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Validation Engineer Jobs in Ohio (NOW HIRING)

CAI

Entry Level Validation Engineer

Columbus, OH

$60K - $70K/yr

... or engineering field preferred but not required - 0- 2 years work experience in any industry - Familiarity with ISPE Baseline Guide 5 (Second Edition) is a plus - Preferred experience in ...

CAI

Senior Validation Engineer

Cincinnati, OH · On-site

$87K - $94K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Entry Level Validation Engineer

Columbus, OH · On-site

$60K - $70K/yr

  • Medical

  • Life

  • PTO

... or engineering field preferred but not required - 0- 2 years work experience in any industry - Familiarity with ISPE Baseline Guide 5 (Second Edition) is a plus - Preferred experience in ...

CAI

Entry Level Validation Engineer

Columbus, OH · On-site

$60K - $70K/yr

  • Medical

  • Life

  • PTO

... or engineering field preferred but not required - 0- 2 years work experience in any industry - Familiarity with ISPE Baseline Guide 5 (Second Edition) is a plus - Preferred experience in ...

CAI

Senior Validation Engineer

Cincinnati, OH · On-site

$87K - $94K/yr

  • Medical

  • Life

  • PTO

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

Trimble

Systems & Firmware Validation Engineer

Dayton, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Systems & Firmware Validation Engineer Location: Dayton, OH (In-Office) Division: CTCT Lead Our Next Breakthrough as a Systems & Firmware Validation Engineer! Ready to bridge the gap between advanced ...

Trimble, Inc.

Systems & Firmware Validation Engineer

Dayton, OH · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Systems & Firmware Validation Engineer Location: Dayton, OH (In-Office) Division: CTCT Lead Our Next Breakthrough as a Systems & Firmware Validation Engineer! Ready to bridge the gap between advanced ...

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All JobsValidation Engineer JobsValidation Engineer Jobs in Ohio

Validation Engineer information

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How much do validation engineer jobs pay per hour?

As of Aug 13, 2026, the average hourly pay for validation engineer 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.

Is validation engineer a good job?

Validation engineers are responsible for ensuring that products and processes meet quality standards through testing and documentation, often working in industries like pharmaceuticals, biotech, or manufacturing. The role typically requires knowledge of regulatory requirements, validation protocols, and tools like GxP or SOPs, and can offer stable employment with opportunities for advancement. Job satisfaction depends on individual interests in quality assurance, technical skills, and industry stability.

What degree do you need to be a validation engineer?

Validation engineers typically hold a bachelor's degree in engineering, life sciences, or a related field. Some roles may require a master's degree or specialized certifications in quality assurance or validation processes. Strong knowledge of regulatory standards and experience with validation tools are also important.

What is a validation engineer?

A validation engineer is responsible for testing equipment and electrical systems used in the manufacturing process. As a validation engineer, your primary duty is to work with the other members of the validation team to ensure that these systems measure up to company and industry standards. Skills needed for a validation engineer job include the ability to accurately test, measure, and calibrate manufacturing equipment for maximum efficiency and quality.

What is the difference between Validation Engineer vs Quality Assurance Engineer?

AspectValidation EngineerQuality Assurance Engineer
CertificationsGMP, ISO, Six SigmaISO, Six Sigma, CQA
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, and product development
Primary FocusEnsuring products meet specifications through validation processesPreventing defects through process and system improvements
Common UsageRegulatory compliance, validation protocolsProcess audits, quality systems

Validation Engineers focus on verifying that products and processes meet regulatory standards through validation protocols, especially in regulated industries. Quality Assurance Engineers concentrate on maintaining overall product quality by implementing and auditing quality systems. While both roles aim to ensure product safety and efficacy, Validation Engineers are more involved in validation activities, whereas QA Engineers focus on process improvement and defect prevention.

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, quality assurance, and regulatory compliance, typically backed by a degree in engineering or a related field. Familiarity with validation protocols, statistical analysis tools, and industry-specific regulations such as FDA, GMP, or ISO standards is essential. Strong analytical thinking, attention to detail, and effective communication set top performers apart in this role. These skills ensure that products and processes meet stringent quality and safety standards, minimizing risks and ensuring regulatory approval.

What are some common challenges validation engineers face when working cross-functionally with other departments?

