Validation Engineer | Validierungsingenieur (m/w/d)

Job Summary

As a Validation Engineer in the pharmaceutical industry, you will be responsible for the qualification and validation of production and laboratory equipment, GxP-regulated rooms, and technical building services. Your daily activities include managing technical change controls, overseeing measurements during qualification activities, and maintaining the validated state of equipment throughout its lifecycle. You will act as a critical liaison between quality, compliance, and technical units, ensuring all systems meet stringent regulatory standards. This role is particularly attractive due to its high level of responsibility in international cGMP audits and inspections, offering a chance to work at a leading pharmaceutical site in Ingelheim. The position provides a competitive salary package, flexible working hours with partial home office options, and extensive professional development opportunities through e-learning and wellness programs.