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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.
If you are considering sending an application, make sure to hit the apply button below after reading through the entire description.
12-month contract initially with long-term placement potential.
Up to €70/hour DOE
Job 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 (FactoryTalk View, iFix, InTouch, Zenon) an advantage.
- Familiarity with fieldbus systems (ControlNet, DeviceNet, 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). xcfaprz
- Strong documentation, troubleshooting, and stakeholder communication skills.
- Self-driven, organised, and comfortable working across multiple projects in a GMP setting
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Sprachkenntnisse
- English
Hinweis für Nutzer
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