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Field Validation Engineer

Rees Scientific Corporati
Posted 4 months ago, valid for 13 days
Location

St. Louis, MO, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The Field Validation Engineer at Rees Scientific is tasked with executing validation and qualification activities for environmental monitoring systems in regulated environments.
  • Candidates should possess a Bachelor's degree in Engineering or have five to seven years of validation experience in relevant fields.
  • The role focuses on technical execution, compliance, and customer satisfaction without people-management responsibilities.
  • The position requires strong technical skills in validation lifecycle processes and familiarity with GMP, FDA regulations, and documentation standards.
  • Salary details are not provided, but the role demands extensive travel and physical capability to perform field validation activities.

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






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