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Are you ready to join aworld leaderin the exciting and dynamic fields of thePharmaceutical and Medical Device industries? We are currently seeking anexperiencedCommissioning, Qualification & Validation (CQV) Project ManagerinLeón, Spain. Lead andexecute commissioning, qualification, and validation activitiesforpharmaceutical/biotech equipmentandsystems. Prepare, review, andexecute C&Q and validation documentation( URS, DQ, IQ, OQ, PQ protocols,test scripts, andsummary reports ). Collaboratewithcross-functional teams( Engineering, QA, Validation, Manufacturing ) to ensurecompliancewithGMP,regulatory guidelines, andproject timelines. Provideproject updatesandprogress reportstostakeholders.Bachelor’s degreeinEngineering, Life Sciences, or related field. Ability to workindependentlyandcollaborativelyin aproject environment. Fluent inEnglishandSpanish( written and spoken ).PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.
