Descripción de la oferta
MSAT Scientist – Biologics Manufacturing Spain | Full-time | On-site | Biopharmaceutical Manufacturing We 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 Role You 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 activities Assisting with technology transfer and process validation activities Supporting GMP manufacturing operations across upstream and/or downstream processes Reviewing and generating GMP documentation including SOPs, batch records, protocols and technical reports Supporting deviation investigations, root cause analysis and CAPA activities Collaborating cross-functionally with Manufacturing, QA, QC and Engineering teams Supporting continuous improvement and process optimisation initiatives Ensuring activities are carried out in compliance with GMP and quality standards Your Profile We’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&T GMP Manufacturing Process Development Manufacturing Support Technology Transfer Technical Operations within biologics, vaccines, biosimilars or biopharmaceutical production environments. You will ideally have: 2+ years industry experience within biopharmaceutical manufacturing Experience supporting GMP manufacturing operations Exposure to upstream and/or downstream biologics processes Experience working with GMP documentation, SOPs and batch records Exposure to deviations, investigations, CAPAs or process troubleshooting Familiarity with process validation, technology transfer or manufacturing support activities Degree background in Biotechnology, Biochemistry, Chemical Engineering, Bioprocess Engineering or related scientific discipline English language skills required; Spanish is advantageous Experience from biologics manufacturing companies or CDMO environments is highly advantageous. Why Apply Strong exposure to biologics manufacturing and technology transfer activities Opportunity to develop within an MSAT / technical operations environment Cross-functional visibility across Manufacturing, QA, QC and Engineering Collaborative GMP biologics manufacturing environment Long-term development opportunities within a growing international organisation
