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- 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 meetQA 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
- 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,
- 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,
- 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 customerFor 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
- Für die Lonza AG in Visp suchen wir eine/n Laborant/in Qualitätskontrolle 100%Tätigkeiten:Durchführung täglicher QC-Aktivitäten unter GMP- und SicherheitsstandardsProbenmanagement (Annahme, Lagerung, Dokumentation, Entsorgung)Routinewartung und Kalibrierung von LaborgeräteLabororganisation (Materialversorgung, Lagerbestände, Housekeeping)Unterstützung bei Materialfreigaben und ProbenversandFür die Lonza AG in Visp suchen wir eine/n Laborant/in Qualitätskontrolle 100%Tätigkeiten:Durchführung täglicher QC-Aktivitäten unter GMP- und SicherheitsstandardsProbenmanagement (Annahme, Lagerung, Dokumentation, Entsorgung)Routinewartung und Kalibrierung von LaborgeräteLabororganisation (Materialversorgung, Lagerbestände, Housekeeping)Unterstützung bei Materialfreigaben und Probenversand
- Für die Lonza AG in Visp suchen wir eine/n Laborant/in in QC Mikrobiologie Analytik 100%Tätigkeiten:Keimidentifizierungen (mittels PCR und Massenspektrometrie) und Endotoxin MessungenEigenständige Durchführung, Auswertung und Berichterstattung von AnalysenGMP-konforme Dokumentation aller LabortätigkeitenDurchführung von MethodenverifizierungenFür die Lonza AG in Visp suchen wir eine/n Laborant/in in QC Mikrobiologie Analytik 100%Tätigkeiten:Keimidentifizierungen (mittels PCR und Massenspektrometrie) und Endotoxin MessungenEigenständige Durchführung, Auswertung und Berichterstattung von AnalysenGMP-konforme Dokumentation aller LabortätigkeitenDurchführung von Methodenverifizierungen
