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- 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,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,
- Für die Lonza AG in Visp suchen wir eine/n QC Operator/in 4 Schicht.Tätigkeiten:Probensammlung im Umwelt- und VersorgungsbereichGMP-konforme DokumentationUmweltmonitoring in klassifizierten Bereichen (Luft, Oberflächen, Versorgungssysteme)Probenahme gemäss SOPs und GMP-RichtlinienTeamzusammenarbeit zur Sicherstellung der ProbenahmepläneFür die Lonza AG in Visp suchen wir eine/n QC Operator/in 4 Schicht.Tätigkeiten:Probensammlung im Umwelt- und VersorgungsbereichGMP-konforme DokumentationUmweltmonitoring in klassifizierten Bereichen (Luft, Oberflächen, Versorgungssysteme)Probenahme gemäss SOPs und GMP-RichtlinienTeamzusammenarbeit zur Sicherstellung der Probenahmepläne
- 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,
