Validation Specialist

    Highlights

    The contractor will be responsible for executing qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), for manufacturing equipment, processes, and materials within a regulated manufacturing environment. Job Summary: We are seeking a hands-on Equipment Qualification & Process Validation Contractor to support the Enterprise Quality Change Management & Systems organization.

    Numbers & Facts

    LocationRichmond, VA

    Description

    Job Summary:
    • We are seeking a hands-on Equipment Qualification & Process Validation Contractor to support the Enterprise Quality Change Management & Systems organization.
    • The contractor will be responsible for executing qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ), for manufacturing equipment, processes, and materials within a regulated manufacturing environment.
    • This is an execution-focused role, with day-to-day direction from the Manager.
    • Success will be measured by the timely, accurate, and right-first-time completion of qualification deliverables.

    Responsibilities:

    • Execute and close IQ/OQ/PQ protocols for manufacturing equipment and systems.
    • Author protocols, qualification reports, and GMP-compliant documentation.
    • Document deviations/discrepancies and maintain full record traceability.
    • Coordinate qualification activities with Manufacturing, Engineering, Quality, and Project teams.
    • Support change control, documentation remediation, and record management.
    • Execute qualification activities on the factory floor around production schedules.

    Qualifications:

    • Bachelor's degree in a technical discipline or equivalent experience.
    • 5+ years of hands-on IQ/OQ/PQ and process validation experience in GMP or regulated manufacturing.
    • Experience with protocol writing, execution, reports, deviations, and traceability.
    • Proficiency with eQMS (TrackWise or similar), document management systems, and MS Office/Excel.
    • CQE, CQA, ASQ, or similar certification preferred.

    Top 3 Skills:

    • IQ/OQ/PQ & Process Validation.
    • Technical Writing & GMP Documentation.
    • Cross-Functional Coordination & Factory-Floor Execution.

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