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Embedded System Validation Engineer Jobs in Fairfield, NJ

CACI

Embedded Software Engineer

Florham Park, NJ

$94K - $198K/yr

In this role, you'll work across realtime embedded systems, network technologies, and missioncritical cybersecurity solutions. You'll collaborate with engineers, analysts, and customers to solve ...

Checkpoint Systems

Be Seen First

System Test Engineer

Thorofare, NJ · On-site

$85K - $102K/yr

The System Test Engineer validates embedded Linux-based devices, including RFID readers and edge computing platforms, by executing and evolving test strategies that cover hardware, firmware, embedded ...

ZT Systems

Mechanical Validation Engineer

Secaucus, NJ · On-site

The Mechanical Validation Engineer will be working with cross functional teams to aid in developing ... Understand how systems work and be able to identify defects and issues * Confidently describe test ...

ZT Systems

Electrical Validation Engineer

Secaucus, NJ · On-site

The Electrical Validation Engineer will be working with cross functional teams to aid in developing ... Understand how systems work and be able to identify defects and issues * Confidently describe test ...

Fusion Energy Base

Embedded Systems Engineer

Kearny, NJ · On-site

$80 - $110/hr

Position Overview Thea Energy is seeking a skilled and motivated Embedded Systems Engineer to lead ... You will interface with internal system owners, power electronics vendors, and control software ...

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All JobsEmbedded System Validation Engineer JobsEmbedded System Validation Engineer Jobs in Fairfield, NJ

Embedded System Validation Engineer information

See Fairfield, NJ salary details

$63.7K

$140K

$195.8K

How much do embedded system validation engineer jobs pay per year?

As of Sep 5, 2026, the average yearly pay for embedded system validation engineer in Fairfield, NJ is $139,957.00, according to ZipRecruiter salary data. Most workers in this role earn between $113,700.00 and $166,700.00 per year, depending on experience, location, and employer.

What is an embedded system validation engineer?

Embedded System Validation Engineers are professionals responsible for testing and verifying that embedded systems—specialized computing systems within larger devices—function correctly and meet design specifications. They develop and execute validation plans, create test cases, and use debugging tools to identify hardware and software issues. Their work ensures the reliability, safety, and performance of products such as automotive systems, medical devices, and consumer electronics. Collaboration with design and development teams is crucial to address any detected issues before product release.

What are some common challenges faced by embedded system validation engineers during product testing?

Embedded System Validation Engineers often encounter challenges such as debugging complex hardware-software interactions, managing limited access to prototypes, and ensuring thorough test coverage across various hardware configurations. Collaborating closely with firmware developers and hardware designers is essential to identify and resolve issues efficiently. Additionally, staying updated with new validation tools and methodologies can be necessary to address evolving technology and product requirements.

What are the key skills and qualifications needed to thrive as an embedded system validation engineer, and why are they important?

To excel as an Embedded System Validation Engineer, a strong background in embedded systems, electronics, and programming languages like C/C++ is essential, typically supported by a degree in electrical engineering or a related field. Familiarity with validation tools, oscilloscopes, logic analyzers, version control systems, and test automation frameworks is commonly required. Analytical thinking, problem-solving, and effective communication are vital soft skills for diagnosing complex issues and collaborating with cross-functional teams. These abilities ensure comprehensive system validation, high product quality, and successful integration in complex hardware-software environments.

What is the difference between Embedded System Validation Engineer vs Firmware Test Engineer?

AspectEmbedded System Validation EngineerFirmware Test Engineer
CredentialsBachelor's in Electrical, Computer Engineering, or related; certifications like ISTQB are commonBachelor's in Computer Science, Electrical Engineering; similar certifications often used
Work EnvironmentHardware and software testing in embedded systems, often in labs or manufacturingSoftware testing of firmware, mainly in development or testing labs
Industry UsageAutomotive, consumer electronics, industrial automationConsumer electronics, IoT devices, embedded systems
Common Search/ComparisonYesYes

The Embedded System Validation Engineer focuses on validating both hardware and software components of embedded systems, ensuring overall system functionality. In contrast, the Firmware Test Engineer primarily tests the firmware or software running on embedded devices. While both roles require similar technical skills and certifications, their focus areas differ: validation of entire systems versus software-specific testing.

