Für die Lonza AG in Visp suchen wir ab sofort einen Scheduler 100% (m/w/d). Key ResponsibilitiesE2E Scheduling: Own and manage end-to-end program schedules for Operational ReadinessWorkload Management: Update and track resource workload for PCP manufacturing buildingsStakeholder Lead: Lead meetings with internal teams (QA, QC, Ops, MSAT, Plant Eng.) for schedule updates and trackingProject Support: Support general planning tasks beyond core scheduling to
Für die Lonza AG in Visp suchen wir ab sofort einen Scheduler 100% (m/w/d). Key ResponsibilitiesE2E Scheduling: Own and manage end-to-end program schedules for Operational ReadinessWorkload Management: Update and track resource workload for PCP manufacturing buildingsStakeholder Lead: Lead meetings with internal teams (QA, QC, Ops, MSAT, Plant Eng.) for schedule updates and trackingProject Support: Support general planning tasks beyond core scheduling to
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:
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 technical
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 technical
Senior SAP Basis Engineer (Remote)We are seeking an experienced and proactive Senior SAP Basis Engineer to join a global IT team supporting complex SAP landscapes. In this role, you will be responsible for the administration, optimization, and reliability of SAP systems, ensuring high performance, security, and alignment with business objectives.This is a fully remote position, ideal for someone who thrives in an autonomous work environment while
Senior SAP Basis Engineer (Remote)We are seeking an experienced and proactive Senior SAP Basis Engineer to join a global IT team supporting complex SAP landscapes. In this role, you will be responsible for the administration, optimization, and reliability of SAP systems, ensuring high performance, security, and alignment with business objectives.This is a fully remote position, ideal for someone who thrives in an autonomous work environment while
Anstellungsart: Festanstellung bei einem Kunden von RandstadArbeitsort: Visp (100% vor Ort)Arbeitszeit: Wöchentlich wechselndes 3-Schicht-Modell (Montag – Freitag, keine Wochenendarbeit)Ihre Aufgaben:Anlagenbedienung: Überwachung und Bedienung der Abfüllanlage für flüssige pharmazeutische Produkte unter Einhaltung höchster Qualitätsstandards.Isolator-Tätigkeiten: Durchführung spezialisierter Aufgaben am Isolator im Rahmen der sterilen Abfüllung.Logistik &
Anstellungsart: Festanstellung bei einem Kunden von RandstadArbeitsort: Visp (100% vor Ort)Arbeitszeit: Wöchentlich wechselndes 3-Schicht-Modell (Montag – Freitag, keine Wochenendarbeit)Ihre Aufgaben:Anlagenbedienung: Überwachung und Bedienung der Abfüllanlage für flüssige pharmazeutische Produkte unter Einhaltung höchster Qualitätsstandards.Isolator-Tätigkeiten: Durchführung spezialisierter Aufgaben am Isolator im Rahmen der sterilen Abfüllung.Logistik &
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,
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