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- For our client, a global leader in the life sciences industry based in Visp, we are looking for a Piping Category Specialist and Buyer. The Piping Global Category Expert is a pivotal role responsible for managing procurement category activities for major investment projects. This role coordinates with Capex Lead Buyers and Piping Subject Matter Experts (SMEs) to plan and execute high-complexity projects, primarily at the Visp site, ensuring technicalFor our client, a global leader in the life sciences industry based in Visp, we are looking for a Piping Category Specialist and Buyer. The Piping Global Category Expert is a pivotal role responsible for managing procurement category activities for major investment projects. This role coordinates with Capex Lead Buyers and Piping Subject Matter Experts (SMEs) to plan and execute high-complexity projects, primarily at the Visp site, ensuring technical
- 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,
- Are you the person who actually enjoys the adrenaline of a surprise inspection? Do you find the "missing link" in a paper trail before anyone else even realizes it’s gone?Our client, a Randstad client, is looking for a Senior QMS & Compliance Expert to join their team in Visp. We need someone who treats Auditing as an art form, Compliance as a religion, and the Quality Management System (QMS) as their personal masterpiece.If you can stare down aAre you the person who actually enjoys the adrenaline of a surprise inspection? Do you find the "missing link" in a paper trail before anyone else even realizes it’s gone?Our client, a Randstad client, is looking for a Senior QMS & Compliance Expert to join their team in Visp. We need someone who treats Auditing as an art form, Compliance as a religion, and the Quality Management System (QMS) as their personal masterpiece.If you can stare down a
- Für die Lonza AG in Visp suchen wir ab sofort eine/n Bioprocess Engineer 100% (w/m/d) Deine KernaufgabenKampagnenleitung: Du verantwortest die Herstellung von Biokonjugaten unter cGMP-RichtlinienProzess-Support: Du sicherst die Chargenausführung, löst technische Probleme an den Anlagen und wertest Testergebnisse ausCompliance: Du übernimmst die lückenlose GMP-Dokumentation sowie das Erstellen von Kampagnenberichten und RisikoanalysenOptimierung:Für die Lonza AG in Visp suchen wir ab sofort eine/n Bioprocess Engineer 100% (w/m/d) Deine KernaufgabenKampagnenleitung: Du verantwortest die Herstellung von Biokonjugaten unter cGMP-RichtlinienProzess-Support: Du sicherst die Chargenausführung, löst technische Probleme an den Anlagen und wertest Testergebnisse ausCompliance: Du übernimmst die lückenlose GMP-Dokumentation sowie das Erstellen von Kampagnenberichten und RisikoanalysenOptimierung:
