Infrastructure ensure audit readiness and address findings. Support BioAtrium Operations objectives, proactively flag operational issues, and ensure timely communication across teams. Act in accordance with Safety, Health and Environmental policies; proactively identify risks and support SHE improvement initiatives. Participate in continuous improvement programs (Lean, operational excellence) and support training by sharing equipment/system expertise. Maintain up-to-date knowledge of industry standards, new technologies, and regulatory expectations. Your profile Minimum 5 years of experience in a relevant engineering/technical field (ideally GMP‑regulated pharma/biotech manufacturing). Strong GMP mindset with hands‑on experience in documentation and quality systems (deviations, change controls, CAPA, investigations). Proven troubleshooting capability and structured problem‑solving (RCA). Experience contributing to CAPEX projects and equipment lifecycle activities (from selection to commissioning/qualification). Languages: German and English (professional level) required. Availability: full‑time onsite in Visp; temporary assignment (~1 year) as maternity leave cover. #J-18808-Ljbffr
