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- 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
- 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,
- We are seeking an experienced and proactive Senior SAP Basis Engineer to join our team. In this role, you will be responsible for ensuring the performance, stability, and security of complex SAP landscapes. You will work closely with cross-functional teams to support strategic initiatives, system enhancements, and continuous improvements that align IT capabilities with business goals.This is a fully remote position, ideal for someone who thrives in anWe are seeking an experienced and proactive Senior SAP Basis Engineer to join our team. In this role, you will be responsible for ensuring the performance, stability, and security of complex SAP landscapes. You will work closely with cross-functional teams to support strategic initiatives, system enhancements, and continuous improvements that align IT capabilities with business goals.This is a fully remote position, ideal for someone who thrives in an
- 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
- Vous êtes passionné·e par la chimie analytique ?Nous recherchons un·e technicien·ne de laboratoire maîtrisant l’HPLC et la GC.2 postes à pourvoirBasé à MartignyTemporaire : 6 mois - remplacement congé maternité Vos missionsRéaliser les analyses chimiques liées au développement et à l’optimisation de procédés de fabrication de principes actifs.Participer aux validations et transferts analytiques dans le respect des GMP.Contribuer aux investigationsVous êtes passionné·e par la chimie analytique ?Nous recherchons un·e technicien·ne de laboratoire maîtrisant l’HPLC et la GC.2 postes à pourvoirBasé à MartignyTemporaire : 6 mois - remplacement congé maternité Vos missionsRéaliser les analyses chimiques liées au développement et à l’optimisation de procédés de fabrication de principes actifs.Participer aux validations et transferts analytiques dans le respect des GMP.Contribuer aux investigations
