We are working a leading Systems Integrator company working onsite at a pharmaceutical manufacturing facility in South Dublin.
The role supports the expansion of site automation across production operations, troubleshooting, and system optimisation in a GMP-regulated environment.12-month contract initially with long-term placement potential.
Up to €70/hour DOEJob Responsibilities Act as System Owner for automation assets, ensuring lifecycle management, maintenance, and validation.
Provide on-floor and remote technical support for production, shutdowns, and troubleshooting.
Lead or support investigations, root-cause analysis, and CAPA implementation.
Manage change controls, deviations, and system documentation in compliance with GMP standards.
Deliver automation improvements, control system upgrades, and support digitalisation initiatives.
Support new product introductions, engineering projects, and cross-functional collaboration.
Ensure all automation activities comply with EHS and regulatory requirements.
Job Requirements Degree in Automation, Electrical, Computer, Chemical, or Biotech Engineering (or related field).
Minimum 5 years' experience in automation within a GMP manufacturing environment.
Strong Allen-Bradley (Rockwell) PLC and HMI experience is essential.
Experience with Siemens PLCs, SCADA systems (Factory Talk View, i Fix, In Touch, Zenon) an advantage.
Familiarity with fieldbus systems (Control Net, Device Net, Profibus, Profinet, AS-i, etc.).
Knowledge of GAMP 5, ISA-88/95, and relevant regulatory standards (21 CFR Part 11, Annex 11).
Working knowledge of network architecture (TCP/IP, Firewalls).
Strong documentation, troubleshooting, and stakeholder communication skills.
Self-driven, organised, and comfortable working across multiple projects in a GMP setting