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- For Lonza AG in Visp, we are seeking an Production Operator 100%Key Responsibilities:Perform various tasks in production functionsIdentify and fix process deviationsExecute steps, record data and handle calculationsAssist in training new team membersFor Lonza AG in Visp, we are seeking an Production Operator 100%Key Responsibilities:Perform various tasks in production functionsIdentify and fix process deviationsExecute steps, record data and handle calculationsAssist in training new team members
- Für die Arxada AG in Visp suchen wir eine/n Operator/in im 4-Schicht-Betrieb 100% Tätigkeiten: Sichere und termingerechte Durchführung von unterschiedlichen Arbeiten an den ProduktionsanlagenFlexible Arbeit in den zugewiesenen Anlagen vor Ort und Unterstützung bei Umstellungs- und RevisionsarbeitenSelbstständiges Arbeiten unter Einhaltung der Sicherheitsvorschriften (SiVo)Für die Arxada AG in Visp suchen wir eine/n Operator/in im 4-Schicht-Betrieb 100% Tätigkeiten: Sichere und termingerechte Durchführung von unterschiedlichen Arbeiten an den ProduktionsanlagenFlexible Arbeit in den zugewiesenen Anlagen vor Ort und Unterstützung bei Umstellungs- und RevisionsarbeitenSelbstständiges Arbeiten unter Einhaltung der Sicherheitsvorschriften (SiVo)
- For Lonza AG in Visp, we are seeking a Scheduler Site Supply Chain 100% Responsibilities Create and update short-term schedules to drive operational executionOptimize production sequences for maximum resource and facility utilizationAlign with Procurement and Production to ensure realistic planning constraintsManage system parameters, BOMs, and routings to support the MRP processTrack KPIs and production data to identify trends and process improvementsFor Lonza AG in Visp, we are seeking a Scheduler Site Supply Chain 100% Responsibilities Create and update short-term schedules to drive operational executionOptimize production sequences for maximum resource and facility utilizationAlign with Procurement and Production to ensure realistic planning constraintsManage system parameters, BOMs, and routings to support the MRP processTrack KPIs and production data to identify trends and process improvements
- 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,
- 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 &
