A leading consulting firm in Life Sciences is seeking a CSV Consultant to contribute to the validation of computerized systems in regulated environments. This role focuses on ensuring compliance with GxP regulations and supporting quality in pharma and biotech organizations. Ideal candidates will have a Master’s degree, and experience in CSV, QA, or IT compliance, along with fluency in English and Dutch. Join a dynamic team and make a meaningful impact in the digital transformation journey. #J-18808-Ljbffr