A leading technology firm in Cork is seeking a Computer System Validation (CSV) Engineer with experience in Manufacturing Execution Systems (MES).
The role ensures that computerized systems are validated to meet GMP standards and regulatory compliance.
Key responsibilities include executing validation lifecycles, developing validation documentation, and collaborating with various teams during system implementations.
The ideal candidate will possess a relevant degree and have 3-6 years of experience in the pharmaceutical or biotech industry.
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