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Job details

Summary

    Posted 1. april 2026

    Reference number
    24880
    get in touch

    we are here to help you with your questions.

    M

    Margot Ferraton

    +41 58 201 54 41

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    Job details
    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.
    ...
    Responsibilities
    • Batch 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 methods, and sampling plans.
    • Operational Quality: Lead QA activities for method transfers/validations and support the commissioning of new lab equipment.
    • Quality Events: Manage Deviations, OOS (Out of Specification), OOT (Out of Trend), and Change Controls.
    • Project Support: Contribute to the implementation of raw material testing and new sterility tests.
    • Systems: Review LIMS master data changes and support computerized system integration.

    Profile
    • Education: Academic degree in Biotechnology, Pharmacy, Bioprocessing, or a related field.
    • Experience: Minimum 5 years in a GMP environment.
    • Industry Expertise (Mandatory): Solid experience in Biotech or Vaccines (Antibodies/Proteins).
    • Technical Hybrid: Strong background in Quality Control (hands-on or oversight) transitioned into QA.
    • Methods: Demonstrated experience in analytical method validation and transfer.
    • Systems (Plus): Experience with LIMS (configuration or data review) is a significant advantage.
    • Soft Skills: Pragmatic decision-maker, team player, and excellent communicator.
    • Languages: Fluency in English and French is required.


    Profiles from Medical Devices or Solid Dosage will not be considered.
    Show more
    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.

    Responsibilities
    • Batch 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 methods, and sampling plans.
    • Operational Quality: Lead QA activities for method transfers/validations and support the commissioning of new lab equipment.
    • Quality Events: Manage Deviations, OOS (Out of Specification), OOT (Out of Trend), and Change Controls.
    • Project Support: Contribute to the implementation of raw material testing and new sterility tests.
    • Systems: Review LIMS master data changes and support computerized system integration.
    ...
    Profile
    • Education: Academic degree in Biotechnology, Pharmacy, Bioprocessing, or a related field.
    • Experience: Minimum 5 years in a GMP environment.
    • Industry Expertise (Mandatory): Solid experience in Biotech or Vaccines (Antibodies/Proteins).
    • Technical Hybrid: Strong background in Quality Control (hands-on or oversight) transitioned into QA.
    • Methods: Demonstrated experience in analytical method validation and transfer.
    • Systems (Plus): Experience with LIMS (configuration or data review) is a significant advantage.
    • Soft Skills: Pragmatic decision-maker, team player, and excellent communicator.
    • Languages: Fluency in English and French is required.


    Profiles from Medical Devices or Solid Dosage will not be considered.
    Show more
      get in touch

      we are here to help you with your questions.

      M

      Margot Ferraton

      +41 58 201 54 41
      related jobs.all Quality Assurance Specialist jobs in Yverdon-les-Bains
      • Spécialiste Support Production / Déviations (USP/DSP)

        • Yverdon-les-Bains, Vaud
        • Temporary
        <p>Spécialiste Support Production / Déviations (USP/DSP</p><p>Entreprise : Incyte (Yverdon-les-Bains)<br />Type de poste : Temporaire (jusqu'à la fin de l'année)<br />Horaires : De journée<br />Localisation : Nord Vaudois</p><p> </p><p>Pour le site de production pharmaceutique de notre client, nous recherchons un Spécialiste Support Production.</p><p> </p><p>Vous serez l'expert des opérations et de la qualité.<br />Votre bureau ? Le shopfloor.<br />Votre quotidien ? Être au plus près des bioréacteurs (USP), des colonnes de chromatographie, des systèmes UFDF et de nanofiltration pour garantir que chaque lot produit est une réussite.</p><p> </p><p> </p><p>Responsabilités</p><ul><li>Spécialiste production : Lorsqu'un écart survient en plein milieu d'une culture cellulaire ou d'une purification, vous êtes sur place. Vous enquêtez en direct avec les opérateurs, analysez l'impact technique et proposez des solutions immédiates.</li><li>Maître de la Conformité Opérationnelle : Vous pilotez les déviations et les CAPA. Votre objectif ? Comprendre le "pourquoi" (Root Cause) pour que le problème ne revienne jamais.</li><li>Expert Technique (SME) : Vous participez à l'amélioration continue des équipements et des processus. Lors des audits, c’est vous qui présentez avec fierté la robustesse des investigations.</li><li>Amélioration Continue : Vous révisez les Batch Records et les SOP pour les rendre plus simples, plus sûrs et plus efficaces pour les équipes de fabrication.</li></ul><p> </p><p> </p><p>Profil</p><ul><li>Formation : Du CFC (technologue en production de chimie/biotech) au Master (Ingénieur Biotech/Pharma). C’est votre expérience et votre compétence technique qui priment.</li><li>Expérience : Vous avez au moins 3 ans d'expérience en production Biotech (obligatoire). Vous connaissez le jargon USP/DSP et la réalité des zones classées.</li><li>Savoir-être : Vous êtes "moteur". Vous n’attendez pas qu’on vous donne une tâche, vous allez au-devant des problèmes. Vous savez communiquer avec pédagogie auprès des opérateurs et avec fermeté auprès de la Qualité.</li><li>Langues : Français courant. L’anglais (niveau B2) est indispensable pour les rapports de déviations.</li></ul>
        published on April 28, 2026
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