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Field Validation Engineer

Rees Scientific Corporati
  • Cleveland, OH
    Today

    Job Description

    Job Description

    Job Description

    CLEVELAND, OHIO

    Job Summary:


    The Field Validation Engineer at Rees Scientific is responsible for executing validation and qualification activities for environmental monitoring systems and customer equipment in regulated environments. This role supports installation, validation, calibration, and system verification while ensuring all activities meet established operational, quality, and regulatory standards.

    The Field Validation Engineer serves as a technical resource in the field, supporting validation lifecycle activities including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ). This position does not include people-management responsibilities and is focused on technical execution, compliance, and customer satisfaction.

    Working closely with Field Service leadership, Technical Support, Engineering, Quality, and Project teams, the Field Validation Engineer plays a critical role in ensuring accurate, compliant, and efficient validation delivery across assigned regions.


    Key Responsibilities:


    Field Validation Execution & Technical Support
    • Perform validation activities including IQ, OQ, and PQ for Rees Scientific systems and customer equipment
    • Execute temperature mapping, calibration verification, and environmental monitoring system validation
    • Support computer system validation (CSV) activities in alignment with GAMP and data integrity standards
    • Troubleshoot and resolve validation-related and system performance issues in the field
    • Verify system configuration, functionality, and compliance with technical specifications and regulatory requirements
    • Review validation protocols and job documentation prior to execution and provide required updates


    Quality, Documentation & Compliance

    • Develop, execute, and complete validation documentation including protocols, reports, and supporting records
    • Ensure all validation activities comply with GMP, GLP, FDA, ISO, and customer-specific requirements
    • Support investigations, deviations, CAPAs, and change control activities as required
    • Maintain audit-ready documentation and validation records in accordance with company and regulatory standards


    Customer Support & Collaboration

    • Communicate effectively with customers regarding validation activities, system performance, and compliance requirements
    • Support customer escalations and validation-related technical inquiries
    • Collaborate with internal teams including Engineering, Technical Support, Quality, and Program Management
    • Provide guidance to field service personnel on validation-related activities when needed


    Continuous Improvement & Training

    • Maintain current knowledge of validation practices, regulatory requirements, and Rees Scientific systems
    • Participate in required training and certification programs
    • Provide feedback to Field Service leadership regarding validation processes, tools, and service improvements

    Qualifications & Experience

    • Bachelor’s degree from a four-year college or university in Engineering (Electrical, Mechanical, Biomedical, Chemical, or related discipline) preferred; or
    • Five to seven years of validation experience in pharmaceutical, biotechnology, or regulated manufacturing environments; or
    • Equivalent combination of education and experience
    • Strong technical background in validation lifecycle (IQ/OQ/PQ), CSV, and temperature mapping
    • Experience with GMP, FDA regulations, GAMP, and data integrity requirements
    • Strong technical writing skills for validation documentation (protocols, reports, SOPs)
    • Ability to work independently with minimal supervision
    • Strong organizational, documentation, and communication skills

    Physical Requirements:

    • Ability to travel extensively within assigned regions, including overnight and extended travel
    • Ability to lift and carry up to 50 pounds
    • Ability to stand, walk, bend, reach, kneel, and climb ladders as required
    • Comfortable working in laboratories, cleanrooms, and industrial environments, including temperature variations
    • Ability to follow all safety protocols and procedures while performing field validation activities


    Numbers & Facts

    LocationCleveland, OH
    IndustryElectronics, Components, and Semiconductor Mfg
    Company Size50 to 99 employees
    Year Founded1982
    Websitehttp://www.reesscientific.com/

    About Company

    Rees Scientific provides automated environmental monitoring to a limitless number of applications in a wide range of industries. From Pharmaceutical to Blood Banking, Laboratory Animal Research to Biotech and Hospitals, Rees Scientific has become the standard by which other monitoring systems are judged. Our Centron Monitoring System monitors critical parameters such as temperature, humidity, differential pressure, lighting control, carbon dioxide, oxygen, light and air changes per hour. It monitors critical equipment such as stability chambers, refrigerators, freezers, LN2 Tanks, incubators, animal holding rooms, ultra-low freezers, cold rooms and clean rooms.

    As an ISO 9001:2008 Company, Rees Scientific is constantly upgrading policies, procedures, and protocols to comply with today’s highly regulated environments. Rees is the only known monitoring company with a dedicated sales staff of our size located within the United States offering prompt site visits and the ability to address needs promptly. We also offer a full array of validation, calibration and training to fit each clients specific needs and requirements. We employ over 50 regionalized field service technicians throughout the U.S.; most are armed with well-stocked vans to handle your service needs immediately. Lastly, regardless of where you are located, our live 24/7/365 technical support team ensures requests are responded to promptly and closed out correctly.

    Skills

    • Biomedicineunmatched
    • Biotech and Pharmaceuticalunmatched
    • Calibrationunmatched
    • Change Controlunmatched
    • Cleanroomunmatched
    • Communication Skillsunmatched
    • Computer Systemsunmatched
    • Customer Escalationsunmatched
    • Customer Satisfactionunmatched
    • Customer Support/Serviceunmatched
    • Data Qualityunmatched
    • Documentationunmatched
    • Electrical Engineeringunmatched
    • Environmental Monitoringunmatched
    • FDA (Food and Drug Administration)unmatched
    • FDA Requirementsunmatched
    • Field Trialsunmatched
    • GLP (Good Laboratory Practices)unmatched
    • GMP (Good Manufacturing Practices)unmatched
    • ISO (International Organization for Standardization)unmatched
    • Identify Issuesunmatched
    • Laboratoryunmatched
    • Leadershipunmatched
    • Lift/Move 50 Poundsunmatched
    • Manufacturingunmatched
    • On Site Supportunmatched
    • Organizational Skillsunmatched
    • People Managementunmatched
    • Process Validationunmatched
    • Project/Program Managementunmatched
    • Quality Managementunmatched
    • Regulationsunmatched
    • Regulatory Complianceunmatched
    • Regulatory Requirementsunmatched
    • Safety Processunmatched
    • Standard Operating Procedures (SOP)unmatched
    • System Validationunmatched
    • Systems Administration/Managementunmatched
    • Technical Supportunmatched
    • Technical Writingunmatched
    • Temperature Mappingunmatched
    • Training Programunmatched
    • Validation Documentationunmatched
    • Validation Planunmatched
    • Willing to Travelunmatched
    • Writing Skillsunmatched

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