Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the ...
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Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the ...
Validation Engineer
$100K - $160K/yr
Your Role The Validation Engineer supports system validation activities within regulated manufacturing environments. The role works closely with cross-functional teams to ensure automation software ...
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Validation Engineer
$100K - $160K/yr
Your Role The Validation Engineer supports system validation activities within regulated manufacturing environments. The role works closely with cross-functional teams to ensure automation software ...
Validation Engineer
Columbus, OH · On-site
Your Role The Validation Engineer supports system validation activities within regulated manufacturing environments. The role works closely with cross-functional teams to ensure automation software ...
Validation Engineer
Columbus, OH · On-site
Your Role The Validation Engineer supports system validation activities within regulated manufacturing environments. The role works closely with cross-functional teams to ensure automation software ...
Your Role The Validation Engineer supports system validation activities within regulated manufacturing environments. The role works closely with cross-functional teams to ensure automation software ...
Your Role The Validation Engineer supports system validation activities within regulated manufacturing environments. The role works closely with cross-functional teams to ensure automation software ...
Validation Engineer
Columbus, OH · On-site
$72K - $80K/yr
... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and qualification in a regulated industry - Familiarity with ISPE Baseline Guide 5 (Second Edition) is a plus ...
Validation Engineer
Columbus, OH · On-site
$72K - $80K/yr
... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and qualification in a regulated industry - Familiarity with ISPE Baseline Guide 5 (Second Edition) is a plus ...
Validation Engineer
$72K - $80K/yr
... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and qualification in a regulated industry - Familiarity with ISPE Baseline Guide 5 (Second Edition) is a plus ...
Quick apply
Validation Engineer
$72K - $80K/yr
... engineering field (or equivalent experience) - 2-4 years' experience in commissioning and qualification in a regulated industry - Familiarity with ISPE Baseline Guide 5 (Second Edition) is a plus ...
A Brief Overview The Validation Engineer is responsible for planning, executing, and documenting validation activities to ensure compliance with cGMP regulations and company quality standards. This ...
A Brief Overview The Validation Engineer is responsible for planning, executing, and documenting validation activities to ensure compliance with cGMP regulations and company quality standards. This ...
Engineer, Validation
New Albany, OH · On-site
A Brief Overview The Validation Engineer is responsible for planning, executing, and documenting validation activities to ensure compliance with cGMP regulations and company quality standards. This ...
Engineer, Validation
New Albany, OH · On-site
A Brief Overview The Validation Engineer is responsible for planning, executing, and documenting validation activities to ensure compliance with cGMP regulations and company quality standards. This ...
I am working on C&Q Validation Engineer position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed is as follows Role: C&Q ...
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I am working on C&Q Validation Engineer position right now. Please send me your updated resume if you have relevant experience and interested in this position. The detailed is as follows Role: C&Q ...
C&Q Engineer (Commissioning & Qualification Engineer) Columbus, OH Project Duration: 6-9+ Months Job Summary: We are looking for an experienced Commissioning & Qualification (C&Q) Engineer to support ...
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C&Q Engineer (Commissioning & Qualification Engineer) Columbus, OH Project Duration: 6-9+ Months Job Summary: We are looking for an experienced Commissioning & Qualification (C&Q) Engineer to support ...
Test Method Validation
Delaware, OH · On-site
Coach and mentor validation engineers to ensure proper execution of test protocols and adherence to validation best practices. Review and support development of TMV protocols, test methods, and ...
New
Test Method Validation
Delaware, OH · On-site
Coach and mentor validation engineers to ensure proper execution of test protocols and adherence to validation best practices. Review and support development of TMV protocols, test methods, and ...
New
Engineering Validation Supervisor
Hebron, OH · On-site
Lead and manage the testing, development, validation, and sign off of all major product programs ... Minimum Qualifications * 7+ years' experience as a test engineer working with hydraulic, pneumatic ...
Engineering Validation Supervisor
Hebron, OH · On-site
Lead and manage the testing, development, validation, and sign off of all major product programs ... Minimum Qualifications * 7+ years' experience as a test engineer working with hydraulic, pneumatic ...
Job Title: Sr. Engineer, Cleaning Validation Location: Columbus, OH Job Type: Full time Req ID: 10915 About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma ...
Job Title: Sr. Engineer, Cleaning Validation Location: Columbus, OH Job Type: Full time Req ID: 10915 About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma ...
Job Title: Sr. Engineer, Cleaning Validation Location: Columbus, OH Job Type: Full time Req ID: 10915 About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma ...
Job Title: Sr. Engineer, Cleaning Validation Location: Columbus, OH Job Type: Full time Req ID: 10915 About Us: As a developer, manufacturer, and supplier of essential medicines, Hikma ...
CQV Engineer
$45 - $55/hr
CQV Engineers are responsible for the commissioning, qualification, and validation for facilities, utilities, and equipment in the pharmaceutical and biotech industries. Our engineers play a critical ...
