Descripción de la oferta
MSAT Scientist – Biologics Manufacturing
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 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 standardsYour 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 advantageousExperience 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
