7 technologie Jobs in Visp, Wallis gefunden.

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

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 &

Für die Lonza AG in Visp suchen wir eine/n Automation Expert/in 100% Tätigkeiten: Projekte in der Automation (MES/DeltaV) operativ unterstützenSelbstständiges Testen und Dokumentieren von AutomationsprojektenSicherstellen der cGMP-gerechten Dokumentation im AnlageteamInformationsfluss innerhalb der Betriebsgruppe koordinierenGMP-Änderungswesen (Change Control) in den Systemen umsetzen

For our client, a global leader in the life sciences industry based in Visp, we are looking for a highly experienced CQV Engineer. The CQV Engineer is a critical role responsible for the commissioning, qualification, and validation of equipment and facilities. This role ensures that all installations meet stringent regulatory and technical standards, coordinating across departments to move projects from installation to full GMP compliance. General

Role OverviewWe are looking for an experienced Commissioning, Qualification & Validation (CQV) Engineer to support validation activities within a highly regulated pharmaceutical manufacturing environment.In this role, you will contribute to the commissioning, qualification, and validation of equipment, systems, and facilities, ensuring compliance with cGMP requirements and industry regulations.You will collaborate closely with engineering, quality, and

Senior Bioprocess Engineer (Biologics)Location: Visp, Switzerland — 100% on-siteFunction: Operations / Manufacturing Science & Technology (MSAT)Type: Full-time, permanent (immediate start possible)The opportunityA fast-growing biologics site is expanding its Microbial / Mammalian / BioConjugates operations. We’re looking for an experienced Senior Bioprocess Engineer who can lead change on the shopfloor—owning operational readiness, documentation updates,

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,