9 Temporary jobs found in Schachen, Luzern

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 Excellenc

For one of our clients, a global pharmaceutical company, we are looking for a Laboratory Technician Scientist in a QC Bioanalytical Lab.General Information:Start date: 01.05.2026End date: 30.04.2027Workplace: Schachen, LucerneWorkload: 100%Working Hours: StandardHome Office: Not possible, 100% on-siteAbout the job:The integrated Biologics Analytical Department provides support to the Biotechnology Department by performing release and stability testing of b

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 R&

For one of our clients, an international pharmaceutical company, we are seeking a Senior Production Operator.General Information:Start date: 01.06.2026End Date: 31.05.2027Workplace: Schachen, LuzernHome office: No, 100% onsiteWorkload: 100%Working hours: StandardAbout the work:You will be part of the Biologics Manufacturing Science and Operations department, in particular Drug Substance Bioprocess.Tasks & Responsibilities:Support cross-functional team in r

For one of our clients, an international pharmaceutical company, we are seeking an Operator for Biotech Support Operations.General Information: Start date: ASAP (high urgency)End Date: 1 yearWorkplace: Schachen, LuzernHome office: No, 100% onsiteWorkload: 100%Working hours: Standard Tasks & Responsibilities: Perform routine operator activities within the Weigh & Dispense (W&D) and Solution Supply Areas, in strict adherence to GMP and GDocP requirementsPerf

Für einen unserer Kunden, ein internationales pharmazeutisches Unternehmen, suchen wir eine/n Clinical Packaging Technician/Operator.Allgemeine Informationen:Startdatum: 18.05.2026Enddatum: 17.05.2028Arbeitsort: Schachen, LuzernHomeoffice: Nein, 100% vor Ort (Onsite)Arbeitspensum: 100%Arbeitszeiten: StandardÜber die Tätigkeit:Die Organisation Global Clinical Supply (GCS) ist für das End-to-End-Management klinischer Studien verantwortlich. GCS überwacht die

On behalf of our Client, an international pharma company based in canton Lucerne, we are looking for a dedicated and organized Logistics Specialist who enjoys international logistics, dealing with compliance issues and collaborating with internal and external partners.General Information: Start date: ASAPDuration: 2 yearsExtension: possible, to be discussedContract: temporary contract via RandstadLocation: Schachen (LU)Workload: 100%Home office: not possib

For one of our clients, a global pharmaceutical company in Schachen, we are looking for a Lab Technician Scientist in a QC Bioanalytical Lab to join their Biologics Analytical Department. The integrated Biologics Analytical Department provides support to the Biotechnology Department by performing release and stability testing of biological drug substances and is supporting global outsourcing of analytics for biologics, followed by study and quality monitor

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+ sta