Descripción de la oferta
MSAT Scientist – Biologics ManufacturingAsegúrese de que toda la información de su solicitud está actualizada y en orden antes de inscribirse en esta oportunidad.Spain | Full-time | On-site | Biopharmaceutical ManufacturingWe are supporting a global biologics and vaccine manufacturing organisation looking to hire an MSAT Scientist to join their Manufacturing Science & Technology team within a GMP-regulated biologics environment.This is a hands-on operational role supporting manufacturing, process performance, technology transfer and continuous improvement activities across biologics production processes. The position works closely with Manufacturing, QA, QC and Engineering teams within a fast-paced GMP manufacturing environment.The RoleYou will support MSAT and manufacturing activities linked to process monitoring, troubleshooting, process validation and technology transfer within biologics manufacturing operations.Key responsibilities include:Supporting manufacturing process monitoring and troubleshooting activitiesAssisting with technology transfer and process validation activitiesSupporting GMP manufacturing operations across upstream and/or downstream processesReviewing and generating GMP documentation including SOPs, batch records, protocols and technical reportsSupporting deviation investigations, root cause analysis and CAPA activitiesCollaborating cross-functionally with Manufacturing, QA, QC and Engineering teamsSupporting continuous improvement and process optimisation initiativesEnsuring activities are carried out in compliance with GMP and quality standardsYour ProfileWe’re looking for candidates with hands-on experience within a GMP-regulated biologics or biopharmaceutical manufacturing environment.This role is best suited to candidates coming from:MSAT / MS&TGMP ManufacturingProcess DevelopmentManufacturing SupportTechnology TransferTechnical Operationswithin biologics, vaccines, biosimilars or biopharmaceutical production environments. xcskxlj You will ideally have:2+ years industry experience within biopharmaceutical manufacturingExperience supporting GMP manufacturing operationsExposure to upstream and/or downstream biologics processesExperience working with GMP documentation, SOPs and batch recordsExposure to deviations, investigations, CAPAs or process troubleshootingFamiliarity with process validation, technology transfer or manufacturing support activitiesDegree background in Biotechnology, Biochemistry, Chemical Engineering, Bioprocess Engineering or related scientific disciplineEnglish language skills required; Spanish is advantageousExperience from biologics manufacturing companies or CDMO environments is highly advantageous.Why ApplyStrong exposure to biologics manufacturing and technology transfer activitiesOpportunity to develop within an MSAT / technical operations environmentCross-functional visibility across Manufacturing, QA, QC and EngineeringCollaborative GMP biologics manufacturing environmentLong-term development opportunities within a growing international organisation
