deviation

1,737 deviation Stellenangebote in Schweiz. Täglich aktualisierte Angebote.


  • Basel City, Basel City, Schweiz Stracon Services AG Vollzeit

    pStracon Services AG sucht ab sofort einen Laborspezialisten zur Entwicklung und Optimierung von Labortätigkeiten in der biotechnologischen Wirkstoffproduktion im GMP-Umfeld. Sie unterstützen Produktionsschnittstellen, führen Troubleshooting im Labor durch und betreuen Laborausstattung sowie Sample Management. /ppSie arbeiten eigenverantwortlich an...


  • Lucerne, Canton of Lucerne, Schweiz Michael Page Vollzeit

    pMichael Page is seeking a Solution Supply Specialist for an international biotech company in Lucerne area. The role blends technical office work (deviation management, SOP/MES authoring, digitization) with hands-on Weigh Dispense and buffer/media preparation on the floor. /ppStart in October for a 12-month contract with extension option. The candidate will...


  • Basel, Basel City, Schweiz Hays Vollzeit

    bOverview /b pIn dieser Rolle arbeiten Sie eigenständig an der Entwicklung und Optimierung von Laborprozessen in der biotechnologischen Wirkstoffproduktion (GMP). Sie unterstützen Produktionsschnittstellen, sichern Prozessabläufe und leisten analysegestützte Troubleshooting-Unterstützung im Labor. Sie bedienen und warten Laborgeräte, verantworten...


  • Visp, Valais, Schweiz Lonza Vollzeit

    bOverview /b pIn this role you own quality-related responsibilities for daily qualification activities of facilities, equipment, and systems used in cGMP drug product manufacture. You will collaborate with cross-functional teams to ensure qualified states, manage deviations, CAPA, and documentation, and act as a SME driving quality standards. The position...


  • Lucerne, Canton of Lucerne, Schweiz Kinetics Process Consulting GmbH Vollzeit

    pKinetics Process Consulting GmbH is seeking experienced Commissioning, Qualification, and Validation professionals for pharmaceutical and biopharmaceutical projects in Switzerland. You will develop strategies, prepare and review lifecycle documentation, and provide technical leadership across the project lifecycle. /ppResponsibilities include supporting DQ,...

  • QA Validation Manager

    Vor 3 Tagen


    Visp, Valais, Schweiz ProClinical Vollzeit

    bOverview /b pIn this role you ensure GMP processes stay validated and compliant while supporting biotechnological manufacturing and cleaning validation. You will coordinate with cross-functional teams, auditors, and clients to provide scientifically sound evidence for product quality across the lifecycle. You act as the QA point of contact for validation...


  • Visp, Valais, Schweiz Lonza Vollzeit

    bOverview /b pIn dieser Position arbeiten Sie im QC-Bereich Small Molecules am Standort Visp und übernehmen ca. 50% Projektleitung. Sie koordinieren Projekte, führen Labortätigkeiten im Chromatographie-Labor und unterstützen den Methodentransfer. Sie erstellen und prüfen cGMP-Dokumente, führen Change Controls und Deviations durch und fördern das...


  • Zürich, Zürich, Schweiz Adryan Vollzeit CHF 90’000 - CHF 130’000 Vertrag

    Adryan is an internationally operating services group. From our offices in The Netherlands and Switzerland, we offer a full range of services for the life sciences industry. We are specialised in the areas of project management, engineering, CQV and compliance. Key responsibilities: Holds all quality related responsibilities for daily qualification...

  • QA Logistics Director

    Vor 2 Tagen


    Stalden (VS), Wallis, Schweiz Lonza Vollzeit CHF 180’000 - CHF 230’000 Vertrag

    Lonza is seeking an Associate Director, QA Logistics Functional Lead for Visp, Switzerland. The role provides strategic QA direction, prioritizes team activities, and acts as the primary escalation point for quality-related risks in logistics and infrastructure.Responsibilities include leading QA oversight for site logistics, deviations management, and...


  • Stein, Aargau, Schweiz Lonza Vollzeit CHF 120’000 - CHF 150’000 Vertrag

    Lonza Stein, AG Switzerland, is seeking a Supplier Quality professional to drive qualification activities for GMP-relevant materials, services, and equipment across Basel and Stein, integrating with Supply Chain, Manufacturing, QC, and Engineering.You will be the primary Quality contact for supplier qualification, review complex documentation, and manage...


