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Jobdetails

Zusammenfassung

    veröffentlicht am 24. april 2026

    Referenznummer
    25044
    nimm Kontakt mit uns auf

    Wir sind hier, um dir bei deinen Fragen zu helfen.

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    Walentyna Dobrowolska

    +41 58 201 56 71

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    Jobdetails

    For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a QC/QA E2E Digital Expert (Application Support).

    General Information:

    • Start Date: 01.07.2026
    • Latest possible start date: 01.08.2026
    • Planned Employment Duration: 12 months contract with the possibility of extension (depending on the performance)
    • Workplace: Kaiseraugst
    • Workload: 100%
    • Home Office: by arrangement
    • Department: Unit QC Application Support (MMQIAB8I)
    • Working Hours: Standard

    About the job:

    The "Digital Backbone of Quality Control" department is a new division within Quality Control Basel/Kaiseraugst with approximately 30 employees, organized into two teams and subject matter experts. This unit focuses on master data management, application support, and BPM (Business Process Manager) and BPO (Business Process Owner) tasks within the digital QC systems.

    As a QC E2E Digital Expert (application support), you will be part of the application support team and responsible for supporting all digital systems of Quality Control Basel/Kaiseraugst (e.g., NEXTLab, LabX, EMPOWER, etc.). This is crucial for ensuring the conformity of our products.

    The perfect candidate:

    We are looking for someone with several years of experience in the pharmaceutical industry (QA/QC), ideally with IT systems knowledge (especially Waters EMPOWER 3, including the creation and maintenance of custom fields). You impress with strong influence, motivation, and negotiation skills, as well as excellent networking abilities. As a team player, you promote cross-functional collaboration, drive continuous improvement, and challenge the status quo. You communicate and present confidently, think analytically and solution-oriented, and possess a strong business acumen and an end-to-end mindset. Fluent German and very good English skills complete your profile.

    Tasks & responsibilities:

    • Compliance with GxP regulations
    • Compliance with HSE regulations
    • Compliance with LPS elements (behaviors, improvement process, etc.)
    • Compliance with internal guidelines
    • Creation and maintenance of GMP documentation
    • Ensuring the timely and high-quality execution of tasks within the area of responsibility
    • Support of EMPOWER, including incident management, documentation, and reporting
    • Operational support of all local laboratory systems within Commercial QC Basel/Kaiseraugst, including incident management, documentation, and reporting
    • Maintenance of local master data (EMPOWER 3, including custom fields)
    • Consulting role based on specific system and process expertise (SME activities)
    • Reporting and data analysis
    • Audit support for all local laboratory systems
    • Participation in audits/self-inspections (including request presentations)

    Must-haves:

    • Preferably 3+ years of experience in the pharmaceutical industry in the area of quality assurance or quality control
    • Preferably experience in IT systems (especially EMPOWER 3, including the creation and maintenance of custom fields) within the pharmaceutical industry
    • Excellent skills in influencing, motivating, and negotiating at all levels.
    • Excellent networking skills
    • Team player with a focus on cross-functional collaboration
    • Focus on continuous improvement
    • Courage to challenge the status quo
    • Partner with the ability to command authority in a global environment
    • Excellent communication and presentation skills
    • Conceptual, analytical, and solution-oriented thinking and approach
    • Broad understanding of the business and an end-to-end mindset
    • Fluency in German and very good in English.

    Sounds interesting? Apply now – we’re looking forward to receiving your applications!

    Application Submission Deadline: 04.05.2026

    ...

    For one of our clients, a global pioneer in pharmaceuticals, we are currently looking for a QC/QA E2E Digital Expert (Application Support).

    General Information:

    • Start Date: 01.07.2026
    • Latest possible start date: 01.08.2026
    • Planned Employment Duration: 12 months contract with the possibility of extension (depending on the performance)
    • Workplace: Kaiseraugst
    • Workload: 100%
    • Home Office: by arrangement
    • Department: Unit QC Application Support (MMQIAB8I)
    • Working Hours: Standard

    About the job:

    The "Digital Backbone of Quality Control" department is a new division within Quality Control Basel/Kaiseraugst with approximately 30 employees, organized into two teams and subject matter experts. This unit focuses on master data management, application support, and BPM (Business Process Manager) and BPO (Business Process Owner) tasks within the digital QC systems.

    As a QC E2E Digital Expert (application support), you will be part of the application support team and responsible for supporting all digital systems of Quality Control Basel/Kaiseraugst (e.g., NEXTLab, LabX, EMPOWER, etc.). This is crucial for ensuring the conformity of our products.

    The perfect candidate:

    We are looking for someone with several years of experience in the pharmaceutical industry (QA/QC), ideally with IT systems knowledge (especially Waters EMPOWER 3, including the creation and maintenance of custom fields). You impress with strong influence, motivation, and negotiation skills, as well as excellent networking abilities. As a team player, you promote cross-functional collaboration, drive continuous improvement, and challenge the status quo. You communicate and present confidently, think analytically and solution-oriented, and possess a strong business acumen and an end-to-end mindset. Fluent German and very good English skills complete your profile.

