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
Commissioning Qualification Validation Engineer For our Client in Visp we are searching for a Commissioning Qualification Validation Engineer (CQV) to carry out a variety of tasks related to the validation of equipment and facilities.Key Responsibilities:CQV validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis and Risk Assessment.Coordination of the
Commissioning Qualification Validation Engineer For our Client in Visp we are searching for a Commissioning Qualification Validation Engineer (CQV) to carry out a variety of tasks related to the validation of equipment and facilities.Key Responsibilities:CQV validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis and Risk Assessment.Coordination of the
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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