SR MES Consultant

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.

•      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.

•      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.