For Lonza AG in Visp, we are seeking a Scheduler 100% Key ResponsibilitiesEstablish and maintain the Operational Readiness Plan (ORP), ensuring strict alignment between Engineering (CAPEX) and OperationsManage integrated schedules in Primavera P6, ensuring logical connections and milestone alignment with the master CAPEX scheduleFacilitate planning workshops and perform resource loading to forecast workload for internal and external teamsMonitor
For Lonza AG in Visp, we are seeking a Scheduler 100% Key ResponsibilitiesEstablish and maintain the Operational Readiness Plan (ORP), ensuring strict alignment between Engineering (CAPEX) and OperationsManage integrated schedules in Primavera P6, ensuring logical connections and milestone alignment with the master CAPEX scheduleFacilitate planning workshops and perform resource loading to forecast workload for internal and external teamsMonitor
About the RoleFor one of our clients, we are looking for an experienced Project Engineer to support the planning, execution, and optimization of technical investment projects within a production environment.In this role, you will develop technical concepts, advise internal stakeholders on decision-making, manage detailed engineering activities, secure project funding, and oversee execution. You will be fully accountable for costs, timelines, and
About the RoleFor one of our clients, we are looking for an experienced Project Engineer to support the planning, execution, and optimization of technical investment projects within a production environment.In this role, you will develop technical concepts, advise internal stakeholders on decision-making, manage detailed engineering activities, secure project funding, and oversee execution. You will be fully accountable for costs, timelines, and
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,
Für unseren Kunden, ein internationales Unternehmen in Visp, suchen wir per sofort einen engagierten Betriebs-/Anlagemeister (m/w/d).Als Betriebs-/Anlagemeister (m/w/d) bist Du zuständig für die technische und logistische Abwicklung von Produktionskampagnen in unserem Betrieb zur Herstellung von Biokonjugaten.Du bist Mitglied eines interdisziplinären Teams und arbeitest aktiv in Projektteams mit, die sich um Investitionen sowie die Optimierung von
Für unseren Kunden, ein internationales Unternehmen in Visp, suchen wir per sofort einen engagierten Betriebs-/Anlagemeister (m/w/d).Als Betriebs-/Anlagemeister (m/w/d) bist Du zuständig für die technische und logistische Abwicklung von Produktionskampagnen in unserem Betrieb zur Herstellung von Biokonjugaten.Du bist Mitglied eines interdisziplinären Teams und arbeitest aktiv in Projektteams mit, die sich um Investitionen sowie die Optimierung von
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 &
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