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Embedded System Validation Engineer Jobs in Lexington, MA

United Airlines

Embedded Test Engineer

Burlington, MA · On-site

$54K - $108K/yr

... for embedded systems validation Perform functional, regression, and system-level testing on ... developers to identify and resolve defects Document test procedures, results, and technical ...

Apple

Silicon Validation Engineer

Waltham, MA

$116K - $203K/yr

... validation of various analog & mixed signal embedded circuits; and collaborate with multi ... Hands on SerDes Lab experience Python programming experience Minimum Qualifications Bachelors ...

Apple

Silicon Validation Engineer

Waltham, MA

$165K - $292K/yr

... validation of various analog & mixed signal embedded circuits; and collaborate with multi ... Hands on SerDes Lab experience Python programming experience Minimum Qualifications BSEE and 10+ ...

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All JobsEmbedded System Validation Engineer JobsEmbedded System Validation Engineer Jobs in Lexington, MA

Embedded System Validation Engineer information

See Lexington, MA salary details

$70.2K

$154.2K

$215.7K

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

As of Sep 3, 2026, the average yearly pay for embedded system validation engineer in Lexington, MA is $154,233.00, according to ZipRecruiter salary data. Most workers in this role earn between $125,300.00 and $183,700.00 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 are popular job titles related to Embedded System Validation Engineer jobs in Lexington, MA?

For Embedded System Validation Engineer jobs in Lexington, MA, the most frequently searched job titles are:

What job categories do people searching Embedded System Validation Engineer jobs in Lexington, MA look for?

The top searched job categories for Embedded System Validation Engineer jobs in Lexington, MA are:

What cities near Lexington, MA are hiring for Embedded System Validation Engineer jobs?

Cities near Lexington, MA with the most Embedded System Validation Engineer job openings:

Embedded System Validation Engineer jobs near you
Infographic showing various Embedded System Validation Engineer job openings in Lexington, MA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, and 4% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $154,233 per year, or $74.2 per hour.

Sr Engineer Computer Systems Validation

Scorpion Therapeutics

Harvard, MA • On-site

$99 - $121/hr

Other

Medical, PTO

Posted 4 days ago

Job description

Position Summary

The Senior Engineer, IT Compliance and CSV supports computerized system validation, IT compliance, and change/deviation management for regulated computerized systems across the Devens Campus (including the Cell Therapy Facility). Executes System Life Cycle deliverables; serves as a CSV SME; supports IT Deviation Management, Computer System Audit, Change Management, and Risk Management programs; works with Quality, Validation, Manufacturing, Engineering, and enterprise teams.

Duties/Responsibilities
  • Execute CSV and IT compliance activities (including for Devens CTF) aligned to team/site objectives.
  • Serve as CSV SME for computerized system changes and related IT/Automation projects; advise operations.
  • Support IT Deviation Management, Computer System Audit, Change Management, and Risk Management programs.
  • Guide Digital Plant/site groups on CSV process implementation; analyze/address process deficiencies.
  • Support Data Integrity and Quality Risk Management programs.
  • Provide IT quality support: review/approve investigations and change controls; own computerized system events and CSV activities.
  • Enter/support deviations, actions, root cause analysis, CAPA, and effectiveness reviews in the Quality Management System.
  • Participate in regulatory/internal audits and inspections; respond to audit observations.
  • Implement/track Service Level Agreements (SLAs) for business-critical activities.
  • Develop/maintain GxP procedures and guidance for compliance and audit readiness.
  • Execute validation/implementation/change management for regulated IT systems.
  • Track project progress; provide updates via tools/dashboards.
  • Improve efficiency/quality of CSV documentation and processes; evaluate technologies/tools/process improvements.
Qualifications
  • Bachelor’s degree (Engineering/Science/IT or related IT/OT), 3–5 years relevant Compliance and CSV experience (preferably Cell Therapy/Biologics Manufacturing).
  • Knowledge of regulatory CSV requirements (FDA/EMA; e.g., ICH Q7/Q8/Q9).
  • Working knowledge: 21 CFR Part 11; 21 CFR Parts 210/211; GAMP (ISO 9001 is a plus).
  • Working knowledge of health authority/digital asset requirements incl. Data Integrity.
  • Experience with quality systems, risk management, audit readiness, deviation and change management in regulated automated manufacturing.
  • Ability to represent department to stakeholders and regulatory agencies.
  • Ability to support US FDA and other agency interactions.
  • Strong project management, communication, and technical writing; training experience is a plus.
  • Lean Six Sigma and OPEX understanding.
  • Ability to innovate, synthesize cross-functional solutions, collaborate, and manage multiple priorities.
  • Internal audit/inspection experience advantageous.
  • Willingness to mentor and share knowledge.
Compensation/Benefits
  • Devens, MA: $99,480–$120,551 (full-time). Additional incentive cash/stock may be available (eligibility-based).
  • Benefits include health coverage, wellbeing support, and financial protection; work-life benefits include Paid Time Off (specific to role/location).
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