CGREG is currently seeking a CSV Validation Engineer with experience in automation platforms within the pharmaceutical industry on a long-term contract.
Key Responsibilities:
* Participate and lead CSV activities linked to Automation projects
* Support the preparation of lifecycle documents, including validation plans, requirement specifications, risk assessments, qualification protocols, requirements traceability matrices, and validation reports.
* Design, generate, and execute test plans and test protocols, managing and reporting findings and non-conformances raised during all types of testing.
Requirements:
* Third level qualification in Electrical, Electronic, Systems Engineering, Computer Science or Equivalent
* 5+ years experience working in control systems validation in the Life Sciences/Pharma sector
Valid Irish work permit required.