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Manufacturing OT/IT Integration Lead – MES, OEE & Pharma (Techno-Functional) : Parsippany, NJ 07054 – Hybrid/Onsite

Job Title: Manufacturing OT/IT Integration Lead – MES, OEE & Pharma (Techno-Functional)

Work Location: Parsippany, NJ 07054 – Hybrid/Onsite

Exp: 9 + Years

 

Cross-Functional Coordination

•       This role requires active cross-functional coordination with business teams to ensure priorities, use case definitions, and acceptance criteria are aligned with the technical delivery roadmap.

 

Key Responsibilities

•              Translate business requirements into detailed technical specifications and solution designs for OEE, Connected Worker, and Golden Batch use cases

•              Lead and coordinate the integration workstream end-to-end; drive delivery ownership and escalation

•              Act as the primary point of contact for cross-functional stakeholders; facilitate alignment sessions across business, technical, and integration teams

•              Own technical design documents, integration specifications, and data flow diagrams

•              Govern risks/issues, project plan; represent GMSx in steering ceremonies and SAFe ceremonies

•              Drive cross-functional coordination with business teams to align priorities with technical delivery

•              Define technical implementation steps and ensure traceability between business needs and technical deliverables

•              Support UAT planning and coordinate with business stakeholders for validation

•              Provide guidance on best practices for MDF platform utilization within the GMSx program.

 

Required Qualifications & Experience

•              8+ years of experience in techno-functional roles within manufacturing, pharmaceutical, or life sciences domains

•              Proven track record of leading OT/IT integration projects and converting complex business requirements into technical solutions

•              Deep understanding of OEE calculations, batch processing workflows, and connected worker concepts in a manufacturing context

•              Strong project management skills — ability to plan, prioritize, and drive delivery independently across multiple workstreams

•              Experience guiding Computer System Validation (CSV) for Edge Gateway or similar integration platforms, preferably in GxP environments

• Familiarity with GxP-regulated environments and relevant regulatory frameworks (FDA 21 CFR Part 11, EU Annex 11)

•              Solid understanding of data management principles (data flows, naming conventions, data governance)

•              Excellent stakeholder management and communication skills — ability to align global and local teams with different priorities

•              Experience with MES (e.g., PAS-X), MDF, or similar manufacturing data/execution platforms.

 

Preferred / Nice-to-Have

•              Experience with SAFe Agile methodology in enterprise settings

•              Familiarity with ISA-95 / ISA-88 standards for manufacturing integration

•              Prior experience with large pharma/life sciences organizations

•              Knowledge of UNS (Unified Namespace) strategy and enterprise data governance frameworks

 

 

 

Avdhesh Kumar

Senior Technical Recruiter

Email: avdhesh@enterprisesolutioninc.com

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