
CSV Engineer
- Galway
- Permanent
- Full-time
- Lead validation and Computer Software Assurance (CSA) for IT and OT systems
- Develop and execute protocols (IQ/OQ/PQ/PPQ, Test Method Validation)
- Provide risk-based validation guidance aligned with GxP, FDA, and EU MDR requirements
- Partner cross-functionally with QA, IT, Engineering, and Manufacturing
- Support system and process improvements that enhance quality, compliance, and efficiency
- Utilize tools like Excel and Minitab for data analysis and reporting
- 5+ years of experience in computer system validation or software assurance in a regulated environment (medical device/pharma)
- Deep knowledge of 21 CFR Part 11, 21 CFR 820, ISO 13485, and GAMP/CSA methodology
- Strong understanding of IT/OT systems (e.g., MES, SCADA, ERP, LIMS, Data Historians)
- Proven experience developing validation plans, protocols, and risk assessments
- Excellent communication and documentation skills
- Experience validating manufacturing automation systems (MES, PLC, SCADA)
- ASQ Software Quality Engineer certification
- Familiarity with Six Sigma or TQM principles