Job description: Start: Asap Duration: 1 year with possible extension Workload: 100% Location: Visp (on-site, no home office) Requirements: Lead technical expansion and capacity-increase projects within Drug Product manufacturing to support production ramp-up Provide technical and operational input to project design, ensuring compliance with GMP and regulatory standards, including EU GMP Annex 1 Coordinate cross-functional teams and external suppliers, supporting project governance and ensuring delivery within scope, budget and timelines Develop and implement best-practice processes aligned with current industry expectations and regulatory trends Manage project-related change controls, troubleshooting and deviations, including equipment-related investigations Establish and update operational procedures in close collaboration with manufacturing and quality teams Competences: Minimum 2 years of technical experience in GMP manufacturing (Drug Product preferred) Proven experience in project coordination or project management within pharmaceutical operations CAPEX project exposure and equipment qualification experience are strong advantages Solid understanding of cGMP and Annex 1 requirements Fluent in English; German is an advantage Strong collaboration skills, proactive mindset and ability to deliver under pressure with changing priorities