    Tasks & responsibilities:

    • Compliance with GxP regulations
    • Compliance with HSE regulations
    • Compliance with LPS elements (behaviors, improvement process, etc.)
    • Compliance with internal guidelines
    • Creation and maintenance of GMP documentation
    • Ensuring the timely and high-quality execution of tasks within the area of responsibility
    • Support of EMPOWER, including incident management, documentation, and reporting
    • Operational support of all local laboratory systems within Commercial QC Basel/Kaiseraugst, including incident management, documentation, and reporting
    • Maintenance of local master data (EMPOWER 3, including custom fields)
    • Consulting role based on specific system and process expertise (SME activities)
    • Reporting and data analysis
    • Audit support for all local laboratory systems
    • Participation in audits/self-inspections (including request presentations)

    Must-haves:

    • Preferably 3+ years of experience in the pharmaceutical industry in the area of quality assurance or quality control
    • Preferably experience in IT systems (especially EMPOWER 3, including the creation and maintenance of custom fields) within the pharmaceutical industry
    • Excellent skills in influencing, motivating, and negotiating at all levels.
    • Excellent networking skills
    • Team player with a focus on cross-functional collaboration
    • Focus on continuous improvement
    • Courage to challenge the status quo
    • Partner with the ability to command authority in a global environment
    • Excellent communication and presentation skills
    • Conceptual, analytical, and solution-oriented thinking and approach
    • Broad understanding of the business and an end-to-end mindset
    • Fluency in German and very good in English.

    Sounds interesting? Apply now – we’re looking forward to receiving your applications!

    Application Submission Deadline: 04.05.2026

      nimm Kontakt mit uns auf

      Wir sind hier, um dir bei deinen Fragen zu helfen.

      W

      Walentyna Dobrowolska

      +41 58 201 56 71
      verwandte Jobsalle Spezialist Für Qualitätskontrolle Jobs in Kaiseraugst
      • QC Analyst Senior

        • Neuenburg, Neuenburg
        • Temporär
        <p>Dans le cadre de la mise en service d’un nouveau bâtiment de production, nous recherchons un(e) QC Analyst Senior pour renforcer l’équipe de notre client.</p><p> </p><p>Lieu : Neuchâtel</p><p>Période : du 01/05/2026 to 31/08/2026 (avec possibilité de prolongation)</p><p>Contrat : Temporaire via Randstad Professionals</p><p> </p><p>Description du poste :</p><p> </p><p>Le travail consiste à réaliser les activités d’analyses et de prélèvement dans le cadre de la construction d'un nouveau bâtiment de production.</p><p>Après une période de formation dense, les tâches demandées devront se dérouler dans le strict respect des procédures GMP en vigueur au laboratoire de contrôle et des consignes de sécurité en lien avec les activités du département Contrôle Qualité.</p><ul><li><p>Réaliser des analyses ou des approbations d’analyses au laboratoire QC selon les procédures et normes applicables, par exemple les cGMP et les pharmacopées, en fonction des priorités de planification</p></li><li><p>Respecter l’ensemble des règles décrites dans les SOP en application dans le laboratoire</p></li><li><p>Exécuter les activités du laboratoire avec la SOP en vigueur ouverte</p></li><li><p>Renseigner les divers formulaires, logbooks et documents en respectant les BPF et le(s) système(s) de gestion des résultats</p></li><li><p>Prévenir le Superviseur/délégué/Expert 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</p></li><li><p>Respecter et appliquer les règles EHS</p></li><li><p>Signaler toute déviation au planning de façon proactive</p></li><li><p>Exécuter les protocoles de qualification des réactifs / consommables</p></li><li><p>Participer aux validations (méthodes, systèmes, équipements)</p></li><li><p>Gérer les recalculs, les alarmes, les documents contrôlés, les équipements, les fournisseurs</p></li><li><p>Réaliser des GEMBA, soutenir les initiatives d’amélioration continue</p></li><li><p>Former les analystes, être backup pour la formation GMP</p></li><li><p>Gérer les déviations, OOL, CAPA, et participer aux inspections</p></li><li><p>Être le support pour les projets, soumissions réglementaires et analyses de risques</p></li></ul><p> </p><p>Compétences requises :</p> <ul><li><p>Être à l’aise avec les outils informatiques et bureautiques usuels (pack Office)</p></li><li><p>Français et Anglais (technique)</p></li><li><p>Anglais (B2 minimum)</p></li><li><p>Qualités personnelles:</p><ul><li><p>Être en adéquation avec les valeurs de l’entreprise (Honnêteté, Intègrité, Equité et Persévérance)</p></li><li><p>Être organisé</p></li><li><p>Avoir le sens du travail en équipe</p></li><li><p>Savoir communiquer efficacement et de manière approprié.</p></li><li><p>Avoir un comportement exemplaire</p></li><li><p>Être orienté patient</p></li></ul></li></ul><br />
        published on 9. April 2026
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