Found Description
We are seeking a Validation Engineer to support validation and CQV activities for pharmaceutical and biopharmaceutical projects. The successful candidate will be responsible for ensuring equipment, facilities, utilities, and systems are validated in accordance with GMP requirements and regulatory standards while supporting project delivery from commissioning through operational readiness.
ResponsibilitiesExecute commissioning, qualification, and validation (CQV) activities for GMP-regulated pharmaceutical and biopharmaceutical facilities.
Prepare, review, and maintain validation documentation, including Validation Plans, IQ/OQ/PQ protocols, test scripts, and validation reports.
Perform validation of equipment, utilities, facilities, and computerized systems in compliance with GMP, GAMP 5, FDA 21 CFR Part 11, and applicable regulatory requirements.
Coordinate with project engineers, qualit...