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System Validation Engineer At Intel Jobs (NOW HIRING)

Intel Corporation

GPU Validation Engineer

Folsom, CA · On-site

Life at Intel: As a GPU Design Verification Engineer, you will play a critical role in defining and ... Define and execute verification plans, running system simulation models to identify bugs, analyze ...

Intel

CPU Validation Engineer

Austin, TX · On-site

$91K - $149K/yr

Intel is a company of bold and curious inventors and problem solvers who create some of the most ... RTL Debugging at module level or soc level system simulation failures. * Knowledge of basic lab ...

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How much do system validation engineer at intel jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for system validation engineer at intel in the United States is $51.80, according to ZipRecruiter salary data. Most workers in this role earn between $38.94 and $64.42 per hour, depending on experience, location, and employer.

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

To thrive as a System Validation Engineer at Intel, you need a strong background in computer engineering or electrical engineering, along with experience in hardware and software validation methodologies. Familiarity with validation tools like oscilloscopes, logic analyzers, scripting languages (such as Python or Perl), and exposure to system-level test automation frameworks is typically required, along with relevant certifications being a plus. Strong analytical thinking, problem-solving skills, and effective communication are crucial soft skills for diagnosing issues and collaborating with cross-functional teams. These competencies are essential for ensuring product quality, identifying system defects early, and driving successful product launches in a fast-paced technology environment.

What are some common challenges System Validation Engineers at Intel face during the validation process, and how can they overcome them?

System Validation Engineers at Intel often encounter challenges such as rapidly evolving hardware specifications, tight project deadlines, and the need to coordinate across multiple cross-functional teams. Navigating these demands requires strong problem-solving skills, proactive communication, and adaptability. Engineers can overcome these hurdles by maintaining thorough documentation, staying updated on the latest validation tools and methodologies, and actively collaborating with design, firmware, and software teams to address issues early in the development cycle.

What does a System Validation Engineer do at Intel?

A System Validation Engineer at Intel is responsible for ensuring that computer hardware and software systems function correctly and meet all design specifications before they are released to customers. They develop and execute test plans, debug issues, and work closely with design and development teams to identify and resolve any system-level problems. Their work involves both hardware and software validation, often using automated tools and scripts to simulate real-world usage and stress scenarios. This role is vital in maintaining Intel's standards for performance, reliability, and quality in its products.
Infographic showing various System Validation Engineer At Intel job openings in the United States as of May 2026, with employment types broken down into 20% Locum Tenens, 10% As Needed, and 70% Full Time. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution, with an average salary of $107,747 per year, or $51.8 per hour.
Computer System Validation Engineer

Computer System Validation Engineer

Katalyst HealthCares & Life Sciences

Princeton, NJ • On-site

Full-time

Posted 11 days ago

Job description

Csv Specialist

The CSV Specialist is responsible for planning, coordinating, and executing validation activities for computer systems to ensure compliance with regulatory requirements. This role involves working closely with IT, Quality Assurance, and business stakeholders to validate new and existing systems, document validation evidence, and support audits and inspections.

Roles & responsibility:

  • Knowledge on FDA Guidance's and industry Standards
  • Develop and execute validation plans, protocols (IQ/OQ/PQ), and reports for computer systems.
  • Assess and document system requirements, risk assessments, and user requirements specifications (URS).
  • Review and approve system design, configuration, and test documentation.
  • Ensure compliance with regulatory requirements (e.g., FDA 21 CFR Part 11, GAMP 5, EU Annex 11).
  • Manage change control and deviation management processes for validated systems.
  • Collaborate with cross-functional teams (IT, QA, business users) to ensure validation deliverables are met.
  • Maintain validation documentation and support periodic reviews and revalidation.
  • Participate in internal and external audits and respond to regulatory inquiries.
  • Train users and stakeholders on validated systems and compliance requirements.
  • Stay current with industry trends, regulations, and best practices in computer system validation.

Education & Experience:

  • Bachelor's degree in Computer Science, Life Sciences, Engineering, or related field.
  • 2+ years of experience in computer system validation or a regulated industry.
  • Knowledge of applicable regulations (FDA, EMA, GxP, 21 CFR Part 11, Annex 11).
  • Experience with validation methodologies (GAMP 5, risk-based validation).
  • Strong documentation, analytical, and problem-solving skills.
  • Excellent communication and teamwork abilities.
  • Experience with ERP, LIMS, MES, or other regulated systems is a plus
  • Familiarity with project management tools and methodologies
  • Experience with audit preparation and participation.
  • Understanding of data integrity principles.
  • Certification in validation or quality assurance (e.g., ASQ, ISPE) is a plus.
  • Prior work experience in Medical Device Industry, Biotechnology or Pharmaceutical industry is a plus.
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About Katalyst Healthcares & Life Sciences

Sourced by ZipRecruiter

Katalyst HealthCares & Life Sciences is a Global Contract Research Organization that provides services in Clinical Research, Manufacturing & Quaity, Regulatory Affairs Areas.. Industries Serving: Pharmaceutical Bio-Pharmaceutical Medical Device Cosmeceuticals & Cosmetics Food & Beverage Clinical Research Scientific Areas Covering: Clinical Research Manufacturing Quality & Validations Regulatory Affairs Intellectual Property Through our in-house team expertise, associates and alliances in the US, Europe and Asia, we can rapidly deliver services, technology, processes and workforce globally, either virtually or integrate into client project space, providing oversight and expertise for individual needs to total end-to-end support for all kinds of clinical trials of Pharma, Biotech, Medical Device and all other scientific products and their manufacturing.

Industry

Scientific research and development services

Company size

51 - 200 Employees

Headquarters location

South Plainfield, NJ, US

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