A leading consulting firm in pharmaceuticals is seeking an experienced QA Specialist, CSV & Automation in Visp, Switzerland, to support large-scale CAPEX projects within a GMP-regulated environment. The role involves ensuring qualification and validation compliance for equipment and computerized systems, overseeing projects from inception to execution, and providing QA leadership. Ideal candidates have a degree in Engineering or Life Sciences, significant GMP experience, and fluency in English. Knowledge of German is advantageous. #J-18808-Ljbffr