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Supplier Validation Engineer Jobs (NOW HIRING)

Verification & Validation Engineer To support our extraordinary teams who build great products and ... Support supplier validation and component qualification activities when necessary. * Performs other ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

Support supplier validation and component qualification activities when necessary. * Performs other ... Bachelor's degree in Mechanical Engineering or related engineering discipline. * At least 5 years ...

Support supplier validation and component qualification activities when necessary. * Performs other ... Bachelor's degree in Mechanical Engineering or related engineering discipline. * At least 5 years ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices ...

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Supplier Validation Engineer information

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$22

$51

$78

How much do supplier validation engineer jobs pay per hour?

As of Jun 6, 2026, the average hourly pay for supplier 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.

What is the difference between Supplier Validation Engineer vs Quality Engineer?

AspectSupplier Validation EngineerQuality Engineer
CredentialsEngineering degree, certifications like CQE or ASQEngineering or technical degree, certifications like CQE or Six Sigma
Work EnvironmentSupplier sites, manufacturing plants, quality departmentsManufacturing facilities, quality assurance labs, office settings
Industry UsageAutomotive, aerospace, electronics, manufacturingAutomotive, electronics, manufacturing, healthcare

The Supplier Validation Engineer focuses on assessing and qualifying suppliers to ensure component quality and compliance, often working directly with suppliers. In contrast, the Quality Engineer concentrates on maintaining product quality within the manufacturing process, addressing defects, and improving quality systems. Both roles require similar certifications and often overlap in industries like automotive and electronics, but their primary focus and work environments differ.

What cities are hiring for Supplier Validation Engineer jobs? Cities with the most Supplier Validation Engineer job openings:
What states have the most Supplier Validation Engineer jobs? States with the most job openings for Supplier Validation Engineer jobs include:
Infographic showing various Supplier Validation Engineer job openings in the United States as of May 2026, with employment types broken down into 96% Full Time, 1% Part Time, and 3% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Full-time

Posted 22 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.