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- For Lonza AG in Visp, we are seeking an Production Operator 100%Key Responsibilities:Perform various tasks in production functionsIdentify and fix process deviationsExecute steps, record data and handle calculationsAssist in training new team membersFor Lonza AG in Visp, we are seeking an Production Operator 100%Key Responsibilities:Perform various tasks in production functionsIdentify and fix process deviationsExecute steps, record data and handle calculationsAssist in training new team members
- 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 improvementsFor 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
- About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,
