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Program Manager Industrial Automation / DeltaV

Job Description - Program Manager Industrial Automation / DeltaV


We are looking for an experienced Program Manager with a strong industrial automation and IT/OT background to lead automation initiatives across multiple pharmaceutical manufacturing sites in Ireland. The role combines project delivery, client relationship management, team development and identification of new business opportunities.

Key responsibilities



  • Manage industrial automation and digital projects across multiple manufacturing sites.

  • Define and maintain project scope, budgets, quality standards and timelines.

  • Ensure projects are delivered on time, within scope and within agreed budgets.

  • Coordinate internal teams, contractors, product teams and external stakeholders.

  • Manage client communication, feedback and ongoing relationships.

  • Identify new project opportunities and support business expansion across Ireland.

  • Manage project resources, team onboarding and demand fulfilment.

  • Monitor portfolio performance and support P&L management.

  • Identify, assess and mitigate project risks.

  • Manage changes to project scope, schedules and costs.

  • Track milestones and provide regular status reporting to stakeholders.

  • Ensure compliance with pharmaceutical regulatory requirements, including GxP, CSV and SDLC.

  • Partner with product and architecture teams to develop solutions aligned with global standards.

  • Coach and manage members of the internal delivery team.






Requirements







  • Bachelor’s degree in Engineering, IT, Automation or a comparable field.

  • At least 8 years of relevant professional experience.

  • At least 5 years of recent project or program management experience.

  • Strong background in industrial automation and IT/OT project delivery.

  • Knowledge of shop-floor automation environments at ISA-95 Levels 2 and 3.

  • Experience with DeltaV and ideally PLC, SCADA, DCS or Siemens PCS 7 systems.

  • Experience in pharmaceutical, life-sciences or another GxP-regulated manufacturing industry.

  • Understanding of CSV, SDLC, change control and regulated project delivery.

  • Experience managing budgets, resources, risks, vendors and multiple parallel workstreams.

  • Excellent client-facing communication, stakeholder management and leadership skills.

  • Willingness and ability to visit multiple Irish manufacturing sites approximately four days per week.






Benefits



  • Location: Ireland

  • Contract Type: Freelance / Contract

  • Start date: September, 2026

  • Time Allocation: 40 hours/week

  • Pharmaceutical industry

  • Travelling across multiple Manufacturing sites in Ireland (Carlow, Brinnly, Dunbyone).







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