Validation Engineer

We are currently hiring for a Process Validation Engineer to support a global plasma-derived therapeutics manufacturer at an active GMP manufacturing site in Vista, CA . The Validation Engineer will work directly alongside site validation and manufacturing teams, supporting hands-on process validation activities tied to ongoing operations and project work.

The focus is execution, data generation, and documentation. This is not a coordination, oversight, or strategy-only role. You will be actively executing protocols, supporting validation runs, compiling data, and contributing to deliverables that support inspection readiness.

This opportunity is well suited for a junior to mid-level validation engineer looking to gain strong, real-world process validation experience at a regulated manufacturing site.

Key Responsibilities

• Execute approved process validation protocols for new and modified manufacturing processes
• Support validation execution activities related to process, equipment, cleaning, and / or facilities as needed
• Collect, compile, and verify raw validation data for accuracy and completeness
• Support protocol deviations and investigations in accordance with GMP requirements
• Assist with preparation of validation summary reports
• Maintain validation documentation and project files in an inspection-ready state
• Work cross-functionally with Manufacturing, Validation, QA, and external qualification resources during execution

Required Experience