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Validation Processor Jobs (NOW HIRING)

Supermicro

System Validation Engineer

San Jose, CA · On-site

$100K - $113K/yr

Following/developing the disciplined problem-solving process with AI-based validation process flow, you will be responsible for managing, processing and analyzing data from the fields or lab ...

Techvilla Solutions

USB Validation Engineer

Manor, TX · On-site

Maintain test documentation and contribute to improving validation processes. Required Skills * Hands-on experience in USB validation and testing. * Strong understanding of USB devices, interfaces ...

Techvilla Solutions

USB Validation Engineer

Austin, TX · On-site

Maintain test documentation and contribute to improving validation processes. Required Skills * Hands-on experience in USB validation and testing. * Strong understanding of USB devices, interfaces ...

AMRI

Validation Specialist III

Albuquerque, NM · On-site

This role provides advanced technical expertise and strategic guidance on equipment, process, system, and computer system validations in accordance with cGMP, FDA regulations, and industry standards ...

Techvilla Solutions

Maintain test documentation and contribute to improving validation processes. Required Skills * Hands-on experience in USB validation and testing. * Strong understanding of USB devices, interfaces ...

Techvilla Solutions

USB Validation Engineer

Austin, TX · On-site

Maintain test documentation and contribute to improving validation processes. Required Skills * Hands-on experience in USB validation and testing. * Strong understanding of USB devices, interfaces ...

Fujirebio Europe

WI · On-site

Als Process & Validation Engineer speel je een sleutelrol in het ontwikkelen en valideren van productieprocessen, het optimaliseren van onze manufacturing workflows, het uitvoeren van technische ...

Nihon Kohden

Validation Engineer

Guilford, CT · Hybrid

Knowledge of design verification and validation process and practices, preferred. * Knowledge of engineering design, test, and safety standards (IEC 60601-1 4TH Edition, FDA, ISO), preferred.

Defibtech, LLC

Validation Engineer

Guilford, CT · Hybrid

Knowledge of design verification and validation process and practices, preferred. * Knowledge of engineering design, test, and safety standards (IEC 60601-1 4TH Edition, FDA, ISO), preferred.

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How much do validation processor jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for validation processor in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $23.08 and $51.44 per hour, depending on experience, location, and employer.

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Infographic showing various Validation Processor job openings in the United States as of August 2026, with employment types broken down into 91% Full Time, 4% Part Time, and 5% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $82,237 per year, or $39.5 per hour.

Validation Engineer

Cincinnati, OH

Validation & Engineering Group, Inc
See more jobs at Validation & Engineering Group, Incexternal

Full-time

Re-posted 28 days ago

Key responsibilities

  • Lead full validation lifecycle activities including FAT, SAT, CSV, equipment integration, and startup.

  • Develop User Requirement Specifications (URS) and create engineering documentation.

  • Manage equipment commissioning, qualification, and ensure compliance with safety, regulatory, and GMP standards.

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.