Site Automation Lead – Pharma, OT & Digital Manufacturing

Takeda

Bray

On-site

EUR 72,000 - 99,000

Full time

14 days+

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Job summary

Takeda in Bray, Ireland, is seeking a senior automation leader to define and deliver the site automation strategy within a cGMP pharma manufacturing environment. You will own automation systems across PLC, SCADA, historian, and related platforms, driving reliability, compliance, and future-ready digital enablement.

You will lead a high-performing team, collaborate with Manufacturing, Quality, IT, and external partners, and ensure cyber resilience, lifecycle management, and audit readiness across

Qualifications

  • Degree qualification in Automation, Electrical, Industrial, or related discipline.
  • 7+ years in automation or OT, with 2+ years in leadership.
  • Strong PLC/SCADA and industrial automation experience.
  • Experience in regulated pharma/biotech GMP environment.
  • Knowledge of data integrity, validation and change control.

Responsibilities

  • Define, lead and continuously improve the site automation strategy in alignment with site priorities and global automation standards.
  • Lead, coach and develop the site automation team, building capability, resilience and knowledge transfer.
  • Own the technical availability, operation, maintenance and lifecycle management of automation and OT systems.
  • Plan and execute automation projects and site investment initiatives, ensuring delivery, compliance and cost control.
  • Provide automation leadership for manufacturing, utilities, facilities and process equipment; troubleshoot and support CAPA.

Skills

Leadership
Cross-functional collaboration
Strategic planning
Problem solving

Education

Degree qualification in Automation, Electrical, Industrial, Control Systems, Computer Science, Engineering or related

Tools

PLC
SCADA
Networked control systems
Virtualised environments
Industrial automation infrastructure

Job description

Takeda in Bray, Ireland, is seeking a senior automation leader to define and deliver the site automation strategy within a cGMP pharma manufacturing environment. You will own automation systems across PLC, SCADA, historian, and related platforms, driving reliability, compliance, and future-ready digital enablement.

You will lead a high-performing team, collaborate with Manufacturing, Quality, IT, and external partners, and ensure cyber resilience, lifecycle management, and audit readiness across

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