For Lonza AG in Visp, we are seeking an QA Specialist 100% Responsibilities: Lead QA for projects and handle manufacturing/complaint inquiriesApprove recipes, protocols, transfer docs, and test plansManage Deviations, Change Controls, and CAPAsOversee risk assessments and regulatory gap analysisRepresent QA in inspections and cross-functional teamsSupport technology transfers and QMS improvements
For Lonza AG in Visp, we are seeking an QA Specialist 100% Responsibilities: Lead QA for projects and handle manufacturing/complaint inquiriesApprove recipes, protocols, transfer docs, and test plansManage Deviations, Change Controls, and CAPAsOversee risk assessments and regulatory gap analysisRepresent QA in inspections and cross-functional teamsSupport technology transfers and QMS improvements
Für die Lonza AG in Visp suchen wir eine/n Senior Qualifying Specialist/in 100% Tätigkeiten: Erstellung von Validierungsdokumenten wie URS, DQ, FMEA sowie FAT/SATDurchführung und Protokollierung von IQ/OQ/PQ für Equipment und UtilitiesDokumentation aller Ergebnisse im Rahmen des Quality Systems inklusive CAPA und Change ControlOptimierung des Validierungsprogramms unter Berücksichtigung aktueller regulatorischer ÄnderungenEnge Zusammenarbeit mit dem
Für die Lonza AG in Visp suchen wir eine/n Senior Qualifying Specialist/in 100% Tätigkeiten: Erstellung von Validierungsdokumenten wie URS, DQ, FMEA sowie FAT/SATDurchführung und Protokollierung von IQ/OQ/PQ für Equipment und UtilitiesDokumentation aller Ergebnisse im Rahmen des Quality Systems inklusive CAPA und Change ControlOptimierung des Validierungsprogramms unter Berücksichtigung aktueller regulatorischer ÄnderungenEnge Zusammenarbeit mit dem
Location: Switzerland (100% on-site)Contract type: Full-timeLanguage: German (mandatory); English a strong plusThe roleJoin a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.What you’ll doPlan and coordinate CQV for facilities &
Location: Switzerland (100% on-site)Contract type: Full-timeLanguage: German (mandatory); English a strong plusThe roleJoin a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.What you’ll doPlan and coordinate CQV for facilities &
For Lonza AG in Visp, we are seeking an Head Warehouse & Logistics 100% Responsibilities: Manage site logistics and secure Swissmedic licensing for growth projectsLead a team of 8 operators and 1 expert for aseptic filling operationsAct as Business Lead for local SAP-EWM implementationOversee cold chain, inventory, and material management (inbound/outbound)Represent the warehouse in regulatory inspections and customer auditsDrive operational takeover of
For Lonza AG in Visp, we are seeking an Head Warehouse & Logistics 100% Responsibilities: Manage site logistics and secure Swissmedic licensing for growth projectsLead a team of 8 operators and 1 expert for aseptic filling operationsAct as Business Lead for local SAP-EWM implementationOversee cold chain, inventory, and material management (inbound/outbound)Represent the warehouse in regulatory inspections and customer auditsDrive operational takeover of
For Lonza AG in Visp, we are seeking a Scheduler Site Supply Chain 100% Responsibilities Create and update short-term schedules to drive operational executionOptimize production sequences for maximum resource and facility utilizationAlign with Procurement and Production to ensure realistic planning constraintsManage system parameters, BOMs, and routings to support the MRP processTrack KPIs and production data to identify trends and process improvements
For Lonza AG in Visp, we are seeking a Scheduler Site Supply Chain 100% Responsibilities Create and update short-term schedules to drive operational executionOptimize production sequences for maximum resource and facility utilizationAlign with Procurement and Production to ensure realistic planning constraintsManage system parameters, BOMs, and routings to support the MRP processTrack KPIs and production data to identify trends and process improvements
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