A leading technology firm in Cork is seeking a Mid-Level CSV Engineer to support validation activities for GMP-regulated computerized systems.
The ideal candidate will have 4–7 years of experience in Computer System Validation within a regulated pharma/biopharma environment, and possess strong documentation and collaboration skills.
The role requires execution of CSV lifecycle deliverables ensuring compliance with regulations.
Applicants should hold a relevant Bachelor's degree and have a solid understanding of GAMP guidelines.
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