Réalta Technologies are looking for a CSV Engineer to support a pharmaceutical client in Carlow, Ireland. This is an exciting opportunity to join a regulated manufacturing environment and support compliance, validation, and data integrity activities across site systems.
Responsibilities
- Support CSV and compliance activities across IT and automation systems.
- Ensure compliance with SDLC, CSV, IT Security, and Data Integrity requirements.
- Assist with:
- Change controls
- Periodic reviews
- System administration and access management
- Deviations, investigations, and CAPAs
- Disaster recovery and audit support
- Work in line with GMP regulations including EU Annex 11 and 21 CFR Part 11.
- Collaborate with cross-functional teams to support continuous improvement and site compliance.
Requirements
- Degree qualification in Science, Engineering, IT, or a related discipline.
- 3–5 years’ experience in Computer System Validation within pharmaceutical, life sciences, or medical device environments.
- Strong understanding of GxP-regulated environments and validation processes.
- Good communication and teamwork skills.
