1

Validation Jobs in Ohio (NOW HIRING)

Validation Specialists develop and execute C&Q protocols (e.g., IQ/OQ/PQ) for these industries. Protocols may include verification of manufacturing / packaging facilities, process and packaging ...

Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential ...

Validation Engineer

Columbus, OH ยท On-site

$72K - $80K/yr

Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential ...

Validation Engineer

Columbus, OH ยท On-site

$72K - $80K/yr

Are You Ready? CAI is a professional services company established in 1996 that has grown to nearly 800 people worldwide. For mission-critical and regulated industries needing to deliver essential ...

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...

Senior Validation Engineer

Cincinnati, OH ยท On-site

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...

Showing results 21-40

Validation information

See Ohio salary details

$21

$49

$74

How much do validation jobs pay per hour?

As of Aug 3, 2026, the average hourly pay for validation in Ohio is $49.43, according to ZipRecruiter salary data. Most workers in this role earn between $37.50 and $60.10 per hour, depending on experience, location, and employer.

What is the difference between Validation vs Quality Assurance?

AspectValidationQuality Assurance
PurposeEnsures products meet specifications and intended usePrevents defects through process improvements
FocusProduct-specific testing and verificationProcess and system quality control
ActivitiesDesign validation, process validation, equipment validationAudits, process reviews, standards compliance
TimingBefore product releaseThroughout production cycle

Validation focuses on confirming that a product or process meets specified requirements before release, while Quality Assurance emphasizes maintaining quality standards throughout the production process to prevent defects. Both roles are essential in industries like pharmaceuticals and manufacturing, but they serve different stages of quality management.

What are the key skills and qualifications needed to thrive as a validation engineer, and why are they important?

To thrive as a Validation Engineer, you need a solid background in engineering or life sciences, with expertise in quality assurance and regulatory compliance. Familiarity with validation protocols, statistical analysis tools, and industry standards such as GMP, FDA, or ISO guidelines is essential. Strong analytical thinking, attention to detail, and effective communication skills help you identify issues and collaborate across teams. These abilities ensure that products and processes meet strict safety and quality requirements, minimizing risks and ensuring regulatory approval.

What are some common challenges faced by professionals in validation roles, and how can they be overcome?

Professionals in validation roles often face challenges such as tight project timelines, evolving regulatory requirements, and the need for meticulous documentation. Balancing thoroughness with efficiency is crucial, as validation processes must be both comprehensive and timely to support product launches or regulatory submissions. Effective communication with cross-functional teams, proactive planning, and staying updated with industry standards can help overcome these challenges and ensure successful validation outcomes.

What is a validation job?

Validation jobs involve ensuring that products, processes, or systems meet specific requirements and function as intended. In industries like pharmaceuticals, biotechnology, and manufacturing, validation specialists test equipment, procedures, and software to guarantee quality and compliance with regulatory standards. These professionals document their findings and help identify areas for improvement, playing a key role in quality assurance. Validation jobs are essential for maintaining product safety, effectiveness, and meeting industry regulations.
What are the most commonly searched types of Validation jobs in Ohio? The most popular types of Validation jobs in Ohio are:
What cities in Ohio are hiring for Validation jobs? Cities in Ohio with the most Validation job openings:
Infographic showing various Validation job openings in Ohio as of July 2026, with employment types broken down into 79% Full Time, 5% Part Time, and 16% Contract. Highlights an 95% In-person, and 5% Hybrid job distribution, with an average salary of $102,820 per year, or $49.4 per hour.

Field Validation Engineer

Rees Scientific Corporati

Cleveland, OH โ€ข On-site

Full-time

Re-posted 13 days ago


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