For one of our clients, an international pharmaceutical company, we are seeking a Computer System Validation Engineer.General Information:Start date: 01.05.2026End Date: 31.10.2026Workplace: Schachen, LuzernHome office: No, 100% onsite, 5 days per week (home office is available on a need basis and in coordination with lab heads and managers)Workload: 100%Working hours: StandardAbout the work:Our client’s Metrology and Validation department in Analytical
For one of our clients, an international pharmaceutical company, we are seeking a Qualification and Cleaning/Sterilization Validation Subject Matter Expert.General Information:Start date: 01.07.2026End Date: 30.11.2027Workplace: Schachen, LuzernHome office: No, 100% onsiteWorkload: 100%Working hours: StandardAbout the work:The Qualification and Cleaning/Sterilization Validation Subject Matter Expert (SME) is a role within the Technology Lifecycle
For one of our clients, an international pharmaceutical company, we are seeking a GMP Documentation Specialist.General Information:Start date: 01.07.2026End Date: 30.06.2027Workplace: Schachen, LuzernHome office: No, 100% onsiteWorkload: 100%Working hours: StandardAbout the work:The GMP Documentation Specialist supports clinical biologics manufacturing by performing operational review of executed batch records and ensuring documentation supports ALCOA+
6. May 2026
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