7 supporter jobs found in Valais.

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,

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 work

Commissioning Qualification Validation Engineer For our Client in Visp we are searching for a Commissioning Qualification Validation Engineer (CQV) to carry out a variety of tasks related to the validation of equipment and facilities.Key Responsibilities:CQV validation activities including but not limited to: Facilities, Utilities, Validation Life Cycle, Execution, Technical Documentation, Process, GAP Analysis and Risk Assessment.Coordination of the

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 &

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 OpEx

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,

Randstad est une entreprise internationale de services en ressources humaines, leader et innovante, qui propose une gamme complète de services. Nous sommes spécialisés dans le conseil global et les prestations efficaces dans le domaine des ressources humaines. Travailler chez Randstad est différent de travailler dans une seule organisation. Car chez Randstad, nous plaçons les personnes au centre de nos activités. Cela vaut pour nos clients, nos candidats,