), including agenda preparation, pre‑read collection, and documentation of decisions. - Support governance forums related to deviations, change controls, CAPAs, and other QMS review boards to ensure consistent application of Biogen standards. - Contribute to improving and optimizing governance meetings in line with site objectives 3. Self‑Inspection Program Execution - Assist in planning, implementing, and tracking the Self‑Inspection Program, including scheduling activities with SMEs and ensuring timely documentation and follow‑up of observations. - Maintain tools and trackers supporting inspection readiness and compliance monitoring. 4. QMS Administration & Operational Support - Support QMS processes including deviations, CAPAs, change controls, training assignments, and quality risk management in accordance with Biogen procedures. - Collaborate with cross‑functional stakeholders (QA, QC, Manufacturing, Engineering, etc.) to ensure compliance and timely completion of required actions. - Support on KPIs reporting and monitoring 5. Documentation & Data Management - Ensure accurate and compliant documentation of QMS activities in systems such as TrackWise, Veeva, and myCIMS. - Maintain logs, trackers, meeting minutes, dashboards, and metrics related to QMS processes and governance activities. - Identify opportunities to streamline QMS processes, improve documentation quality, and enhance visibility of compliance commitments. This position requires co-operation with people at every level of the organization and from multiple functions, including engineering, automation, validation, Manufacturing personnel, SME's on equipment and knowledge of biotechnology API production. Good communication skills in English, verbally and written. Self-driven and take ownership and responsibility for own assignments. Value teamwork at all levels, performs work with an open-mind and ability to value input from colleagues and peers. Able to drive discussion to solve problems with cross functional teams. Be confident in making technical decisions. In addition, must be able to prioritize tasks, be flexible and able to keep many activities running at a time.   ​ If you are interested in this opportunity, we look forward to receiving your CV or if you have any questions, contact Elaine Kanwar at +41 61 282 22 23. Check out all open positions at Experis at www.experis.ch Due to Swiss work permit restrictions, we can only consider applications from EU citizens or holders of valid working permit in Switzerland.

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30/09/2026

Quality Assurance Associate III

​ The role: The Associate III within the Integrated Downstream Quality Operations team is being part of the Quality Department at the new Large-Scale Manufacturing facility located at the Solothurn/Switzerland site. He/She focuses on Quality Operations and Quality Engineering activities for downstream manufacturing and equipment. The Solothurn site is intended to operate with a fully integrated electronic batch record for all commercial, clinical and PPQ campaigns. ​ General Information:  Start Date: 01.11.2026 End Date: 31.03.2027 (extension planned) Location: Solothurn Department: Quality Assurance, Integrated Downstream Quality Operations Responsibilities: - Executes QA activities related to downstream operations, GMP manufacturing,  and downstream equipment to ensure the safety, efficacy and purity of the products manufactured by Biogen - Reviews and approves GMP Engineering and Manufacturing documents during both project and operational phases of the site, specifically related to procedures, work instructions, CAPAs, deviations, change control, equipment (work orders, P&IDs, qualification protocols, calibration deviations..,) etc. - Partners with Manufacturing, Manufacturing Sciences, Process Engineering, Automation SMEs during deviation management and investigations. - Take part to the monitoring and release activities for Column Packing / Unpacking and Chromatography Review. - Ensures adherence to internal procedures during downstream manufacturing operations or for equipment controls and release before and during GMP CAPEX and OPEX project (i.e., shutdowns, construction projects) or New product introduction - Take part of the Quality On-Call duty rotation for Quality  - Participates in batch record review and close out in the view of batch release. - Experience with Quality Assurance, Equipment Qualification, Downstream Process is preferred. - Demonstrated ability to work autonomously with cross-functional team members. - Strong presentation and organizational skills - Demonstrated writing skills - Demonstrated problem solving skills - English B1 as a minimum. ​ If you are interested, please apply with a copy of your CV.  