Quick apply
CQV Engineer
$45 - $55/hr
CQV Engineers are responsible for the commissioning, qualification, and validation for facilities, utilities, and equipment in the pharmaceutical and biotech industries. Our engineers play a critical ...
CQV Engineers are responsible for the commissioning, qualification, and validation for facilities, utilities, and equipment in the pharmaceutical and biotech industries. Our engineers play a critical ...
CQV Engineers are responsible for the commissioning, qualification, and validation for facilities, utilities, and equipment in the pharmaceutical and biotech industries. Our engineers play a critical ...
CQV Engineer (New Grad)
Columbus, OH · On-site
Understanding validation documents, URS, IQ, OQ, PQ Requirements * Must be willing to work onsite in Columbus, OH * Bachelor's Degree or equivalent required (STEM degree highly preferred)
CQV Engineer (New Grad)
Columbus, OH · On-site
Understanding validation documents, URS, IQ, OQ, PQ Requirements * Must be willing to work onsite in Columbus, OH * Bachelor's Degree or equivalent required (STEM degree highly preferred)
This position bridges product validation and application engineering by overseeing system-level testing, first-of-kind validation efforts with customers and partners, and cross-functional integration ...
This position bridges product validation and application engineering by overseeing system-level testing, first-of-kind validation efforts with customers and partners, and cross-functional integration ...
This position bridges product validation and application engineering by overseeing system-level testing, first-of-kind validation efforts with customers and partners, and cross-functional integration ...
This position bridges product validation and application engineering by overseeing system-level testing, first-of-kind validation efforts with customers and partners, and cross-functional integration ...
CQV Engineer
Columbus, OH · On-site
CQV Engineers are responsible for thecommissioning,qualification, and validation for facilities,utilities, andequipment in the pharmaceutical and biotechindustries. Ourengineers play a critical role ...
CQV Engineer
Columbus, OH · On-site
CQV Engineers are responsible for thecommissioning,qualification, and validation for facilities,utilities, andequipment in the pharmaceutical and biotechindustries. Ourengineers play a critical role ...
Validation Engineer information
See salary details
$22.60 - $27.64
2% of jobs
$27.64 - $32.69
6% of jobs
$32.69 - $37.74
13% of jobs
$39.32 is the 25th percentile. Wages below this are outliers.
$37.74 - $42.79
13% of jobs
$42.79 - $47.84
11% of jobs
The median wage is $50.36 / hr.
$47.84 - $52.88
12% of jobs
$52.88 - $57.93
9% of jobs
$61.82 is the 75th percentile. Wages above this are outliers.
$57.93 - $62.98
13% of jobs
$62.98 - $68.03
13% of jobs
$68.03 - $73.08
6% of jobs
$73.08 - $78.13
3% of jobs
$22
$51
$78
How much do validation engineer jobs pay per hour?
As of Jul 13, 2026, the average hourly pay for validation engineer in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.
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Full-time
Re-posted 29 days ago
Job description
Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
- Validation Engineer
Description:
The role demands deep technical expertise across the full validation lifecycle — including URS development, FAT/SAT execution, and Computer System Validation (CSV) — as well as hands-on experience with systems and controls integration. The candidate will drive end-to-end project implementation: from equipment design and installation through startup, commissioning, and qualification.
Key Responsibilities:
- Develop User Requirement Specifications (URS).
- Lead full validation lifecycle activities: FAT, SAT, CSV, equipment integration, and startup.
- Drive process design for new equipment and ensure product design requirements are met.
- Execute commissioning and qualification activities for new and existing equipment.
- Provide technical oversight to ensure equipment meets safety, regulatory, and operational standards.
- Manage suppliers and external vendors on capital projects, controlling scope, cost, and lead time.
- Collaborate with Procurement and Legal on vendor contracts.
- Create and maintain engineering documentation (URS, assembly instructions, bill of process, etc.).
- Optimize equipment design for manufacturability, cost reduction, maintainability, and efficiency.
- Lead design reviews, risk assessments, and FMEA to ensure reliability and performance.
- Ensure compliance with all safety regulations and quality policies, procedures, and GMP standards.
- Apply statistical analysis and SPC systems to support data-driven decision-making.
- Manage multiple priorities and maintain equipment qualification schedules.
Qualifications:
- Bachelor's degree in Engineering or Science.
- Minimum 4 years of engineering experience in pharmaceutical and/or medical device industries.
- Demonstrated experience across the full validation lifecycle (URS, FAT, SAT, CSV).
- Proven track record supporting full project implementation: design, installation, startup, commissioning, and qualification.
- Strong experience executing capital projects within GMP-regulated manufacturing environments.
- Familiarity with GMP, ISO standards, Lean Manufacturing, and FDA-regulated environments.
- Ability to work independently and lead solutions under general direction.
- Strong organization, and communication skills
At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.