Validation Engineers frequently collaborate with teams such as manufacturing, quality assurance, and research & development. One common challenge is aligning differing priorities and timelines between departments, which can sometimes delay validation projects. Effective communication skills and flexibility are crucial to navigating these cross-functional interactions, ensuring that all regulatory and quality requirements are met without hindering production schedules. Building strong working relationships and proactively addressing potential concerns can help Validation Engineers facilitate smoother project execution.
More about Validation Engineer jobs
What are the most commonly searched types of Validation Engineer jobs in Ohio? The most popular types of Validation Engineer jobs in Ohio are:
What are popular job titles related to Validation Engineer jobs in Ohio? For Validation Engineer jobs in Ohio, the most frequently searched job titles are:
What job categories do people searching Validation Engineer jobs in Ohio look for? The top searched job categories for Validation Engineer jobs in Ohio are:
What cities in Ohio are hiring for Validation Engineer jobs? Cities in Ohio with the most Validation Engineer job openings:
What are popular job titles related to Validation Engineer jobs in OH? For Validation Engineer jobs in OH, the most frequently searched job titles are:
Validation Engineer jobs near you
Infographic showing various Validation Engineer job openings in Ohio as of August 2026, with employment types broken down into 90% Full Time, 2% Part Time, and 8% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $102,820 per year, or $49.4 per hour.

Mechanical Product Validation Engineer

Belcan

Cincinnati, OH • On-site

$50 - $60/hr

Contractor

Posted 3 days ago

New

Job description


Job Title: Mechanical Product Validation Engineer
Pay Rate: $50-60/hr
Duration: 24-month contract
Location: Cincinnati, OH
Zip Code: 45242
Start Date: Right Away
Keywords: #ValidationEngineerJobs
Summary:
Mechanical Product Validation Engineer with 5-10 years of experience in the medical device industry, specializing in cleaning, sterilization, and reprocessing validation for reusable medical devices. Responsible for planning and executing cleaning and sterilization feasibility studies, validation activities, test method development, and GR&R studies to ensure product safety, compliance, and performance. Experienced in root cause analysis, risk management (DFMEA/PFMEA), statistical data analysis, and technical documentation. Proven ability to collaborate with R&D, Quality, Regulatory, and external partners to support product development, design reviews, and successful product launches in a regulated environment.
Responsibilities:
* Develop soiling, cleaning and extraction processes for reusable scopes and instruments and accessories (I&A), incorporating real world use conditions and cleanability considerations.
* Plan, execute and analyze Cleaning and Sterilization (C&S) feasibility studies, cleanability assessments and sterilization validations for reusable scopes and I&A.
* Create and qualify test methods, perform Gage Repeatability & Reproducibility (GR&R) studies and document results in engineering studies, test protocols, reports and validation documentation, including statistical analysis as required.
* Conduct root cause analysis for C&S process issues and evaluation findings and communicate data driven solutions and recommendations to R&D and cross functional stakeholders.
* Support development and completion of associated risk management documentation (e.g., DFMEA, PFMEA, hazard analyses) by providing hands on laboratory expertise and technical input.
* Support Design Reviews and Phase Exit Reviews by preparing required documentation, developing presentation materials and presenting technical content related to cleaning, sterilization and reprocessing.
* Partner with internal teams and external supplier resources (e.g., test laboratories, sterilization vendors) to ensure timely completion of product development and launch deliverables.
Required Qualifications:
* B.E./B.Tech in Mechanical Engineering or equivalent with 5+ years of experience in the medical device industry.
* Hands-on expertise in cleaning, sterilization, and reprocessing validation for reusable medical devices.
* Proven experience in developing and validating cleaning and sterilization test methods, including feasibility studies and validation protocols.
* Strong knowledge of validation methodologies, including GR&R studies, root cause analysis, and statistical data evaluation.
* Experience supporting risk management activities, design reviews, and cross-functional project teams throughout the product development lifecycle.
* Familiarity with applicable regulatory and industry standards for reusable medical devices, including validation and documentation requirements.
* Strong technical writing, problem-solving, and communication skills with the ability to collaborate effectively across engineering, quality, and regulatory functions.
Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, color, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.
Minimum Security Clearance
NONE
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About Belcan

Sourced by ZipRecruiter

Belcan is a leading provider of qualified personnel to many of the world's most respected enterprises. We offer excellent opportunities for contract/temporary, temp-to-hire, and direct assignments in the engineering, IT, and professional fields. We are the employer of choice for thousands worldwide. Our overriding goal is to provide quality staffing solutions that help people, organizations, and communities succeed.

Industry

It services

Company size

5,001 - 10,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1958

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