PQE Group is seeking a Process Validation Specialist to support validation activities for aseptic filling operations in a GMP-regulated pharmaceutical manufacturing environment in Madrid. The role involves planning and executing validation activities, preparing documentation, and collaborating with various teams to ensure compliance.

The ideal candidate holds a Bachelor's or Master's degree in Pharmaceutical Sciences or a related field, with at least 1 year of relevant experience and fluency in English and Spanish. Join PQE Group’s dynamic and innovative environment.