SRG has a client who are a global name in the pharmaceutical industry. This role sits within their GMP production team and is accountable for the oversight of batches manufactured in cleanrooms, supporting the delivery of manufacturing projects to agreed timelines, quality standards and budgets.

SRG 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.