DeltaV CSV Engineer - Hybrid, Growth & Impact

Simotechnology

Limerick

Hybrid

EUR 70,000 - 90,000

Full time

14 days+

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Job summary

SimoTech in Limerick is seeking a DeltaV CSV Engineer to support a biotech manufacturing facility for a multinational biopharma client. You will validate computerised systems within the process automation framework to ensure compliance with industry standards.

The ideal candidate has 5+ years’ CSV experience in pharma, hands-on DeltaV and Siemens PLC validation, and strong cross‑functional communication. This role offers a hybrid work model, ongoing training, and exposure to advanced

Qualifications

  • Bachelor’s degree in Engineering, Information Systems, Computer Science or Life Sciences.
  • Minimum of 5 years’ experience as a CSV Engineer in a pharmaceutical environment.
  • Hands-on experience validating DeltaV and Siemens PLC systems.
  • Knowledge of 21 CFR Part 11, EU Annex 11 and GAMP5.
  • Experience with risk management tools like FMEA.
  • Strong written and verbal communication and cross-functional collaboration.

Responsibilities

  • Create and execute validation strategies for new or existing process automation systems.
  • Assist with validation of DeltaV, Siemens PLC, and other systems.
  • Write and review URS, FRS, IQ, OQ, PQ, and Validation Plans.
  • Carry out risk assessments and address deviations.
  • Create traceability matrices and manage change controls.
  • Prepare validation summary reports and support audits/inspections.
  • Ensure compliance with 21 CFR Part 11, EU Annex 11, and GAMP5.
  • Collaborate with Quality Assurance to close compliance gaps.

Skills

DeltaV
Process automation
Risk management
Cross-functional teamwork
Communication
Attention to detail

Education

Bachelor’s degree in Engineering/Information Systems/Computer Science/Life Sciences

Tools

Siemens PLC
FMEA

Job description

SimoTech in Limerick is seeking a DeltaV CSV Engineer to support a biotech manufacturing facility for a multinational biopharma client. You will validate computerised systems within the process automation framework to ensure compliance with industry standards.

The ideal candidate has 5+ years’ CSV experience in pharma, hands-on DeltaV and Siemens PLC validation, and strong cross‑functional communication. This role offers a hybrid work model, ongoing training, and exposure to advanced

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