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- 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 demFür 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
- 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 improvementsFor 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
- 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,
