[Hiring] MES Design Specialist @GMP Pros, Inc.
Role Description
The MES Design Specialist provides flex coverage and independent review capacity across both workstreams. This role is not a junior support role — it requires genuine OpCenter hands-on capability, because this person may be handed a mid-complexity PI and expected to move it forward independently when one of the Lead Designers is at capacity. The Specialist also serves as the segregation-of-duties reviewer for Design Review Checklists, which means they must be competent enough to identify design errors, gaps in master data, and test case coverage issues without guidance. Think of this as a third designer with a broader mandate rather than a specific workstream.
Qualifications
- 2+ years of hands-on Siemens OpCenter Execution Pharma configuration experience — including PI design, Test-PI build, sMBR development, and MES master data creation
- Experience working in an FDA-regulated pharmaceutical manufacturing environment with demonstrated understanding of GMP requirements for electronic batch records
- Ability to perform independent DRC review (Design Review Checklist execution) for PIs designed by another engineer — this requires the ability to critically evaluate design decisions, not just check formatting
- Experience building Test-PIs aligned to Use Cases and sBMR templates for Sub-PI testing
- Working knowledge of MES master data: workcenters, equipment instances, classes, properties, statuses, and sMBR structure
- Proficiency with Kneat or equivalent electronic validation management system for validation form management and incident tracking
- Proficiency with Veeva VQD or equivalent for specification file creation and document management
- Ability to operate independently under schedule pressure and shift between workstreams fluidly without needing to be re-onboarded to each PI
Requirements
- Experience on a formal MES implementation program with a defined schedule and milestone commitments (not just maintenance or support work)
- Familiarity with transport request process and TEST/VAL/PROD environment management
- Exposure to SAP-to-MES or OSI-PI-to-MES interfaces at a conceptual level
- Prior experience functioning in a flex or cross-workstream capacity on a multi-team implementation
- Experience supporting engineering or E2E water runs in a pharmaceutical MES environment
Key Tools & Platforms
- Siemens OpCenter Execution Pharma (required, hands-on)
- Kneat (required)
- Veeva VQD (required)
- SAP (awareness)
- OSI-PI / PI System (awareness)
- Microsoft Teams / SharePoint
