Senior MES Lead - Bioprocess & GMP Solutions

Advanced Manufacturing Tech Solutions (AMTSOL)

St. Louis (MO)

On-site

USD 140,000 - 190,000

Full time

5 days ago
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Job summary

Advanced Manufacturing Tech Solutions (AMTSOL) seeks a Senior MES Consultant to lead MES delivery in a GMP-regulated bioprocess environment. You will translate bioprocess workflows into MES solutions and oversee design and integration with ERP and automation systems.

The role requires extensive MES platform experience (PAS-X, Syncade, PharmaSuite, Opcenter) and strong GMP/CSV knowledge, with a focus on data integrity and regulatory compliance. Missouri-based relocation is supported.

Qualifications

  • 10+ years of experience in life sciences manufacturing systems with lead-level MES delivery.
  • Strong background in biopharmaceutical / bioprocess manufacturing.
  • Based in, or willing to relocate to, St. Louis, Missouri, and authorized to work in the US.
  • Hands-on experience with a leading MES platform (PAS-X, Syncade, PharmaSuite, Opcenter).

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.

Skills

Leadership
Communication
Stakeholder management

Education

Engineering, Life Sciences, Computer Science degree or related

Tools

PAS-X
Syncade
PharmaSuite
Opcenter

Job description

Advanced Manufacturing Tech Solutions (AMTSOL) seeks a Senior MES Consultant to lead MES delivery in a GMP-regulated bioprocess environment. You will translate bioprocess workflows into MES solutions and oversee design and integration with ERP and automation systems.

The role requires extensive MES platform experience (PAS-X, Syncade, PharmaSuite, Opcenter) and strong GMP/CSV knowledge, with a focus on data integrity and regulatory compliance. Missouri-based relocation is supported.

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