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Validation Engineer Jobs in Ohio (NOW HIRING)

CAI

Senior Validation Engineer

Cincinnati, OH

$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

Senior Validation Engineer

Cincinnati, OH · On-site

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

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How much do validation engineer jobs pay per hour?

As of Jun 12, 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.

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.

What are Validation Engineers?

Validation Engineers are professionals responsible for ensuring that systems, processes, or equipment meet regulatory standards and function as intended. They typically work in industries such as pharmaceuticals, biotechnology, manufacturing, and medical devices. Their duties involve creating validation protocols, conducting tests, analyzing data, and documenting results to ensure compliance with industry regulations and quality standards. Validation Engineers play a critical role in maintaining product safety and efficacy, as well as helping companies pass audits and inspections.
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 June 2026, with employment types broken down into 94% Full Time, 3% Part Time, and 3% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $102,820 per year, or $49.4 per hour.
SeniorPackaging Validation Engineer, Biotech GMP Final Drug Product (JP14454)

SeniorPackaging Validation Engineer, Biotech GMP Final Drug Product (JP14454)

3 Key Consulting

New Albany, OH • On-site

$53 - $63/hr

Other

Posted 17 days ago

Job description

Job Title:SeniorPackaging Validation Engineer, Biotech GMP Final Drug Product (JP14454)
Location:New Albany, Oh 43054
Business Unit: Site Process Development
Employment Type: Contract
Duration:2+ years with possible extension or conversion to FTE
Rate: $53 - $63/hour (DOE) - W2 with benefits
Posting Date: 8/28/2025.
3 Key Consulting is hiring! We are recruiting aSeniorValidation Engineerfor a consulting engagement with our direct client, a leading global biotechnology company.
The Senior Validation Engineer position reports into the Sr. Manager of Validation. This position requires the application of diverse and advanced engineering and scientific principles in support of commercial GMP Final Drug Product (FDP) operations.
Location Options: 100% Site Presence Required. The position is expected to travel for approximately 10%.
Job Description & Responsibilities:
The Senior Validation Engineering will support the development and implementation of automated and semi-automated combination product assembly equipment initiatives as part of the Finished Drug Product (FDP) product portfolio at the Ohio manufacturing site. The position is a key role in the Process Development team where the candidate must manage and/or apply extensive technical expertise (characterization, validation and troubleshooting) in the validation of combination products. This position also requires the application of advance and diverse engineering principles to more than one area of engineering (process, unit operations, equipment, devices and materials) in complex process optimization, scale up and manufacturing support projects.
Output:
Key responsibilities will include supporting the packaging C&Q activities of the product portfolio to AOH. Additional responsibilities will include the provision of technical operations support for the continuous improvement of device assembly and packaging line capacity and performance, and advisory of technical improvement projects. The Sr. Validation Engineer must ensure effective communication throughout the Ohio commercial site and network with all stakeholders and deliver on technical deliverables.
Relationship:
The Senior Validation Engineering is expected to build on the network expertise across the company commercial and clinical operations for product assembly, label and packaging. The position is expected to leverage this network in support of GMP technical expertise, performance trending, equipment standardization and troubleshooting/process
The successful candidate will have:
  • Knowledge of high-speed, highly automated secondary packaging operations
  • Knowledge of the validation of equipment such as PFS assembly, cartoners, vision systems
  • Experience in writing protocols
  • Experience in executing protocols
  • Capable of executing multiple projects
  • Communication skills and ability to work with other people
  • Bring innovative solutions for continuous process improvement
  • Experience with Kneat
  • Experience with MiniTab is a plus
Top Must Have Skill Sets:
  • packaging validation experience
  • knowledge of packaging equipment
  • protocol generation and execution
Day to Day Responsibilities:
  • writing and executing validation protocols.

Value proposition: Unique industry opportunity Networking
Basic Qualifications:
Doctorate degree OR Masters degree and 2 years of experience OR Bachelors degree and 4 years of experience OR Associates degree and 8 years of experience
Why is the Position Open?
Supplement additional workload on team
Interview Process:
Initial screening with hiring manager
Final interview panel with 3 interviewers
We invite qualified candidates to sendyour resume torecruiting@3keyconsulting.com. Ifyou decide that you're not interested in pursuing this particular position, please feel free to take a look at the other positions on our websitewww.3keyconsulting.com/careers. You are also welcome to sharethis opportunity withanyone you think might be interested in applying for this role.

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