Validation Engineer - Vista - Barrington James

    Barrington James
    Barrington James Vista

    2 days ago

    Pharmaceutical / Bio-tech
    Description

    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

    • 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

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