Für die Lonza AG in Visp suchen wir eine/n QC Operator/in 4 Schicht.Tätigkeiten:Probensammlung im Umwelt- und VersorgungsbereichGMP-konforme DokumentationUmweltmonitoring in klassifizierten Bereichen (Luft, Oberflächen, Versorgungssysteme)Probenahme gemäss SOPs und GMP-RichtlinienTeamzusammenarbeit zur Sicherstellung der Probenahmepläne
Für die Lonza AG in Visp suchen wir eine/n QC Operator/in 4 Schicht.Tätigkeiten:Probensammlung im Umwelt- und VersorgungsbereichGMP-konforme DokumentationUmweltmonitoring in klassifizierten Bereichen (Luft, Oberflächen, Versorgungssysteme)Probenahme gemäss SOPs und GMP-RichtlinienTeamzusammenarbeit zur Sicherstellung der Probenahmepläne
"Die Arbeit, die du heute machst, könnte morgen Leben retten."Für die Firma Jabil Manufacturing GmbH (ex Depuy-Synthes) am Standort Raron suchen wir CNC Maschinenbediener (m/w) für einen temporären Einsatz.Diese spannenden Aufgaben warten auf dich:Bereitstellen von Werkzeugen, Kontrollmitteln und Vorrichtungen gemäss Anweisung oder UnterlagenBedienen und Überwachen sowie teilweise Einrichten von MaschinenReinigen von Maschinen und Ausführen von
"Die Arbeit, die du heute machst, könnte morgen Leben retten."Für die Firma Jabil Manufacturing GmbH (ex Depuy-Synthes) am Standort Raron suchen wir CNC Maschinenbediener (m/w) für einen temporären Einsatz.Diese spannenden Aufgaben warten auf dich:Bereitstellen von Werkzeugen, Kontrollmitteln und Vorrichtungen gemäss Anweisung oder UnterlagenBedienen und Überwachen sowie teilweise Einrichten von MaschinenReinigen von Maschinen und Ausführen von
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 teamsMonitor
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 teamsMonitor
QA CSV SpecialistFor our Client in Visp we are searching for a Computer System Validation Specialist/Engineer (CSV) to carry out a variety of tasks related to the validation and lifecycle management of computerized systemsKey Responsibilities:Identify or create industry best practices and implement these within the framework of existing GAMP regulations. Strategic implementation of CSV process improvements and tactical support of CSV operations to meet
QA CSV SpecialistFor our Client in Visp we are searching for a Computer System Validation Specialist/Engineer (CSV) to carry out a variety of tasks related to the validation and lifecycle management of computerized systemsKey Responsibilities:Identify or create industry best practices and implement these within the framework of existing GAMP regulations. Strategic implementation of CSV process improvements and tactical support of CSV operations to meet
For one of our clients, a world leader in the CDMO industry and biotechnology, we are currently looking for a Bioprocess Engineer.General Information:Start date: 01.02.2026Duration: until 30.11.2026Workplace: VispWorkload: 100%Working hours: StandardOur client’s site in Visp, Switzerland is growing and for their Biologics organization, we are seeking experienced Bioprocess Engineers.Tasks & Responsibilities:Correct execution of production campaigns in
For one of our clients, a world leader in the CDMO industry and biotechnology, we are currently looking for a Bioprocess Engineer.General Information:Start date: 01.02.2026Duration: until 30.11.2026Workplace: VispWorkload: 100%Working hours: StandardOur client’s site in Visp, Switzerland is growing and for their Biologics organization, we are seeking experienced Bioprocess Engineers.Tasks & Responsibilities:Correct execution of production campaigns in
For one of our clients, a world leader in the CDMO industry and biotechnology, we are currently looking for a Scientist - QC Microbiology Lead.General Information:Start date: 01.12.2025Duration: until 31.08.2026Workplace: VispWorkload: 100%Remote/Home Office: possible, max 2 days, 100 % on-site preferredWorking hours: StandardTasks & Responsibilities:Technical representation of the QC Microbiology department internally and at customer
For one of our clients, a world leader in the CDMO industry and biotechnology, we are currently looking for a Scientist - QC Microbiology Lead.General Information:Start date: 01.12.2025Duration: until 31.08.2026Workplace: VispWorkload: 100%Remote/Home Office: possible, max 2 days, 100 % on-site preferredWorking hours: StandardTasks & Responsibilities:Technical representation of the QC Microbiology department internally and at customer
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,
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