Description
The Computer System Validation Specialist will plan, coordinate, and execute validation, qualification, calibration, risk management, security, deviation, change, and lifecycle review activities for computer-assisted systems in a pharmaceutical environment. The role also manages GMP-related documentation and serves as the first point of contact for validation questions. Candidates need a degree in computer science or natural sciences, several years of pharmaceutical Quality Management experience, GAMP5 knowledge, strong organizational and communication skills, and excellent German and English proficiency. The employer offers flexible working hours, 30 days of vacation, training opportunities, and additional employee benefits.
