Competitive salary with numerous lifestyle, family, and leisure benefits.
What you will do: Act as QA Representative for assigned projects, ensuring Quality oversight of raw materials, packaging materials, single-use systems, filters, and other GMP-relevant materials used in manufacturing operations. Support material qualification activities, including QA Approval of risk assessments, specification reviews, and QC documentation. Prepare, review, and approve material risk assessments and product statements. Ensure suppliers are appropriately qualified for the intended use of materials. Assess, review and approve material-related quality records, investigations, deviations, CAPAs, and change requests. Act as the Quality representative in cross-functional teams, collaborating with Operations, MSAT, Supply Chain, Procurement, Regulatory Affairs, and Quality Control. Ensure all QA activities are performed in compliance with applicable SOPs, internal standards, and regulatory expectations. Support health authority inspections, customer audits, and internal audits by providing subject matter expertise in material management.
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.
