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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
- Für die Lonza AG in Visp suchen wir eine/n Warehouse Operator/in 100%Tätigkeiten:Empfang, Lagerung und Verteilung von Materialien und ProduktenBestimmung der zu bewegenden Artikel anhand von Auftragsdokumenten wie Bestellungen und ProduktionsplänenDurchführung von Materialtransporten manuell, per Handhubwagen oder ElektrostaplerInspektion auf Schäden, Dokumentation der Materialbewegungen und SendungsverfolgungFür die Lonza AG in Visp suchen wir eine/n Warehouse Operator/in 100%Tätigkeiten:Empfang, Lagerung und Verteilung von Materialien und ProduktenBestimmung der zu bewegenden Artikel anhand von Auftragsdokumenten wie Bestellungen und ProduktionsplänenDurchführung von Materialtransporten manuell, per Handhubwagen oder ElektrostaplerInspektion auf Schäden, Dokumentation der Materialbewegungen und Sendungsverfolgung
- For Lonza AG in Visp, we are seeking a Scheduler 100% Key ResponsibilitiesEstablish and maintain the Operational Readiness Plan (ORP), ensuring strict alignment between Engineering (CAPEX) and OperationsManage integrated schedules in Primavera P6, ensuring logical connections and milestone alignment with the master CAPEX scheduleFacilitate planning workshops and perform resource loading to forecast workload for internal and external teamsMonitorFor Lonza AG in Visp, we are seeking a Scheduler 100% Key ResponsibilitiesEstablish and maintain the Operational Readiness Plan (ORP), ensuring strict alignment between Engineering (CAPEX) and OperationsManage integrated schedules in Primavera P6, ensuring logical connections and milestone alignment with the master CAPEX scheduleFacilitate planning workshops and perform resource loading to forecast workload for internal and external teamsMonitor
- Senior Bioprocess Engineer (Biologics)Location: Visp, Switzerland — 100% on-siteFunction: Operations / Manufacturing Science & Technology (MSAT)Type: Full-time, permanent (immediate start possible)The opportunityA fast-growing biologics site is expanding its Microbial / Mammalian / BioConjugates operations. We’re looking for an experienced Senior Bioprocess Engineer who can lead change on the shopfloor—owning operational readiness, documentation updates,Senior Bioprocess Engineer (Biologics)Location: Visp, Switzerland — 100% on-siteFunction: Operations / Manufacturing Science & Technology (MSAT)Type: Full-time, permanent (immediate start possible)The opportunityA fast-growing biologics site is expanding its Microbial / Mammalian / BioConjugates operations. We’re looking for an experienced Senior Bioprocess Engineer who can lead change on the shopfloor—owning operational readiness, documentation updates,
- 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 &
- 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,
