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Window Device Driver Validation Engineer Jobs (NOW HIRING)

... device, or other regulated life sciences facilities. * Develop, review, and execute validation ... Review engineering and technical documentation to ensure validation requirements are adequately ...

... device, or other regulated life sciences facilities. * Develop, review, and execute validation ... Review engineering and technical documentation to ensure validation requirements are adequately ...

... device, or other regulated life sciences facilities. * Develop, review, and execute validation ... Review engineering and technical documentation to ensure validation requirements are adequately ...

... device, or other regulated life sciences facilities. * Develop, review, and execute validation ... Review engineering and technical documentation to ensure validation requirements are adequately ...

... device, or other regulated life sciences facilities. * Develop, review, and execute validation ... Review engineering and technical documentation to ensure validation requirements are adequately ...

... device, or other regulated life sciences facilities. * Develop, review, and execute validation ... Review engineering and technical documentation to ensure validation requirements are adequately ...

A validation engineer develops a comprehensive test plan by utilizing design specifications ... device drivers and test bench scripts. • Developing block, subsystem and system level test FW and ...

Caguas, Puerto Rico | Posted on 07/30/2026 We are seeking a Validation Engineer to support equipment validation activities in a medical device manufacturing environment (21 CFR Part 820 / ISO 13485)

A validation engineer develops a comprehensive test plan by utilizing design specifications ... device drivers and test bench scripts. • Developing block, subsystem and system level test FW and ...

Caguas, Puerto Rico | Posted on 07/30/2026 We are seeking a Validation Engineer to support equipment validation activities in a medical device manufacturing environment (21 CFR Part 820 / ISO 13485)

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 ...

Characterize device performance and identify deviations from specification * Identify, document ... Collaborate with IC design engineers to validate functional correctness and resolve performance ...

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 ...

Showing results 41-60

Window Device Driver Validation Engineer information

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$22

$51

$78

How much do window device driver validation engineer jobs pay per hour?

As of Sep 15, 2026, the average hourly pay for window device driver 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 does a window device driver validation engineer do?

A Windows Device Driver Validation Engineer is responsible for testing and validating hardware device drivers to ensure they work correctly with the Windows operating system. They develop automated and manual test cases, identify compatibility issues, and work closely with developers to resolve bugs. Their work ensures that hardware components like printers, network cards, and graphics adapters function seamlessly on Windows platforms, contributing to system stability and user experience.

What are the key skills and qualifications needed to thrive as a window device driver validation engineer?

To thrive as a Window Device Driver Validation Engineer, you need a solid background in computer engineering or related fields, strong knowledge of Windows OS internals, and experience with driver development and validation processes. Familiarity with tools such as Windows Driver Kit (WDK), debuggers like WinDbg, and automated test frameworks is often required, along with relevant certifications in software testing or Microsoft technologies. Analytical thinking, detail orientation, and effective communication are crucial soft skills for diagnosing complex issues and collaborating with cross-functional teams. These skills ensure reliable driver performance, system stability, and successful product releases in a highly technical environment.

What are some common challenges faced by a window device driver validation engineer, and how can they be addressed?

Windows Device Driver Validation Engineers often encounter challenges such as debugging complex driver failures, ensuring compatibility across multiple Windows versions, and staying current with evolving hardware and software standards. To address these, engineers typically collaborate closely with development teams, utilize automated testing tools, and participate in continuous learning through technical forums and training. Proactive communication and thorough documentation are also key to efficiently resolving issues and maintaining high-quality driver performance.

What is the difference between Window Device Driver Validation Engineer vs Windows Driver Developer?

AspectWindow Device Driver Validation EngineerWindows Driver Developer
Primary FocusTesting and validating device drivers for compatibility and stabilityDesigning, developing, and coding device drivers
Skills RequiredTesting methodologies, debugging, knowledge of Windows OS, driver validation toolsProgramming languages (C/C++), driver architecture, Windows Driver Model (WDM)
Work EnvironmentTesting labs, validation teams, quality assuranceDevelopment teams, software engineering environments
CertificationsOften requires certifications in testing or Windows OSRequires programming and driver development certifications or experience

The main difference is that Window Device Driver Validation Engineers focus on testing and validating drivers to ensure they work correctly within Windows environments, while Windows Driver Developers are responsible for creating and coding the drivers themselves. Both roles require knowledge of Windows OS and driver architecture, but their core responsibilities differ significantly.

