Job Description In this role, you’ll be a key member of our Qualification & Validation Team, specializing in the validation of computerized systems. Your work will ensure our systems meet the highest quality standards—playing a vital part in our mission to advance cancer treatment and make a lasting difference in patients' lives. You’ll plan, coordinate, and execute CSV tasks in manufacturing, quality control, and logistics at our GMP-certified site in Bergisch Gladbach. From URS and risk assessments to IQ/OQ protocols, reports, and SOPs—you’ll handle all documentation with precision and care. You’ll guide departments through validation projects, propose effective solutions, and oversee their implementation. As a GxP expert, you’ll be involved in deviation handling, CAPA, change control, and continuously improve validation-related procedures. You’ll work closely with internal stakeholders (IT, QA, QC, Manufacturing) and external vendors, and deliver training based on your activities.