For one of our clients, an international pharmaceutical company based in canton Lucerne, we are seeking a Biotech Production Operator.General Information: Start date: ASAPDuration: 1 yearExtension: possibleContract type: temporary contract via Randstad (employment)Workplace: Schachen, LucerneHome office: not possible, 100% onsiteWorkload: 100% Tasks & Responsibilities: Perform routine operator activities within the Weigh & Dispense (W&D) and Solution
For one of our clients, an international pharmaceutical company based in canton Lucerne, we are seeking a Production Operator.In this role you will join the Biologics Manufacturing Science and Operations department and support Drug Substance Bioprocess.General Information: Start date: ASAPDuration: 1 yearExtension: possibleContract type: temporary contract via Randstad (employment)Workplace: Schachen, LucerneHome office: not possible, 100%
For one of our clients, an international pharmaceutical company, we are seeking a Documentation Specialist.General Information:Start date: 13.10.2026End Date: 12.04.2027Workplace: Schachen, LuzernWorkload: 100%Working hours: StandardHome Office: primarily onsite, home office is available on a need basisAbout the work:Our client’s Pharmaceutical Analysis & Digital Technologies (PADT) department located in Schachen in Switzerland, is currently offering an
For one of our clients, an international pharmaceutical company based in canton Lucerne, we are seeking a Senior Specialist, Strategy and Operational Excellence.General Information: Start date: ASAP / to be discussedDuration: 1 yearExtension: to be discussedContract type: temporary contract via Randstad (employment)Workplace: Schachen, LucerneHome office: not possibleWorkload: 100%Purpose of the role:The Strategy & Operational Excellence Team is tasked to
For one of our clients, an international pharmaceutical company, we are seeking an Associate Process Specialist - Downstream Operations.General Information:Start date: 01.10.2026Duration: 12 monthsWorkplace: Schachen, LuzernHome office: not possible, 100% onsiteWorkload: 100%Working hours: StandardAbout the work:As a member of the manufacturing team, you will be responsible for supporting various activities related to the implementation and GMP