QC Associate, Analyst

lonza· CH12 Lonza AG
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📍 CH - VispFull time

About this role

 

Sofern erforderlich, steht berechtigten Kandidaten und ihren Familien Unterstützung beim Umzug zur Verfügung.

Du möchtest in einem anspruchsvollen GMP-Umfeld arbeiten und mit physikalisch-chemischen Analysen einen wichtigen Beitrag zur Produktqualität leisten? In unserem QC Chemical Physical Analytics Team übernimmst du Verantwortung für analytische Prüfungen, Laborgeräte und die kontinuierliche Verbesserung unserer Prozesse.

Das bieten wir dir:

  • Ein abwechslungsreiches Tätigkeitsfeld in einem modernen Laborumfeld.

  • Spannende Aufgaben mit direktem Einfluss auf Produktqualität und Patientensicherheit.

  • Moderne Technologien und analytische Methoden.

  • Möglichkeiten zur fachlichen und persönlichen Weiterentwicklung.

  • Ein engagiertes Team, das Zusammenarbeit, Offenheit und gegenseitige Unterstützung lebt.

Deine Aufgaben:

  • Durchführung, Auswertung und Dokumentation von physikalisch-chemischen Analysen gemäß cGMP-Anforderungen, regulatorischen Vorgaben und internen Richtlinien.

  • Sicherstellung einer GMP-konformen und termingerechten Bearbeitung von Analysenaufträgen.

  • Verantwortung für zugewiesene Laborgeräte, einschließlich Kalibrierungen, Qualifizierungen und der zugehörigen Dokumentation.

  • Unterstützung bei Troubleshooting-Aktivitäten sowie bei der Untersuchung von Abweichungen und der Umsetzung von Korrekturmaßnahmen.

  • Aktive Mitarbeit bei der Weiterentwicklung und Optimierung von Laborprozessen, Methoden und Arbeitsabläufen.

  • Unterstützung bei der Einarbeitung neuer Teammitglieder sowie beim Wissensaustausch innerhalb des Teams.

  • Teilnahme am Pikettdienst nach vorheriger Planung.

Dein Profil:

  • Abgeschlossene Ausbildung als Laborantin EFZ, Chemie-, Biologie- oder Pharmalaborantin oder eine vergleichbare naturwissenschaftliche Qualifikation.

  • Erste oder mehrjährige Berufserfahrung in der Qualitätskontrolle, vorzugsweise in einem GMP-regulierten Umfeld der Pharma-, Biotech- oder Chemieindustrie.

  • Erfahrung mit physikalischen und physikalisch-chemischen Analysen, beispielsweise:

    • pH-Messungen

    • Karl-Fischer-Titration

    • Proteinbestimmung mittels UV-Spektroskopie

    • Osmolalitäts- oder Leitfähigkeitsmessungen

  • Hohes Qualitätsbewusstsein sowie Verständnis für GMP- und Compliance-Anforderungen.

  • Strukturierte, eigenverantwortliche und lösungsorientierte Arbeitsweise.

  • Freude an Teamarbeit, Wissensaustausch und kontinuierlicher Verbesserung.

  • Gute Deutschkenntnisse sowie grundlegende Englischkenntnisse.

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The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

Are you looking to work in a challenging GMP-regulated environment and make a meaningful contribution to product quality through physical and physico-chemical testing? As part of our QC Physical Analytics team, you will take ownership of analytical testing, laboratory equipment, and the continuous improvement of our processes.

What you will get:

  • A diverse and rewarding role in a modern laboratory environment.

  • Meaningful work with a direct impact on product quality and patient safety.

  • Access to modern technologies and analytical techniques.

  • Opportunities for professional and personal development.

  • A collaborative team culture built on openness, respect, and mutual support.

What you will do:

  • Perform, evaluate, and document physico-chemical analyses in compliance with cGMP requirements, regulatory expectations, and internal procedures.

  • Ensure the timely and GMP-compliant execution of assigned testing activities.

  • Take responsibility for designated laboratory equipment, including calibration, qualification, and associated documentation.

  • Support troubleshooting activities, deviation investigations, and the implementation of corrective actions.

  • Actively contribute to the development and optimization of laboratory processes, analytical methods, and workflows.

  • Support the onboarding and training of new team members and promote knowledge sharing within the team.

  • Participate in the on-call duty rota as scheduled.

What we are looking for:

  • Completed apprenticeship or degree in Chemistry, Biology, Pharmaceutical Sciences, or a comparable scientific discipline.

  • Initial or several years of experience in Quality Control, ideally within a GMP-regulated pharmaceutical, biotech, or chemical manufacturing environment.

  • Experience with physical and physico-chemical analytical techniques, such as:

    • pH measurements

    • Karl Fischer titration

    • UV spectroscopy for protein concentration determination

    • Osmolality and conductivity measurements

  • Strong quality mindset and understanding of GMP and compliance requirements.

  • Structured, independent, and solution-oriented way of working.

  • Enjoy working collaboratively and contributing to continuous improvement initiatives.

  • Good command of English and basic German skills.

    About Lonza

    At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.

    Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

    Ready to shape the future of life sciences? Apply now.

    Frequently Asked Questions

    Is the salary disclosed for the QC Associate, Analyst position at lonza?
    The salary for this QC Associate, Analyst role at lonza is not publicly listed. Click "Apply Now" to learn more about the compensation package on their official careers page.
    Where is the QC Associate, Analyst position at lonza located?
    This QC Associate, Analyst role at lonza is based in CH - Visp. The position is listed as on-site or hybrid. Check the full job description or apply directly to confirm the work arrangement.
    Is the QC Associate, Analyst role at lonza full-time or part-time?
    This is listed as a Full time position. It is posted as a QC Associate, Analyst role in the CH12 Lonza AG department at lonza.
    Which team or department does the QC Associate, Analyst at lonza belong to?
    This QC Associate, Analyst position is part of the CH12 Lonza AG department at lonza. See the full job description for more information about the team structure and responsibilities.
    How do I apply for the QC Associate, Analyst position at lonza?
    Click the "Apply Now" button on this page. You will be redirected to lonza's official application portal hosted on workday where you can submit your application directly.
    When was the QC Associate, Analyst job at lonza posted?
    This QC Associate, Analyst position at lonza was posted on Sep 8, 2026. Apply as soon as possible — early applications are often reviewed first.
    QC Associate, Analyst
    lonza
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