Senior GMP Documentation & CAPA Specialist

A leading biopharmaceutical company in Verona is seeking a talented professional to manage GMP documentation, focusing on deviations and change controls. You will be responsible for drafting and standardizing high-quality records and ensuring compliance with regulations. The ideal candidate should have a BS/BA in a scientific field and significant experience in GMP environments. The role offers competitive salaries and excellent benefits, along with opportunities for growth in a dynamic setting. #J-18808-Ljbffr