Support MES validation activities for Electronic Batch Record systems.

Review validation packages, including protocols, test scripts, reports, and supporting documents.

Review and assess URS, functional specifications, data mapping, and validation documentation.

Support execution or review of MES validation testing, where required.

Ensure validation activities comply with GMP, GDP, and data integrity requirements.

Collaborate closely with Manufacturing, Quality, Validation, Automation, and IT teams.

Identify documentation gaps and support remediation or follow‑up actions.

Ensure Electronic Batch Record workflows are aligned with shopfloor manufacturing operations.

Support audit readiness by maintaining clear and complete validation documentation.

Experience in MES validation within pharma, biotech, or GMP‑regulated manufacturing.