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Job Location:

St. Louis, MO - USA

Monthly Salary: Not provided by the employer
Posted: 18 October 2026 (7 days ago)
Application Deadline: 15 January 2027
Vacancies: 1 Vacancy

Job Summary

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.