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We are working with a leading biopharmaceutical manufacturer who are seeking an MSAT Bioprocess Engineer to support the technology transfer of biologics processes from development into GMP manufacturing. This role is central to ensuring smooth scale‑up, robust documentation, and ongoing process improvements within a compliant Quality Management System.
Job Responsibility:
Lead the technology transfer of new and existing biologics processes into GMP manufacturing
Prepare, review, approve and issue GMP manufacturing documentation, including batch records
Define scale‑up criteria and develop process mass balances and flow diagrams
Specify large‑scale equipment and assess material suitability for GMP use
Generate quality documentation for raw materials and equipment
Work within the site Quality Management System, raising and managing change controls
Conduct and close investigations, deviations and CAPAs
Project manage the introduction of processes into manufacturing from end to end
Perform risk assessments aligned with ICH Q9 principles
Collaborate cross‑functionally with MSAT, Development, Manufacturing, QA, Supply Chain, Engineering and Project Management teams, as well as relevant external partners
Requirements:
BSc (Hons) or equivalent in a Science or Engineering discipline
Proven GMP biologics manufacturing or process development experience
Strong organisational and stakeholder influencing skills
Demonstrated project management capability and ability to meet deadlines
Experience in process scale‑up/transfer and providing manufacturing support
Effective communication across all levels
Experience evaluating materials for process suitability and writing GMP batch records
Nice to have:
Commercialisation and process validation
Process improvement and process mapping
Defining, sourcing and validating large‑scale bioprocessing equipment