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- 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,
- Ingénieur·e Civil – Aménagement & Renaturation de Cours d’EauSuisse | SionJe recherche pour l’un de mes clients – un bureau d’ingénierie reconnu à l'internationnal et en pleine expansion en Suisse Romande – un·e Ingénieur·e Civil spécialisé·e dans l’aménagement et la renaturation de cours d’eau.Si vous souhaitez mettre vos compétences au service de projets à forte valeur environnementale, tout en évoluant dans une équipe dynamique et engagée, cetteIngénieur·e Civil – Aménagement & Renaturation de Cours d’EauSuisse | SionJe recherche pour l’un de mes clients – un bureau d’ingénierie reconnu à l'internationnal et en pleine expansion en Suisse Romande – un·e Ingénieur·e Civil spécialisé·e dans l’aménagement et la renaturation de cours d’eau.Si vous souhaitez mettre vos compétences au service de projets à forte valeur environnementale, tout en évoluant dans une équipe dynamique et engagée, cette
- 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,
- Suisse Romande | Sion | CDIJe recrute pour le compte de l’un de mes clients un·e Directeur·trice de travaux spécialisé·e dans les aménagements de cours d'eau. Basé·e en Suisse romande, vous intégrerez une équipe expérimentée, au cœur de projets techniques ambitieux et variés.Vos missionsSous la supervision du chef de section, vous serez en charge de :Participer à l’élaboration des appels d’offres (cahiers des charges, analyses, etc.).Assurer laSuisse Romande | Sion | CDIJe recrute pour le compte de l’un de mes clients un·e Directeur·trice de travaux spécialisé·e dans les aménagements de cours d'eau. Basé·e en Suisse romande, vous intégrerez une équipe expérimentée, au cœur de projets techniques ambitieux et variés.Vos missionsSous la supervision du chef de section, vous serez en charge de :Participer à l’élaboration des appels d’offres (cahiers des charges, analyses, etc.).Assurer la
- For one of our clients, a world leader in the CDMO industry and biotechnology, we are currently looking for a Bioprocess Engineer (Downstream).General Information:Start date: 01.11.2025Duration: until 31.10.2026Workplace: VispWorkload: 100%Remote/Home Office: No, fully onsiteWorking hours: StandardOur client’s site in Visp, Switzerland is growing and for their Biologics organization, we are seeking experienced Bioprocess Engineers with significant workFor one of our clients, a world leader in the CDMO industry and biotechnology, we are currently looking for a Bioprocess Engineer (Downstream).General Information:Start date: 01.11.2025Duration: until 31.10.2026Workplace: VispWorkload: 100%Remote/Home Office: No, fully onsiteWorking hours: StandardOur client’s site in Visp, Switzerland is growing and for their Biologics organization, we are seeking experienced Bioprocess Engineers with significant work
- For our Client in Visp we are searching for a Technical Document Manager who is responsible for coordinating the creation, adaptation, version control, and approval workflows of key project documentation throughout all project phases. Key Responsibilities: Responsible for performance qualification (PQ) from detailed design through execution. This includes both CapEx-driven mechanical adaptations managed by external engineering (EPCM) partner and OpExFor our Client in Visp we are searching for a Technical Document Manager who is responsible for coordinating the creation, adaptation, version control, and approval workflows of key project documentation throughout all project phases. Key Responsibilities: Responsible for performance qualification (PQ) from detailed design through execution. This includes both CapEx-driven mechanical adaptations managed by external engineering (EPCM) partner and OpEx
- 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 &
