Competitive local benefits.
What you will do: You collect, evaluate, and summarize monitoring data using MODA, LIMS, and digital analysis tools. You document GMP‑relevant activities and lead investigations of alert or action level excursions. You drive root‑cause investigations and align corrective actions with key stakeholders. You create, review, and approve DMS documents to ensure accuracy and compliance. You improve monitoring processes to enhance data quality, efficiency, and robustness. You implement monitoring updates and manage MODA‑related changes under change control. You represent the team during inspections, audits, and customer visits with confidence.
About LonzaAt 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.
