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Lonza in Stein, AG, Switzerland is seeking a dedicated specialist to lead aseptic compounding processes, provide hands-on operator support, and drive deviations and investigations. You will execute and support validation activities, maintain GMP documentation, and keep facilities inspection-ready in a sterile manufacturing setting.
The role requires a BSc/MSc in Life Sciences, strong GMP experience, fluent English, and conversational German (B1).
The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
Join a collaborative, proactive and diverse team where you will drive process excellence across compounding operations, support operators with technical expertise, lead deviations, investigations, and execute validation and qualification activities while ensuring continuous inspection readiness.
As part of an exciting greenfield growth project, you will take ownership, make a visible impact, and contribute to the successful delivery of safe, high-quality products.
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, 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.