Senior MES Consultant
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.