Senior CQV Engineer: Validation Lead for Pharma

A multinational pharmaceutical company located in the Netherlands is seeking a Senior CQV Expert to lead validation and requalification activities for critical systems within a manufacturing environment. The role focuses on ensuring compliance with regulatory standards and internal quality procedures while managing projects and deviations. Candidates should possess a bachelor's degree and 4-5 years of relevant experience in validation, with strong skills in GMP, problem-solving, and project management. This position offers the opportunity to work in a dynamic environment committed to quality and continuous improvement. #J-18808-Ljbffr