CQV Engineer / Qualification & Validation Engineer

Develop and maintain commissioning and qualification documents for new plants, including PQs for critical systems and ongoing SLC support post-implementation. Supervise and resolve deviations, manage changes (GEP and GMP), and implement CAPAs effectively. Coordinate efforts between internal teams and external service providers and suppliers to ensure seamless project execution. Present qualification documents during audits and inspections, showcasing the outstanding standards maintained.

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.

• Graduate from a technical school (HF) / university of applied sciences (FH) or hold a university degree

• Proven experience in a regulated GMP environment, specifically in commissioning, qualification, and validation of systems like refrigerators, freezers, clean media, and process engineering equipment

• Strong proficiency in MS Office; familiarity with COMOS, DMS, Kneat, TrackWise, and SAP is advantageous

• Proficient in both written and spoken German and/or English

• Demonstrate independent, flexible work habits, with excellent communication skills and a structured, focused approach to tasks

• Open to new ideas, agile in thinking, and proactive in problem-solving.