MES Program Manager

Must Haves:
10 years of IT program or project management experience with a minimum of 5 years specifically managing MES implementations in Life Sciences Biopharma or GMP-regulated manufacturing

ERP Integration: SAP S/4HANA PP/MM/EWM or equivalent ERP covering production order execution material consumption (goods issue/receipt) batch/lot management and MES EWM warehouse staging flows.

Enterprise ecosystem: functional understanding of LIMS (Labware Benchling or equivalent) QMS/QDMS (Veeva Vault or equivalent) Historian (OSI PI or equivalent) and IT/OT (OPC UA/DA DeltaV SCADA).

Integration architecture: IDocs REST/SOAP APIs SAP PI/PO or equivalent middleware; understanding of synchronous vs. asynchronous messaging error handling and integration monitoring in GMP environments.

GxP/CSV: GAMP 5 21 CFR Part 11 Annex 11 ALCOA IQ/OQ/PQ protocols RTM structure and change control governance in a validated system environment.


JD:
Own and manage the full MES program lifecycle - pre-implementation implementation testing and go-live - for Werum PAS-X

Lead the definition and delivery of all MES pre-implementation outputs: scope statement process design confirmation functional requirements data readiness fit-gap analysis and implementation timeline.

Oversee Electronic Batch Record (EBR) design and workflow development ensuring manufacturing processes are correctly modeled in PAS-X aligned with ISA-88 standards.

Drive the fit-gap analysis process coordinating business analysts and SMEs to identify gaps between standard PAS-X capabilities and NCF business requirements with resolution strategies documented.

Manage MES vendor and system integrator relationships holding delivery teams accountable to milestones quality standards and contractual obligations.

Oversee MES configuration recipe authoring master batch record (MBR) design and system validation activities in coordination with QA and validation teams.

Lead the end-to-end integration program between MES (PAS-X) and ERP (SAP S/4HANA or equivalent) defining all interface touchpoints data flows and middleware architecture.

Establish and maintain program governance structures: integrated master schedule RAID log decision register change control log and steering committee reporting cadence.

Define and track program milestones across MES integration and validation workstreams providing timely escalation when scope schedule or quality risks emerge.

Facilitate cross-functional workshops design reviews and integration alignment sessions across Manufacturing Quality IT/OT Supply Chain and Enterprise Architecture teams.

Communicate program status risks and key decisions to senior leadership and executive sponsors in clear concise and executive-ready formats.

Ensure all MES and integration deliverables comply with GMP GxP 21 CFR Part 11 GAMP 5 and ALCOA requirements throughout the program lifecycle.