For one of our clients, a world leader in the CDMO industry and biotechnology, we are currently looking for a Bioprocess Engineer.General Information:Start date: 01.02.2026Duration: until 30.11.2026Workplace: VispWorkload: 100%Working hours: StandardOur client’s site in Visp, Switzerland is growing and for their Biologics organization, we are seeking experienced Bioprocess Engineers.Tasks & Responsibilities:Correct execution of production campaigns in
For one of our clients, a world leader in the CDMO industry and biotechnology, we are currently looking for a Bioprocess Engineer.General Information:Start date: 01.02.2026Duration: until 30.11.2026Workplace: VispWorkload: 100%Working hours: StandardOur client’s site in Visp, Switzerland is growing and for their Biologics organization, we are seeking experienced Bioprocess Engineers.Tasks & Responsibilities:Correct execution of production campaigns in
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,
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 &
QA CSV SpecialistFor our Client in Visp we are searching for a Computer System Validation Specialist/Engineer (CSV) to carry out a variety of tasks related to the validation and lifecycle management of computerized systemsKey Responsibilities:Identify or create industry best practices and implement these within the framework of existing GAMP regulations. Strategic implementation of CSV process improvements and tactical support of CSV operations to meet
QA CSV SpecialistFor our Client in Visp we are searching for a Computer System Validation Specialist/Engineer (CSV) to carry out a variety of tasks related to the validation and lifecycle management of computerized systemsKey Responsibilities:Identify or create industry best practices and implement these within the framework of existing GAMP regulations. Strategic implementation of CSV process improvements and tactical support of CSV operations to meet
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
Für unseren Kunden Lonza AG am Standort Visp suchen wir einen erfahrenen Elektroinstallateur (m/w/d) zur Verstärkung des Teams.Ihre Aufgaben:Installation, Inbetriebnahme und Instandhaltung von Elektro-, Mess- und Regelanlagen (EMR)Zusammenarbeit mit Installationsteams bei der Errichtung und Wartung von EMR-AnlagenSelbstständige Durchführung von Tests und Inbetriebnahmen von EMR-AnlagenEigenständige Behebung von Störungen an EMR-Anlagen
Für unseren Kunden Lonza AG am Standort Visp suchen wir einen erfahrenen Elektroinstallateur (m/w/d) zur Verstärkung des Teams.Ihre Aufgaben:Installation, Inbetriebnahme und Instandhaltung von Elektro-, Mess- und Regelanlagen (EMR)Zusammenarbeit mit Installationsteams bei der Errichtung und Wartung von EMR-AnlagenSelbstständige Durchführung von Tests und Inbetriebnahmen von EMR-AnlagenEigenständige Behebung von Störungen an EMR-Anlagen
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