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Sr Validation Engineer Jobs in Ohio (NOW HIRING)

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

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 ...

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

Columbus, 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

Columbus, 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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Sr Validation Engineer information

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$61

$93

How much do sr validation engineer jobs pay per hour?

As of Aug 26, 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?

For Sr Validation Engineer jobs in Ohio, the most frequently searched job titles are:

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

The top searched job categories for Sr Validation Engineer jobs in Ohio are:

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

Cities in Ohio with the most Sr Validation Engineer job openings:

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 87% Full Time, 7% Part Time, and 6% Contract. Highlights an 82% Physical, 5% Hybrid, and 13% Remote job distribution, with an average salary of $128,084 per year, or $61.6 per hour.

Veeva LIMS SME Consultant / Senior Validation Engineer

Spadtek Solutions LLC

Columbus, OH • On-site

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Title : Veeva LIMS SME Consultant / Senior Validation Engineer

Location: Columbus, OH – Onsite

Job Description:

We are seeking an experienced Veeva LIMS SME Consultant / Senior Validation Engineer to support a Veeva LIMS implementation and validation activities within a GxP-regulated environment.

The ideal candidate will have strong hands-on experience with Veeva LIMS, Computer System Validation (CSV)/Computer Software Assurance (CSA), and pharmaceutical/biotechnology validation practices.

Responsibilities:

  • Lead/support Veeva LIMS implementation and validation activities throughout the system lifecycle, from requirements and design through testing, deployment, and validation closeout.

  • Develop and/or review validation deliverables including URS, risk assessments, validation plans, test scripts, traceability matrices, validation summary reports, and SOPs.

  • Partner with Quality, Laboratory, IT, Business Process Owners, and system stakeholders to define requirements and ensure compliance with business and regulatory needs.

  • Support Veeva LIMS configuration, functional testing, integration testing, UAT, and defect resolution.

  • Apply risk-based CSV/CSA principles and applicable GxP requirements to maintain the validated state of the system.

  • Support data migration, interfaces, integrations, and related systems as part of the LIMS implementation.

  • Participate in change control, deviations, CAPAs, periodic reviews, and other system lifecycle activities.

  • Provide technical and validation expertise during implementation meetings, workshops, testing activities, and issue resolution.

  • Ensure compliance with GAMP 5, 21 CFR Part 11, EU Annex 11, and data integrity principles.

  • Support inspection and audit readiness by ensuring complete, accurate, and traceable validation documentation.

Required Qualifications:

  • Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related technical discipline.

  • 5+ years of experience in CSV, CSA, quality, or validation engineering within pharmaceutical, biotechnology, or other GxP-regulated environments.

  • Hands-on Veeva LIMS implementation, validation, or lifecycle management experience is required.

  • Strong understanding of CSV/CSA methodologies, GxP requirements, risk-based validation, and data integrity.

  • Experience developing and executing validation/testing documentation.

  • Strong knowledge of 21 CFR Part 11, EU Annex 11, and GAMP 5.

  • Strong project management, organizational, communication, and problem-solving skills.

  • Must be willing to work onsite in Columbus, OH.

Apply