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Equipment Validation Engineer Jobs (NOW HIRING)

Validation & Engineering Group, Inc

PR · On-site

Experience supporting various manufacturing equipment and/or systems, as well as Cleaning Validation. * Among other related activities. At Validation & Engineering Group, people always come first. We ...

INCOG

Senior Validation Engineer

Fishers, IN · On-site

The Senior Validation Engineer is responsible for understanding and implementing validation ... Perform Qualification activities on utilities, equipment and laboratory systems. This includes, but ...

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Equipment Validation Engineer information

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How much do equipment validation engineer jobs pay per hour?

As of Jul 23, 2026, the average hourly pay for equipment validation engineer in the United States is $63.77, according to ZipRecruiter salary data. Most workers in this role earn between $52.64 and $69.71 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an Equipment Validation Engineer, and why are they important?

To thrive as an Equipment Validation Engineer, you need a strong background in engineering principles, process validation, and regulatory standards such as GMP, typically supported by a degree in engineering or a related field. Familiarity with validation protocols (IQ/OQ/PQ), data analysis software, and documentation systems is essential, and certifications like Six Sigma or CQE can be advantageous. Attention to detail, strong problem-solving skills, and effective communication are critical soft skills for this role. These competencies ensure equipment operates reliably and compliantly, supporting product quality and regulatory approval in highly regulated industries.

What is the difference between Equipment Validation Engineer vs Quality Assurance Engineer?

AspectEquipment Validation EngineerQuality Assurance Engineer
CertificationsGMP, GxP, Validation certificationsISO, Six Sigma, QA certifications
Work EnvironmentManufacturing, pharmaceutical, biotech facilitiesManufacturing, software, service industries
Primary FocusValidating equipment and systems for complianceEnsuring product quality and process adherence

The Equipment Validation Engineer primarily focuses on validating equipment and systems to meet regulatory standards, ensuring operational compliance. In contrast, the Quality Assurance Engineer concentrates on maintaining overall product quality and process improvements. Both roles are essential in regulated industries but serve different aspects of quality management.

How does an Equipment Validation Engineer typically collaborate with cross-functional teams during a validation project?

As an Equipment Validation Engineer, you will regularly work alongside quality assurance, manufacturing, engineering, and regulatory teams. Your role involves gathering input from these departments to develop comprehensive validation protocols and ensure equipment meets necessary standards. Effective communication and project management skills are essential, as you'll coordinate timelines, document results, and ensure that all stakeholders are aligned throughout the validation process. This collaborative environment offers valuable exposure to various functions within the organization and fosters both technical and interpersonal skill development.

What are Equipment Validation Engineers?

Equipment Validation Engineers are professionals responsible for ensuring that manufacturing equipment and systems operate according to required specifications and regulatory standards. They develop and execute validation protocols, conduct equipment testing, and document results to demonstrate compliance with industry guidelines, such as those set by the FDA or ISO. Their work is essential in industries like pharmaceuticals, biotechnology, and medical devices, where validated equipment is critical to product safety and quality.
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Equipment Validation Engineer jobs near you
Infographic showing various Equipment Validation Engineer job openings in the United States as of July 2026, with employment types broken down into 96% Full Time, 1% Part Time, and 3% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $132,650 per year, or $63.8 per hour.

Validation Engineer

Validation & Engineering Group Inc.

Greenville, NC • On-site

Other

Posted 8 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.

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