Descripción de la oferta
Asegúrese de que toda la información de su solicitud está actualizada y en orden antes de inscribirse en esta oportunidad.Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? We are looking for a Process Validation Specialist to support validation activities related to aseptic filling operations within a GMP-regulated pharmaceutical manufacturing environment.ResponsibilitiesSupport the planning and execution of process validation activities related to filling operations.Participate in Process Performance Qualification (PPQ) activities and other validation lifecycle activities.Support data collection and analysis during validation runs and routine manufacturing.Collaborate with Manufacturing, Quality Assurance, and Engineering teams to ensure GMP compliance.Assist with risk assessments and continuous improvement initiatives for manufacturing processes.QualificationsBachelor’s or Master’s degree in Pharmaceutical Sciences, Biotechnology, Chemical Engineering, Life Sciences, or a related field.Minimum 1 year of experience in the pharmaceutical, biotechnology, or related regulated industry (internships or thesis projects are also considered).Basic knowledge of GMP and pharmaceutical manufacturing processes.Fluent in English and Spanish.PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.
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