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Sr 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

$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 ...

RadNet, Inc.

$120 - $180/hr

As a Senior ASIC Post-Silicon Validation Engineer, you will help validate and characterize key technologies that enable the next generation of semiconductor testing. Therefore, you develop and align ...

New

Deloitte

System Test and Validation Lead

Cleveland, OH · On-site +1

Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

Deloitte

System Test and Validation Lead

Cleveland, OH · On-site +1

Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

Deloitte

System Test and Validation Lead

Dayton, OH · On-site +1

Work you'll do As a Senior Consultant, Regulatory, Risk, and Compliance on the Regulatory, Risk ... Bachelor's degree in business, information systems, computer science, engineering, or equivalent ...

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All JobsSr Validation Engineer JobsSr Validation Engineer Jobs in Ohio

Sr Validation Engineer information

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$33

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$93

How much do sr validation engineer jobs pay per hour?

As of Aug 21, 2026, the average hourly pay for sr validation engineer in Ohio is $61.58, according to ZipRecruiter salary data. Most workers in this role earn between $49.13 and $69.95 per hour, depending on experience, location, and employer.

What is a Sr validation engineer?

Sr Validation Engineers are experienced professionals responsible for ensuring that products, systems, or processes meet regulatory standards and function as intended. They lead validation projects, develop protocols, oversee testing, and document results to confirm compliance with industry regulations, such as those from the FDA or ISO. Their work is essential in industries like pharmaceuticals, biotechnology, and manufacturing, where product quality and safety are critical. Senior validation engineers also mentor junior staff and help improve validation processes within their organizations.

What are the key skills and qualifications needed to thrive as a Sr validation engineer?

To thrive as a Sr Validation Engineer, you need a solid background in engineering or life sciences, extensive experience with validation protocols, and a strong understanding of regulatory standards such as FDA, GMP, or ISO. Expertise in using validation software, risk assessment tools, and familiarity with documentation management systems is typically required, along with certifications like Six Sigma or ASQ CQE being advantageous. Exceptional problem-solving abilities, attention to detail, and effective communication skills help you lead teams and interact with cross-functional departments. These competencies are crucial for ensuring products and processes meet compliance standards, maintain quality, and support organizational success.

What are some common challenges a Sr validation engineer faces when managing multiple validation projects simultaneously?

A Sr Validation Engineer often manages several validation projects at once, which can present challenges such as coordinating timelines, ensuring compliance with regulatory standards, and balancing cross-functional communication. Keeping detailed documentation and staying organized are essential, as unexpected equipment issues or shifting project priorities may arise. Successful engineers proactively communicate with quality, manufacturing, and R&D teams to mitigate risks, maintain project momentum, and deliver results within required deadlines.

What is the difference between Sr Validation Engineer vs Validation Engineer?

AspectSr Validation EngineerValidation Engineer
Required CredentialsBachelor's/Master's in Engineering, certifications like CQE or ASQ, experience in validation processesBachelor's in Engineering or related field, some certifications preferred, less experience required
Work EnvironmentPharmaceutical, biotech, or manufacturing industries; leading validation projectsSupporting validation tasks under supervision, often in similar industries
Employer & Industry UsageUsed by companies requiring compliance with FDA, ISO, or GMP standardsCommonly used in manufacturing and quality assurance roles

The main difference between a Sr Validation Engineer and a Validation Engineer lies in experience, responsibility, and expertise. The Sr Validation Engineer typically leads validation projects, has more advanced certifications, and plays a strategic role in compliance. Validation Engineers support validation activities and often work under supervision. Both roles are essential in regulated industries like pharmaceuticals and manufacturing, but the senior role involves greater leadership and technical oversight.

What are popular job titles related to Sr Validation Engineer jobs in Ohio?

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What job categories do people searching Sr Validation Engineer jobs in Ohio look for?

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What cities in Ohio are hiring for Sr Validation Engineer jobs?

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Sr Validation Engineer jobs near you
Infographic showing various Sr Validation Engineer job openings in Ohio as of August 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $128,084 per year, or $61.6 per hour.

Senior Packaging Validation Engineer, Biotech GMP Final Drug Product

3 Key Consulting

New Albany, OH • On-site

$100K - $137K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Senior Validation Engineer, Biotech GMP Final Drug Product3 Key Consulting is hiring! We are recruiting a Senior Validation Engineer for 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 & ResponsibilitiesThe 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.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.RelationshipThe 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 operationsKnowledge of the validation of equipment such as PFS assembly, cartoners, vision systemsExperience in writing protocolsExperience in executing protocolsCapable of executing multiple projectsCommunication skills and ability to work with other peopleBring innovative solutions for continuous process improvementExperience with KneatExperience with MiniTab is a plusTop Must Have Skill Sets:Packaging validation experienceKnowledge of packaging equipmentProtocol generation and executionDay to Day Responsibilities:Writing and executing validation protocols.Value proposition: Unique industry opportunity NetworkingBasic 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 experienceWhy is the Position Open? Supplement additional workload on teamInterview Process: Initial screening with hiring manager Final interview panel with 3 interviewers

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