Senior MES Consultant (Biopharmaceutical / Bioprocess Manufacturing)

Job Description Job Description The Senior MES Consultant will drive the delivery of an MES project within a GMP-regulated bioprocess manufacturing environment, combining strong MES expertise with hands-on bioprocess knowledge to deliver a compliant, robust solution. Key Responsibilities Lead and drive the MES project end-to-end. Act as the senior MES lead and main point of contact for client stakeholders. Gather requirements and translate bioprocess manufacturing workflows into MES solutions. Oversee MBR / EBR design, configuration and integration with ERP, automation and other site systems. Ensure compliance with GMP, CSV / GAMP 5, 21 CFR Part 11 and data integrity requirements. Coordinate the project team, timelines, risks and progress reporting. Requirements Degree in engineering, life sciences, computer science or a related discipline. 10+ years' experience in life sciences manufacturing systems, including lead-level MES delivery. Strong background in biopharmaceutical / bioprocess manufacturing. Hands-on experience with a leading MES platform (e.g., PAS-X, Syncade, PharmaSuite, Opcenter). Sound knowledge of GMP, CSV / GAMP 5, ISA-95 and data integrity. Strong leadership, communication and stakeholder management skills. Based in, or willing to relocate to, St. Louis, Missouri, and authorized to work in the US. #J-18808-Ljbffr Advanced Manufacturing Tech Solutions PTE. LTD. (AMTSOL)