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.
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.
