Find Lonza jobs in Netherlands, Switzerland and United Kingdom.
You lead the site Quality organization and serve as the key authority for GMP compliance and quality strategy. In this executive leadership role, you shape the site’s quality culture while enabling the successful delivery of innovative therapies,
Play a pivotal role in advancing next-generation purification technologies. This is a hands-on scientific role where you will drive innovation in downstream processing and contribute to the development of intensified, scalable purification solutions for
In this role, you will oversee complex analytical projects, drive method development and validation activities, and ensure the highest standards of data integrity and regulatory compliance. You will collaborate closely with cross-functional partners -
You will deliver technical solutions to accelerate the development of purification processes for complex biotherapeutic treatments, helping maintain Lonza’s position as a leading global CDMO. Organize, curate, and analyze large datasets from primary
Assess, review and approve quality records and release files/dossiers e.g. deviations, change control, CAPAs, investigations, effectiveness checks, extensions, complaints, APR/PQRs, in line with current local SOPs. Act as QA contact for specific projects