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Lonza Group AG in Visp, Switzerland, is seeking a QA professional to drive quality assurance and regulatory compliance on the production floor. The role emphasizes active participation in tech transfer, deviations review, and risk-based decision making to uphold cGMP standards.
The ideal candidate has a Life Sciences background, hands-on QA experience in pharma, and fluency in English. This site-based position offers close collaboration across Manufacturing, Engineering and Quality Control to
Are you looking to make a meaningful impact on cutting-edge pharmaceutical manufacturing? Join our dynamic team in Visp to champion quality excellence, tech transfer, and operational compliance in our state-of-the-art facility.
This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
At Lonza, their people are their greatest strength. With 30+ sites across five continents, their globally connected teams work together every day to manufacture the medicines of tomorrow. Their core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who they are and how they work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work they want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, they value diversity and are committed to creating an inclusive environment.