DeltaV Automation Engineer – GMP Pharma DCS Expert

CG Controls Ltd.

Tipperary

On-site

EUR 70,000 - 90,000

Full time

2 days ago
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Job summary

CG Controls Ltd. seeks an experienced DeltaV Automation Engineer to support design, configuration, commissioning, validation and lifecycle management of DeltaV control systems in a regulated pharmaceutical environment.

The role collaborates with Automation, Engineering, Manufacturing, Quality and IT/OT to deliver compliant process automation solutions in line with GMP, site standards and regulatory requirements. On-site attendance during commissioning and start-up is required.

Qualifications

  • Degree in Automation, Electrical, Chemical or related discipline.
  • 5+ years in industrial automation or process control.
  • Minimum 3 years hands-on Emerson DeltaV experience.
  • Experience in pharmaceutical or other regulated manufacturing.
  • Good understanding of GMP lifecycle requirements.

Responsibilities

  • Design, configure, test, and commission DeltaV DCS applications.
  • Develop and modify CM, EMS, Phases and recipes, batch control logic & Alarm configuration.
  • Support DeltaV Batch configuration including recipes, unit procedures and phases.
  • Develop automation solutions per FS, DS and site automation standards.
  • Prepare/review URS documentation, test protocols and scripts.
  • Commissioning and qualification documentation.
  • Execute FAT, SAT, commissioning and qualification activities.
  • Support IQ/OQ/PQ, CSV and CSA activities as required.
  • Troubleshoot DeltaV hardware, software, networks and interfaces.
  • Integrate DeltaV with MES/SCADA/BMS and other systems.

Skills

DeltaV automation
GMP compliance
Process control troubleshooting

Education

Bachelor's degree in Automation or related field

Tools

Emerson DeltaV
OSIsoft PI
ISA-88

Job description

CG Controls Ltd. seeks an experienced DeltaV Automation Engineer to support design, configuration, commissioning, validation and lifecycle management of DeltaV control systems in a regulated pharmaceutical environment.

The role collaborates with Automation, Engineering, Manufacturing, Quality and IT/OT to deliver compliant process automation solutions in line with GMP, site standards and regulatory requirements. On-site attendance during commissioning and start-up is required.

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