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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,
- Tu aimes produire de la bière, tu aimes prendre des responsabilités et tu es prêt à travailler dans une brasserie ? Chez notre client Feldschlösschen, le poste temporaire suivant est disponible à la nouvelle Brasserie Valaisanne à Vétroz: Brasseur Opérateur 100%Voici tes tâches principales: Utilisation, surveillance et entretien de l'installation de productionRespect des règles de qualité, d'hygiène et de sécuritéMise en ?uvre du système de gestion de laTu aimes produire de la bière, tu aimes prendre des responsabilités et tu es prêt à travailler dans une brasserie ? Chez notre client Feldschlösschen, le poste temporaire suivant est disponible à la nouvelle Brasserie Valaisanne à Vétroz: Brasseur Opérateur 100%Voici tes tâches principales: Utilisation, surveillance et entretien de l'installation de productionRespect des règles de qualité, d'hygiène et de sécuritéMise en ?uvre du système de gestion de la
- 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,
- Title: Quality SpecialistLocation: Visp, Valais, Switzerland (On-site)We are looking for a Quality Specialist with experience in deviation investigations and CAPA management within a GMP-regulated environment – ideally with strong knowledge of processes related to monoclonal antibodies.This role is critical to ensuring regulatory compliance, preventing recurring issues, and strengthening the quality system through effective corrective and preventiveTitle: Quality SpecialistLocation: Visp, Valais, Switzerland (On-site)We are looking for a Quality Specialist with experience in deviation investigations and CAPA management within a GMP-regulated environment – ideally with strong knowledge of processes related to monoclonal antibodies.This role is critical to ensuring regulatory compliance, preventing recurring issues, and strengthening the quality system through effective corrective and preventive
- 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 &
- 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, andRole 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
