Compensation programs that recognize high performance
What you will do: Responsible for Equipment, QC, Computerized System Validation (CSV) and Automation deliverables for new aseptic facilities, equipment and utilities related to the GMP manufacturing of drug products Representing Quality in the CAPEX project organization in regards to Equipment, QC, Computerized System Validation (CSV) and Automation Reviewing and releasing quality related to Equipment, QC, Computerized System Validation (CSV) and Automation project deliverables Ensuring Equipment, QC, Computerized System Validation (CSV) and Automation deliverables meet Global procedures, regulatory requirements and policies Being a Subject Matter Expert (SME) and providing guidance and recommendations to internal and external project stakeholders
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.
