EMES Validation Specialist — CSV, EBR & Data Integrity

An established industry player is seeking a Specialist to execute validation activities for the S12 Enterprise Manufacturing Execution System (EMES) in cell therapy manufacturing. This role involves working collaboratively with various teams to ensure compliance with health authority regulations and maintain data integrity. The ideal candidate will possess a strong understanding of electronic batch records and validation processes, along with the ability to manage technical documentation effectively.

This position offers an exciting opportunity to contribute to the advancement of manufacturing technologies in a dynamic environment, supporting critical operations and ensuring quality standards are met.
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