Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of .
Key Responsibilities:
Execute and document validation activities (IQ, OQ, PQ, PPQ), including risk assessments and periodic reviews.
Support the full Validation Life Cycle—from design through revalidation and continuous improvement.
Collaborate with internal and external teams to ensure new systems meet cGMP and validation requirements.
Maintain and update validation-related documentation (SOPs, Change Controls, CAPAs, Deviations).
Assist in investigations and resolution of deviations involving equipment, systems, and processes.
Provide validation support during audits and ensure inspection readiness
Key Qualifications:
Bachelor’s degree in engineering, life sciences, or related field
2–5 years of validation experience in a GMP-regulated environment.
Cross- Functional Communication
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.