What are popular job titles related to Window Device Driver Validation Engineer jobs?

For Window Device Driver Validation Engineer jobs, the most frequently searched job titles are:

Infographic showing various Window Device Driver Validation Engineer job openings in the United States as of September 2026, with employment types broken down into 1% As Needed, 74% Full Time, 23% Part Time, and 2% Contract. Highlights an 98% Physical, and 2% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer

Wilson, NC • On-site

Pinnaql
Pharmaceutical and Medicine Manufacturing • 11 - 50 employees

Full-time

Re-posted 2 days ago


Job description

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 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

Position Overview
We are seeking an experienced Validation Engineer with Commissioning, Qualification & Validation (CQV) experience to support projects within the life sciences industry. The successful candidate will be responsible for executing and documenting commissioning, qualification, and validation activities for facilities, utilities, equipment, systems, and manufacturing processes in accordance with applicable regulatory requirements and Good Manufacturing Practices (GMP).
This role requires strong technical documentation skills, attention to detail, and the ability to work collaboratively with Engineering, Quality, Manufacturing, Automation, and Project Management teams.
Key Responsibilities
  • Execute and support Commissioning, Qualification & Validation (CQV) activities for pharmaceutical, biotechnology, medical device, or other regulated life sciences facilities.
  • Develop, review, and execute validation documentation, including:
    • Validation Plans
    • User Requirements Specifications (URS)
    • Risk Assessments
    • Design/Functional Specifications
    • Commissioning documentation
    • IQ/OQ/PQ protocols and reports
    • Traceability Matrices
    • Summary Reports
  • Support qualification of equipment, facilities, utilities, and manufacturing systems.
  • Perform protocol execution, field verification, data collection, and review of qualification results.
  • Ensure validation activities are performed in compliance with GMP, FDA, EU GMP, and applicable industry standards.
  • Participate in FMEA/risk assessments and apply a risk-based approach to validation activities.
  • Support deviations, investigations, CAPA, and change control activities associated with validation projects.
  • Review engineering and technical documentation to ensure validation requirements are adequately addressed.
  • Collaborate with Engineering, Quality Assurance, Manufacturing, Automation, Facilities, and other project stakeholders.
  • Track validation deliverables, schedules, open items, and project milestones.
  • Support commissioning activities and transition from commissioning into formal qualification.
  • Ensure validation documentation is complete, accurate, and audit-ready.
  • Participate in client meetings, project status meetings, and technical reviews.
  • Provide technical support during regulatory or client inspections, as required.

CQV Experience
Candidates should have hands-on experience with some combination of:
  • Commissioning and qualification of process equipment
  • Facility and utility qualification
  • Cleanrooms and controlled environments
  • HVAC systems
  • Purified Water / WFI systems
  • Compressed gases and process gases
  • Autoclaves, sterilizers, and/or depyrogenation equipment
  • Manufacturing and laboratory equipment
  • Temperature-controlled systems
  • Process systems and supporting utilities
  • Equipment and system turnover documentation
  • IQ/OQ/PQ execution

Required Qualifications
  • Bachelor's degree in Engineering, Science, or a related technical discipline.
  • 3+ years of validation, qualification, commissioning, or CQV experience within a regulated life sciences environment.
  • Experience working in pharmaceutical, biotechnology, medical device, or other GMP-regulated industries.
  • Strong understanding of GMP and validation principles.
  • Experience developing and/or executing validation and qualification protocols.
  • Experience with risk-based validation methodologies.
  • Strong technical writing and documentation skills.
  • Ability to interpret engineering drawings, specifications, procedures, and technical documentation.
  • Strong organizational and project management skills.
  • Ability to work independently and collaboratively in a project environment.

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.