What cities near Fairfield, NJ are hiring for Embedded System Validation Engineer jobs?

Cities near Fairfield, NJ with the most Embedded System Validation Engineer job openings:

Embedded System Validation Engineer jobs near you

Validation - Engineer (m/f/d) (Remote)

Frontwell Solutions

Dover, DE • On-site

$110 - $150/hr

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Job description

Join FrontWell Solutions, a leader in Laboratory Information Management Systems, Manufacturing IT, and Quality Assurance solutions for the life sciences sector. As a trusted consulting partner, we deliver advanced, compliant, and innovative digital solutions that drive operational excellence and regulatory success for our clients. Our expertise spans the full spectrum of pharmaceutical and biotech IT, with a focus on quality, compliance, and digital transformation.
Position Overview

FrontWell Solutions is seeking a highly skilled Senior Validation Engineer to join our growing team. In this role, you will lead and execute validation projects for computerized systems and manufacturing processes in regulated environments, ensuring compliance with GMP, GLP, GxP, and GCP standards. You will play a pivotal role in modernizing quality management systems, implementing Pharma 4.0 methodologies, and driving paperless validation initiatives using leading platforms such as Kneat, Valgenesis, Polarion, DevOps, and Jira. Your expertise will help bridge the gap between regulatory requirements and digital innovation, supporting both consulting and in-house projects.

Customer Relationship Personal Evolution Autonomy Administrative Work Technical Expertise Key Responsibilities
  • Lead the planning, execution, and documentation of validation activities for computerized systems, equipment, and processes in compliance with GAMP5, CSV/CSA, and relevant regulatory standards.
  • Generate and review validation deliverables, including validation plans, user requirements, specifications, risk assessments, test protocols (IQ/OQ/PQ), and summary reports.
  • Implement and support paperless validation solutions (e.g., Kneat, Valgenesis, Polarion, DevOps, Jira), driving efficiency and data integrity in validation processes.
  • Advise on and execute strategic validation QA initiatives, including QMS modernization and adoption of new methodologies aligned with Pharma 4.0.
  • Provide quality control and QA IT support, ensuring robust compliance in pharmaceutical manufacturing and laboratory environments.
  • Collaborate with cross-functional teams, including MES/LIMS/SAP specialists, to ensure seamless integration and validation of enterprise systems.
  • Mentor and train team members and clients on validation best practices, regulatory requirements, and digital validation tools.
  • Support audits and inspections, providing expert guidance on validation documentation and compliance strategies.
Qualifications
  • Bachelor’s or Master’s degree in Engineering, Life Sciences, Computer Science, or a related field.
  • 3+ years of experience in validation engineering within the pharmaceutical, biotech, or regulated life sciences industries.
  • Deep knowledge of GMP, GLP, GxP, GCP, and GAMP5 standards, with a proven track record in computer system validation (CSV/CSA).
  • Hands-on experience with paperless validation platforms (Kneat, Valgenesis, Polarion, DevOps, Jira, Kneat GxP, Automated Testing tools).
  • Familiarity with MES, LIMS, and SAP systems as secondary skills.
  • Strong technical writing skills and experience generating validation documentation and deliverables.
  • Demonstrated ability to lead validation projects, modernize QMS, and implement new validation methodologies.
  • Excellent communication skills, with the ability to work effectively in both consulting and in-house environments.
  • Solid understanding of pharmaceutical manufacturing processes, quality control, and regulatory requirements.
Why Join FrontWell Solutions?

At FrontWell Solutions, we offer more than just a competitive salary. We are committed to fostering a transparent, supportive, and innovative work environment where your expertise is valued and your career can thrive. With us, you will benefit from:

  • Fair Work Conditions: Transparent and equitable policies for all employees.
  • Remote Work Infrastructure: Advanced tools and support for seamless remote collaboration.
  • Innovative Culture: A start-up spirit that encourages creativity, continuous learning, and the adoption of cutting-edge technologies.
  • Empowerment and Feedback: A culture built on trust, empowerment, and constructive feedback to support your personal and professional growth.
  • Career Growth: Tailored career development plans, early responsibility, and opportunities to lead impactful projects.
  • Work-Life Harmony: Flexible arrangements to support your work-life balance and personal preferences.
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