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Full Time Computer System Validation Jobs Near Me

PSC Biotech

Validation Engineer

Columbus, OH

$100K - $160K/yr

Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related discipline. * Minimum of 3 years of experience in computerized system validation, automation software, and ...

PSC Biotech

Validation Engineer

Columbus, OH · On-site

Bachelor's degree in Engineering, Computer Science, Life Sciences, or a related discipline. * Minimum of 3 years of experience in computerized system validation, automation software, and ...

PSC Biotech

Validation Engineer

Columbus, OH

... Computer Science, Life Sciences, or a related discipline. Minimum of 3 years of experience in computerized system validation, automation software, and manufacturing systems within regulated life ...

voyant

Engineer, Validation

New Albany, OH · On-site

Develop standards and templates for custom and regulated products. · Advise on engineering and equipment requirements for validation, especially electronic/computer- controlled systems. Assist in ...

Voyant Beauty

Engineer, Validation

New Albany, OH · On-site

Develop standards and templates for custom and regulated products. • Advise on engineering and equipment requirements for validation, especially electronic/computer- controlled systems. Assist in ...

ATS Automation

Automation Engineer

Lewis Center, OH

Partner with Quality Assurance, Computer System Validation (CSV), Packaging, Manufacturing, and IT/OT teams to maintain GxP compliance. * Ensure commissioning and qualification activities align with ...

Forge Biologics

CSV Engineer I

Columbus, OH

Supports computer system validation efforts for Veeva Vault QMS, BMRAM (laboratory information ... Annual bonus opportunities for all full-time team members. * 401(k) with company match to help you ...

Forge Biologics

CSV Engineer I

Columbus, OH

Supports computer system validation efforts for Veeva Vault QMS, BMRAM (laboratory information ... Annual bonus opportunities for all full-time team members. * 401(k) with company match to help you ...

Forge Biologics

CSV Engineer I

Columbus, OH · On-site

Supports computer system validation efforts for Veeva Vault QMS, BMRAM (laboratory information ... Annual bonus opportunities for all full-time team members. * 401(k) with company match to help you ...

Inteldot

Automation Engineer

New Albany, OH · On-site

Partner with Quality Assurance, Computer System Validation (CSV), Packaging, Manufacturing, and IT/OT teams to maintain GxP compliance. * Ensure commissioning and qualification activities align with ...

Inteldot

Automation Engineer

New Albany, OH · On-site

Partner with Quality Assurance, Computer System Validation (CSV), Packaging, Manufacturing, and IT/OT teams to maintain GxP compliance. * Ensure commissioning and qualification activities align with ...

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Full Time Computer System Validation information

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How much do full time computer system validation jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for full time computer system validation in the United States is $54.32, according to ZipRecruiter salary data. Most workers in this role earn between $41.83 and $64.42 per hour, depending on experience, location, and employer.
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Full Time Computer System Validation jobs near you
A map of the United States highlighting the number of Full Time Computer System Validation job openings by state according to ZipRecruiter. The image is accompanied by a detailed chart listing the number of Full Time Computer System Validation job openings in each state, with California having the most at 2 and Hawaii the least at 0.

Validation Engineer

Validation & Engineering Group, Inc

New Albany, OH

Full-time

Re-posted 2 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.