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Validation Engineer Jobs in Utah (NOW HIRING)

Petersen Inc

Design Engineer

Ogden, UT · On-site

Summary Of Position The Design Engineer develops and validates custom equipment, structures, and mechanical systems with an emphasis on mechanical design, engineering analysis, and real-world ...

HX5 LLC

Electrical Engineer

Ogden, UT · On-site

Electrical Engineer Electrical Engineer Jrym Hill Air Force Base Ogden UT HX5 is an award-winning ... Develop and/or refine system features, enhancing, extending, or validating existing processes, data ...

Sterling Engineering

UT

$75/hr

... and design validation testing activities Develop and maintain test fixtures and testing ... Bachelor's degree in Engineering required; Master's degree preferred Experience in test and ...

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How much do validation engineer jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for validation engineer in Utah is $47.34, according to ZipRecruiter salary data. Most workers in this role earn between $35.87 and $57.55 per hour, depending on experience, location, and employer.

What Is a Validation Engineer?

A validation engineer is responsible for testing equipment and electrical systems used in the manufacturing process. As a validation engineer, your primary duty is to work with the other members of the validation team to ensure that these systems measure up to company and industry standards. Skills needed for a validation engineer job include the ability to accurately test, measure, and calibrate manufacturing equipment for maximum efficiency and quality.

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

AspectValidation EngineerQuality Assurance Engineer
CertificationsGMP, ISO, Six SigmaISO, Six Sigma, CQA
Work EnvironmentRegulated industries like pharma, biotech, medical devicesManufacturing, software, and product development
Primary FocusEnsuring products meet specifications through validation processesPreventing defects through process and system improvements
Common UsageRegulatory compliance, validation protocolsProcess audits, quality systems

Validation Engineers focus on verifying that products and processes meet regulatory standards through validation protocols, especially in regulated industries. Quality Assurance Engineers concentrate on maintaining overall product quality by implementing and auditing quality systems. While both roles aim to ensure product safety and efficacy, Validation Engineers are more involved in validation activities, whereas QA Engineers focus on process improvement and defect prevention.

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

To thrive as a Validation Engineer, you need a solid background in engineering, quality assurance, and regulatory compliance, typically backed by a degree in engineering or a related field. Familiarity with validation protocols, statistical analysis tools, and industry-specific regulations such as FDA, GMP, or ISO standards is essential. Strong analytical thinking, attention to detail, and effective communication set top performers apart in this role. These skills ensure that products and processes meet stringent quality and safety standards, minimizing risks and ensuring regulatory approval.

What are some common challenges Validation Engineers face when working cross-functionally with other departments?

Validation Engineers frequently collaborate with teams such as manufacturing, quality assurance, and research & development. One common challenge is aligning differing priorities and timelines between departments, which can sometimes delay validation projects. Effective communication skills and flexibility are crucial to navigating these cross-functional interactions, ensuring that all regulatory and quality requirements are met without hindering production schedules. Building strong working relationships and proactively addressing potential concerns can help Validation Engineers facilitate smoother project execution.

What are Validation Engineers?

Validation Engineers are professionals responsible for ensuring that systems, processes, or equipment meet regulatory standards and function as intended. They typically work in industries such as pharmaceuticals, biotechnology, manufacturing, and medical devices. Their duties involve creating validation protocols, conducting tests, analyzing data, and documenting results to ensure compliance with industry regulations and quality standards. Validation Engineers play a critical role in maintaining product safety and efficacy, as well as helping companies pass audits and inspections.
More about Validation Engineer jobs
What are the most commonly searched types of Validation Engineer jobs in Utah? The most popular types of Validation Engineer jobs in Utah are:
What are popular job titles related to Validation Engineer jobs in Utah? For Validation Engineer jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Validation Engineer jobs in Utah look for? The top searched job categories for Validation Engineer jobs in Utah are:
What are popular job titles related to Validation Engineer jobs in UT? For Validation Engineer jobs in UT, the most frequently searched job titles are:
Validation Engineer jobs near you
Infographic showing various Validation Engineer job openings in Utah as of June 2026, with employment types broken down into 92% Full Time, 5% Part Time, and 3% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $98,459 per year, or $47.3 per hour.
Quality Engineer II, Validation & Sustaining

