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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,
- 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,
- Role OverviewWe are seeking an experienced Privileged Access Management (PAM) Subject Matter Expert (SME) to lead the design, implementation, and operational maturity of PAM capabilities across a complex enterprise environment.This role is responsible for establishing and enforcing robust security controls for privileged identities, ensuring compliance with regulatory and security standards, and embedding PAM as a core enterprise security capability.TheRole OverviewWe are seeking an experienced Privileged Access Management (PAM) Subject Matter Expert (SME) to lead the design, implementation, and operational maturity of PAM capabilities across a complex enterprise environment.This role is responsible for establishing and enforcing robust security controls for privileged identities, ensuring compliance with regulatory and security standards, and embedding PAM as a core enterprise security capability.The
- For our client, an international company based in Visp, we are looking for a Plant Engineer - Utilities.The Process Engineer is responsible for the seamless planning, realization, and optimization of chemical and biological production facilities. This role serves as a technical backbone for plant efficiency, ensuring that all modifications and maintenance activities meet the highest standards of safety and regulatory compliance within a fast-pacedFor our client, an international company based in Visp, we are looking for a Plant Engineer - Utilities.The Process Engineer is responsible for the seamless planning, realization, and optimization of chemical and biological production facilities. This role serves as a technical backbone for plant efficiency, ensuring that all modifications and maintenance activities meet the highest standards of safety and regulatory compliance within a fast-paced
- 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 &
