MSAT Scientist

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