Quality Engineer II, Validation & Sustaining

ICU Medical

Salt Lake City, UT • On-site

$69K - $90K/yr

Full-time

Posted 7 days ago

ICU Medical rating

7.8

Company rating: 7.8 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

163rd of 518 rated manufacturers

Job description

Job Description
Position Summary
This role is critical to ensuring that all processes, equipment, and systems involved in the manufacturing and development of ICU Products meet the highest standards of quality and regulatory compliance. The Quality Engineer II, Sustaining will work closely with cross-functional teams, including R&D, Advanced Manufacturing Engineering, Manufacturing, and Quality Assurance, to validate equipment, processes, and software used in production.
Essential Duties & Responsibilities
  • Demonstrate an understanding and functional impact of changes to critical process in the manufacturing and testing of ICU products.
  • Develop and execute validation protocols (IQ/OQ/PQ) for manufacturing equipment, processes, and software systems.
  • Conduct risk assessments to identify critical quality attributes (CQAs) and critical process parameters (CPPs) for validation.
  • Create and review Quality Control Plans and process FMEA's,
  • Ensure validation documentation is accurate, complete, and in accordance with regulatory and quality system requirements.
  • Maintain validation master plans, protocols, and reports as part of the company's quality system documentation.
  • Improve the Quality Management System through internal audits and supporting regulatory audits.
  • Lead and support the validation of new and existing manufacturing processes, ensuring compliance with FDA regulations, ISO 13485 standard, and company quality systems.
  • Develop and execute Test Method Validations for manufacturing processes and laboratory equipment, as needed
  • Must be able to apply a well-rounded understanding of engineering/design specifications, and engineering principles and methods, to perform analysis and resolve problems of moderate complexity.
  • Write effective reports and do so in a timely, priority driven manner, working effectively in a team environment with shifting priorities and time sensitive requirements.
  • Updates Standard Operating Procedures and related QMS documentation, to complete improvement projects, as required.
  • Establish and maintain communication both internal and external (with the customers, molding, automation, assembly, product engineering, project management and regulatory personnel as needed)
  • Continually improve knowledge of relevant quality/regulatory topics and changes.

Knowledge, Skills & Qualifications
  • Knowledge of Agile PLM / Oracle (Desirable)
  • Knowledge of basic Geometric Dimensioning & Tolerancing (GD&T) concepts.
  • Proficient in Minitab and Microsoft Office Suite
  • Strong communication skills and the ability to work collaboratively with cross-functional teams.
  • Able to multitask and work in a fast-paced environment.
  • High level of attention to detail and strong organizational skills.

Education and Experience
  • Must be at least 18 years of age
  • Bachelor's degree in STEM from an accredited college or university
  • 2-4 years' experience working in a regulated manufacturing or pharmaceutical/healthcare environment required. Prior experience in quality is preferred.
  • Proficiency in using validation software and other relevant tools (e.g., Minitab, statistical analysis software).
  • Strong knowledge of medical device validation processes, risk management, and regulatory requirements (FDA 21 CFR Part 820, ISO 14971, ISO 13485).

Physical Requirements and Work Environment
  • This is largely a sedentary role.
  • This job operates in a professional office environment and routinely uses standard office equipment.
  • Work is partly performed in a clean room environment
  • Must be able to occasionally move and lift objects of up to 25 lbs
  • Typically requires travel less than 5% of the time

About Us
ICU Medical has consistently provided you with clinical innovations that help solve real-world challenges.
With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically-essential IV therapy and high-value critical care products for hospital, alternate site, and home care settings.
We're ready to bring you consistent quality, innovation, and value in more areas than ever. Our focus allows us to bring you:
  • Dedicated and non-dedicated IV sets and needlefree connectors clinically proven to provide an effective barrier against bacterial transfer and colonization.
  • The industry's broadest IV smart pump offering covering large volume, pain management, and ambulatory needs.
  • IV medication safety software providing full IV-EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company.
  • Significant US IV solutions manufacturing and supply capabilities.

ICU Medical EEO Statement:
ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status.
If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at humanresources@icumed.com. We are committed to providing equal access and opportunities for all candidates.
ICU Medical EEO Policy Statement
Know Your Rights: Workplace Discrimination is Illegal Poster
ICU Medical CCPA Notice to Job Applicants

What ICU Medical employees say

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Benefits

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Workplace

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About ICU Medical

Sourced by ZipRecruiter

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

San Clemente, CA, US

Year founded

1984

Social media

Twitter

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