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Sr. Techno-Functional Consultant

Wise Skulls Corp.Parsippany-Troy Hills, NJ🇺🇸United StatesPosted Oct 5, 2026

Quick Overview

Seniority
Mid Senior
Work mode
Hybrid
Location
Parsippany-Troy Hills, NJ, United States
Posted
3 days ago
SAFeAgileStakeholder Management

Job Description

JD

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 andtechnical 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 Experience and Capabilities:

  • 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.

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