  • Visp, Valais, Schweiz Lonza Vollzeit

    bOverview /b pAs a Subject Matter Expert for Drug Product, you provide frontline technical support on the shop floor under cGMP guidelines and drive improvements in manufacturing processes. You collaborate with manufacturing, engineering, and QA to troubleshoot and resolve issues, ensuring safe, compliant, on-time batch execution. You will own documentation,...

  • Junior Process Expert

    Vor 2 Tagen


    Stein, Aargau, Schweiz Novartis Farmacéutica Vollzeit CHF 74’000 - CHF 138’000 Vertrag

    Novartis is seeking a Junior Process Expert at our Stein site. The role focuses on supporting the Production Unit in improving processes, both qualitatively and quantitatively, while complying with cGMP and SOP guidelines.Major responsibilities include handling deviations and CAPAs, assisting in manufacturing instructions, quality notifications, and SOP...


  • Zug, Canton of Zug, Schweiz Madrigal Pharmaceuticals Vollzeit

    pMadrigal is seeking a senior professional to lead API supply oversight, continuity planning, and governance across external manufacturing partners. You will align demand, capacity, lead times, and inventory strategy into execution plans with sites/CMOs and manage risk and recovery actions. /ppIn this role, you will partner with CMC/MSAT/Quality to manage...


  • Visp, Wallis, Schweiz Lonza Vollzeit CHF 65’000 - CHF 85’000 Vertrag

    A global leader in life sciences is seeking a Senior Operator/Biotechnologist to support production in Visp, Switzerland. The ideal candidate will have a background in chemical or biopharmaceutical education, professional experience in pharmaceutical production, and be fluent in English. This role involves compliance with safety regulations, deviation...


  • Zürich, Zürich, Schweiz CLEEVEN Vollzeit CHF 90’000 - CHF 130’000 Vertrag

    CLEEVEN in Switzerland is seeking a Senior HPLC / Analytical Scientist to provide hands-on expertise and support our analytical activities on a long-term basis.You will install, calibrate, and maintain HPLC systems, perform data analysis and interpretation, assess results for deviations, troubleshoot methods, and contribute to method optimisation. Fluent...


  • Wallis, Wallis, Schweiz CTC Resourcing Solutions Vollzeit CHF 120’000 - CHF 180’000 Vertrag

    CTC is seeking a Senior Qualification Specialist for a contract position till end of March 2027 in the Valais region, Switzerland. Develop and maintain commissioning and qualification documents for new plants, including PQs for critical systems, and support ongoing validation post-implementation.Candidate will coordinate between internal teams and external...


  • Oberwallis, Wallis, Schweiz Gi Group Vollzeit CHF 120’000 - CHF 180’000 Vertrag

    Gi Group is seeking a QA Validation Manager to ensure critical GMP processes are validated and maintained in accordance with product requirements, process parameters, and global regulatory guidelines. The role partners with MSAT, Manufacturing and clients to provide scientifically sound, documented evidence that processes perform as required.The candidate...


  • , Schweiz Habasit Remote Vollzeit CHF 65’000 - CHF 90’000 Vertrag

    Habasit in Reinach is seeking several motivated and experienced machine operators for a 3-shift system. You will set up and start complex production equipment, monitor processes, and take corrective actions when deviations occur.You will ensure quality control and document results while handling internal transport with forklift trucks. The role requires...


  • Basel, Basel-Stadt, Schweiz Lonza Vollzeit

    pLonza Basel is seeking an experienced quality compliance specialist in analytical chemistry to drive compliance and operational excellence within our QC laboratories supporting biopharmaceutical manufacturing. /ppYou will lead end-to-end deviation investigations, root-cause analysis (RCA) and CAPA plans, write and manage Quality Change Requests, and act as...


  • Luzern, Luzern, Schweiz Kinetics Process Consulting GmbH Vollzeit CHF 100’000 - CHF 160’000 Vertrag

    Kinetics Process Consulting GmbH is seeking experienced Commissioning, Qualification, and Validation professionals for pharmaceutical and biopharmaceutical projects in Switzerland. You will develop strategies, prepare and review lifecycle documentation, and provide technical leadership across the project lifecycle.Responsibilities include supporting DQ, IQ,...