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.

• 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

• 2+ years of hands‑on process validation experience
• GMP manufacturing experience in pharmaceutical or biotech environments
• Recent execution experience authoring and running protocols (not review‑only)
• Strong documentation discipline and attention to detail
• Comfortable working onsite in a fast‑paced manufacturing environment