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- Für die Lonza AG am Standort Visp suchen wir per sofort ein/e Reinigungskraft 80- 100%. Die Arbeitszeiten sind von Montag bis Freitag.Deine Aufgaben:Reinraumreinigung: Decken, Wände, Fenster, Boden, Einrichtungen und Anlagen in den verschiedenen Betrieben reinigenBewirtschaften von Hygiene und BekleidungsartikelReinigungsaufträge über MODA-System abwickelnFür die Lonza AG am Standort Visp suchen wir per sofort ein/e Reinigungskraft 80- 100%. Die Arbeitszeiten sind von Montag bis Freitag.Deine Aufgaben:Reinraumreinigung: Decken, Wände, Fenster, Boden, Einrichtungen und Anlagen in den verschiedenen Betrieben reinigenBewirtschaften von Hygiene und BekleidungsartikelReinigungsaufträge über MODA-System abwickeln
- 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,
