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Validation Engineer Jobs in Colorado (NOW HIRING)

Validation Project Lead Location : Boulder, CO Compli, LLC was founded in 2001 to provide ... Bachelor's degree in related life sciences or engineering field * 7-10 years of GMP experience

Validation Project Lead

Boulder, CO · On-site

$95K - $130K/yr

Validation Project Lead Location : Boulder, CO Compli, LLC was founded in 2001 to provide ... Bachelors degree in related life sciences or engineering field * 7-10 years of GMP experience

Validation Project Lead Location : Boulder, CO Compli, LLC was founded in 2001 to provide ... Bachelor's degree in related life sciences or engineering field * 7-10 years of GMP experience

Test Engineer LOCATION Aurora, CO 80014 CLEARANCE TS/SCI Full Poly (Please note this position ... validate the functionality, performance, and security of our applications. You will work closely ...

This role is responsible for executing verification, validation, and automated testing across end ... The engineer will ensure that ground system platforms securely and seamlessly integrate with our ...

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Validation Engineer information

See Colorado salary details

$23

$54

$82

How much do validation engineer jobs pay per hour?

As of Jul 20, 2026, the average hourly pay for validation engineer in Colorado is $54.67, according to ZipRecruiter salary data. Most workers in this role earn between $41.44 and $66.49 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.
What are the most commonly searched types of Validation Engineer jobs in Colorado? The most popular types of Validation Engineer jobs in Colorado are:
What are popular job titles related to Validation Engineer jobs in Colorado? For Validation Engineer jobs in Colorado, the most frequently searched job titles are:
What cities in Colorado are hiring for Validation Engineer jobs? Cities in Colorado with the most Validation Engineer job openings:
Infographic showing various Validation Engineer job openings in Colorado as of July 2026, with employment types broken down into 91% Full Time, 6% Part Time, and 3% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $113,724 per year, or $54.7 per hour.
Validation Project Lead

Validation Project Lead

Compli

Boulder, CO

$95K - $130K/yr

Full-time

Posted 13 days ago


Job description

Job: Validation Project Lead

Location: Boulder, CO


Compli, LLC was founded in 2001 to provide commissioning, validation, and regulatory support services to the life sciences industry. We serve pharmaceutical companies across the U.S. Regarding regulations and compliance, it has never been more important to understand the documentation and quality assurance activities as they relate to vendors, engineering, construction, and contractors, which is why clients trust the Compli team.

Compli LLC is a full-service regulatory compliance consulting services company with a life sciences division specializing in pharma, biotech, API, Medical devices, and laboratory facilities. We are seeking an experienced Validation professional to join our growing team


What You'll Do:
  • Function as an owner’s representative and report to the client’s management lead
  • Coordinate internal and external resources for the flawless execution of projects
  • Able to lead and execute projects to meet client’s priorities
  • Ensure that projects are delivered on time and within scope.
  • Assist in the definition of project scope and objectives, involving all relevant stakeholders and ensuring technical feasibility
  • Develop a detailed project plan to monitor and track progress
  • Manage changes to the project scope, project schedule and project costs using appropriate verification techniques
  • Measure project performance using appropriate tools and techniques
  • Support Client commissioning/validation for facility, utility, equipment, cleaning, and process validation projects
  • Prepare and execute commissioning/validation lifecycle documents
  • Participate in any stage of clinical or commercial production including green field construction, facility renovation, new product development, product launch, or product/process upgrade
  • Write summary reports for validation and qualification protocols
  • Support project milestones, priorities, and deadlines
  • Write operating procedures for technical equipment and practices and procedures
  • Perform system and process risk assessments and analyses
  • Schedule and coordinate protocol execution with other departments including manufacturing, facilities, and project management
  • Develop project-specific validation plans and strategy
  • Other duties as assigned.

What You'll Bring:
  • Bachelor’s degree in related life sciences or engineering field
  • 7-10 years of GMP experience
  • Ability to converse about scientific matters
  • Ability to work independently or in collaboration with others
  • In-depth understanding and application of validation principles, concepts, practices, and standards
  • Proficient in current Good Manufacturing Practices and other applicable regulations
  • Experienced with all pertinent industry best practices (e.g., ISPE) including development and execution of all applicable system life cycle deliverables (e.g., URS, SRS, FRS, DDS, RTM, Unit, Integration, User Acceptance testing, FAT, SAT, Validation Planning, IQ, OQ, PQ, Final Validation Summary Report
  • Demonstrated expertise in at least one aspect of system qualification and regulatory compliance (e.g., EMEA, GCP, GLP, GMP, QSR) and internal requirements employing regulatory guidance and industry standards
  • Excellent written communication skills with emphasis on technical writing
  • Proficient in MS Excel, MS Word, MS Project, MS PowerPoint, and AutoCAD Lite.

Travel: Prefer local to the Denver Metropolitan Area

Compensation: $95,000-$130,000 yearly

*This role is not open to C2C staffing.


Perks of the Job:

· Competitive Pay commensurate with experience

· Work / Life Balance

· Working with a small, close-knit team where you are valued as an individual

· A learning environment and continuous advancement opportunities


Join Our Team

Apply today and build your future with GBA.

At Compli, we are about innovative and intelligent people who want to solve problems. We’re known for our technical excellence, but we bring so much more to the table. We strive to create remarkable solutions for a higher quality of life. And we are changing the industry by integrating the design and construction process with use of new technology.

GBA is an Equal Employment Opportunity Employer. We promote diversity in our workforce by including all individuals regardless of age, race, religion, color, sex, national origin, marital status, genetic information, sexual orientation, gender identity, gender expression, disability, veteran status, pregnancy status, or any other status protected by law.