Support analytical development for Mammalian products at Lonza Visp through hands-on laboratory work and process improvement projects.

Join Lonza's Quality Control team in Basel to drive laboratory compliance and support biopharmaceutical manufacturing.

Be responsible for the supervision, support and life cycle management of bioconjugate processes at Lonza's Visp site.

This site-based role in Visp focuses on implementing and supporting MES and DeltaV systems for biopharmaceutical manufacturing.

Praktikum in Visp mit Fokus auf Operational Excellence und kontinuierliche Verbesserung in der Produktion von Small Molecules.

Drive supplier qualification and compliance activities for GMP-relevant materials, services, and equipment at Lonza's Drug Product Services in Stein, Switzerland.

Lead GMP deviation investigations and drive continuous improvement in biopharmaceutical manufacturing at Lonza in Visp.

Lead and coordinate complex inspections and customer audits across two sites in Switzerland to ensure continuous audit readiness in a dynamic pharmaceutical environment.

Sie sorgen für die GMP-konforme Versorgung der Produktion mit Materialien und unterstützen die Herstellung hochwertiger Arzneimittel.

Lead quality and compliance improvements in QC at Lonza in Visp, supporting regulatory readiness and laboratory excellence.