Compensation programs that recognize high performance; benefits vary by role and location.
What you will do: Validation of new analytical Biochemistry methods (ELISA, qPCR, Biacore) Creation and release of technical documentation, creation of verification plans and reports Collection, investigation and evaluation of verification data, weak points as well as implementation and monitoring of corrective measures Coordinate the routine Quality Control analytics with Lab Technicians and manage GMP deviations and OOS/OOE results as needed You are in contact with various Lonza internal stakeholders (e.g. Quality Control, Quality Assurance, Project Leaders)
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.
