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Sr. Techno-Functional Consultant – Manufacturing OTIT Integration & MES

Iconma Portal

Job Location:

Parsippany, NJ - USA

Hourly Salary: USD 60 - 64

Posted: 22 October 2026 (Yesterday)

Application Deadline: 19 January 2027

Vacancies: 1 Vacancy

Job Summary

Our Client an IT Services and Consultant company is looking for a Sr. Techno-Functional Consultant Manufacturing OT/IT Integration & MES for their Parsippany NJ location.

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

Requirements:

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
Top Skills:
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