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18/09/2026

IT OT Quality Systems Specialist

​ Experis® ist ein weltweit führender Anbieter von IT-Personalvermittlung, Festanstellungen, Projektlösungen und Managed Services. Mit über 25 Jahren Erfahrung in der Schweiz und Standorten in Zürich, Basel und Genf verbinden wir führende Unternehmen mit erstklassigen IT-Fachkräften. Unsere Mission ist es, Talente dabei zu unterstützen, ihr Potenzial zu entfalten und erfolgreiche, zukunftsorientierte Karrieren zu gestalten. ​ In dieser Funktion stellen Sie mit Ihren Kollegen sicher, dass die Stammdaten die behördlichen Anforderungen abdecken sowie die Arbeitsabläufe der Kunden reflektieren. Durch den 1st Level Support tragen Sie entscheidend dazu bei, die Lead Time hinsichtlich der Produktion und Freigabe von Produkten einzuhalten. Allgemeine Informationen: - Startdatum: asap - Spätestmögliches Startdatum: 1.12.2026 - Geplante Dauer der Anstellung:12 Monate - Verlängerung (bei Befristung): wahrscheinlich (bei genehmigtem Budget, Projektverlängerung,...)  - Arbeitsplatz: Basel oder Kaiseraugst - Workload: 100% - Home Office: Nach Onboarding Minimum 50% On-site Pflicht Aufgaben & Verantwortlichkeiten: - 1st Level Support für SingleLIMS bei stammdaten-relevanten Anfragen im eigenen Verantwortungsbereich - Neuaufnahme, Anpassung und Review von Stammdaten und Methoden entsprechend den Bedürfnissen der Kunden bzw. der behördlichen Anforderungen - Review von Probenahmepläne und Kommunikation von Requirements an das Business - Erstellen und Aktualisieren von Konzepten, Arbeitsanweisungen (SOPs) und anderen relevanten GMP-Dokumenten - Schnittstelle zwischen dem Kunden (Business) und global IT (Entwickler, 2nd/3rd Level Support) Must Haves: - Voraussetzung für die abwechslungsreiche Stelle ist ein abgeschlossenes Studium in den relevanten Bereichen (z.B. Pharma, Chemie, Verfahrenstechnik)  - Mindestens 1-3 Jahre Berufserfahrung im GMP Umfeld (vorzugsweise in den Bereichen Produktion oder Qualitätskontrolle) - Praxiserfahrung im Bereich der pharmazeutischen Herstellungsanalytik (IPC / QC) - Erfahrung mit der Pflege von Stammdaten im GMP Umfeld z.B. mit LIMS (Labware), MES, ERP  - Selbstständige, strukturierte, und proaktive Arbeitsweise, präzise Arbeit unter strengen Timelines und multiplen parallelen Aufgaben - Kommunikative und organisatorische Fähigkeiten und ein selbstsicheres Auftreten - Hohe Kunden- / Serviceorientierung - Sehr gute Deutsch Kenntnisse in Wort und Schrift (C1) ​​​​​​​Nice to Haves: - Grundkenntnisse von internen Systemen und Projektmanagement sind von Vorteil - Erfahrung im Bereich Business Analytics im GMP Manufacturing oder QC Umfeld - Englischkenntnisse in Wort und Schrift   ​ Weitere Schritte Interviews: 1 Runde On-site (wenn möglich) und 2te Runde Virtuell Klingt das nach der richtigen Herausforderung für dich? Wir freuen uns auf deine Bewerbung!     APPLY NOW • Interviews: 1 Runde On-site (wenn möglich) und 2te Runde Virtuell

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08/10/2026

Quality Control Analyst

​ Quality Control Analyst Start date: asap Duration: 9 months Location: Neuchatel ​ Vous apportez une expérience solide de laboratoire, y compris des méthodes biochimiques telles que ELISA, PCR. activité enzymatique, Western Blot, HPLC ou autre. Grâce à votre travail en tant que technicien de laboratoire, vous avez développé une bonne compréhension théorique et pratique des méthodes et de la technologie biochimiques. En particulier, nous attendons : - Vous travaillez de manière structurée et dans un souci de qualité. - Vous trouvez satisfaction et motivation dans les tâches routinières - Vous avez de l'expérience en matière de bonnes pratiques de fabrication (cGMP) et laboratoire controle qualité en industrie pharmaceutique Nous privilégions un environnement de proximité et détendu. Le travail s'effectue au sein d'une  équipe où les tâches changent très rapidement. On attend donc de vous que vous soyez motivé par un environnement en évolution rapide tout en étant capable de fournir des résultats de haut niveau. Missions principales : - Réaliser les activités d'analyses biochimique et de supervision selon les procédures en vigueur au laboratoire en respectant les règles GMP/BPD et/ou des projets en lien avec les activités du département Contrôle Qualité - Préparer des solutions utilisées pour nos analyses de laboratoire - Respecter l'ensemble des procédures en vigueur - Respecter et appliquer les règles EHS. - Renseigner les divers formulaires, logbooks et documents en respectant les Bonnes Pratiques de Fabrication et de Documentation et ALCOA + - Prévenir le Superviseur en cas de résultats non conformes et/ou invalides le jour même par oral et/ou écrit et initier l'évènement dans le système qualité dans les délais impartis. - Gérer les investigations laboratoires. - Appliquer les demandes planning et remonter tout soucis de manière proactive. - Exécuter les protocoles de qualifications des réactifs / consommables et de validation (méthode, système, équipements) - S'assurer que la calibration et la maintenance des équipements est en ordre lors de l'analyse - Respecter la gestion des Kanban en temps réel - Remonter au responsable de méthode/équipement et au Superviseur/délégué/Expert des écarts sur la procédure - Être capable d'identifier et résoudre certains problèmes peu complexes relatifs à son domaine d'expertise (Troubleshooting) - Réalisez les solutions ou approbation des solutions au laboratoire. - Gérez et ranger le laboratoire en général, respecter les normes de standardisation 5S.  - Supporter les initiatives d'amélioration continue Profil recherché : - Niveau d'études minimum : CFC laboratin/biologie ou un autre domaine scientifique pertinent. - 3 ans d'expérience minimum en laboratoire QC en environnement cGMP - Expérience en analyse Electrophorèse, HPLC, Elisa, ou en détermination de l'activité enzymatique souhaité - Francais courant et anglais technique - Nationalité suisse ou de l'UE, ou encore permis de travail suisse valide - Expérience en rédaction de protocole de validation de méthode est ​ If you are interested, please apply with your CV 

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07/10/2026

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Solothurn, Soloithurn