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Embedded System Validation Engineer Jobs in Minnesota

Pentangle Tech

Embedded Firmware Software Engineer

Eagan, MN · On-site

$105K - $143K/yr

... systems that monitor water and energy usage. You will work 100% onsite in Eagan, MN, collaborating closely with hardware and electrical engineers to design, build, and validate custom embedded ...

PSC Biotech

Validation Engineer

Minneapolis, MN · On-site

The Validation Engineer will collaborate with cross-functional teams to support project execution ... Support validation activities for facilities, utilities, and equipment systems. * Develop, author ...

PSC Biotech

Validation Engineer

Minneapolis, MN

The Validation Engineer will collaborate with cross-functional teams to support project execution ... Support validation activities for facilities, utilities, and equipment systems. Develop, author ...

PSC Biotech

Validation Engineer

Minneapolis, MN · On-site

$90 - $105/hr

Support validation activities for facilities, utilities, and centrifuge equipment systems ... Collaborate with Engineering, Quality, Operations, and project teams to ensure validation ...

PSC Biotech

Validation Engineer

Minneapolis, MN · On-site

$90K - $105K/yr

The Validation Engineer will collaborate with cross-functional teams to support project execution ... Support validation activities for facilities, utilities, and equipment systems. * Develop, author ...

krg technology inc

Validation Engineer

Saint Paul, MN · On-site

... system testing for medical / Non-Medical devices 3. Experience in Validation and Verification ... Requirements 1. Minimum 5-7 Years of experience in Mechanical Engineering - Degree in Mechanical ...

HTI Technology

Embedded Systems Engineer

Chanhassen, MN · On-site

$90 - $120/hr

Embedded Systems Engineer Location: Chanhassen, MN Job Id: 189 # of Openings: 1 Embedded Systems ... system integration, and validation. The ideal candidate has experience with digital and analog ...

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Embedded System Validation Engineer information

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 Minnesota?

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

What job categories do people searching Embedded System Validation Engineer jobs in Minnesota look for?

The top searched job categories for Embedded System Validation Engineer jobs in Minnesota are:

Embedded System Validation Engineer jobs near you

Computer Systems Validation Engineer

Three Point Solutions, Inc.

Maple Grove, MN • On-site

Contractor

Re-posted 22 days ago

Job description

Job Title: Computer Systems Validation Engineer
Client: Medical Device Manufacturing Company
Location: Maple Grove, MN 55311
Duration: 6 Months Contract
Focus Area: FDA-regulated Medical Device Software/Systems Validation
Position Overview
The Computer Systems Validation Engineer will be responsible for validating software and equipment in compliance with FDA regulations and company policies. This role will ensure that systems meet strict quality, compliance, and documentation standards. The ideal candidate will have strong technical expertise in validation processes, SDLC, and regulatory compliance, with experience in medical device manufacturing.
Key Responsibilities
  • Define, develop, and maintain comprehensive specifications for equipment/software (e.g., PLCs, Visual Basic apps, databases, SCADA applications, FDA-regulated systems).
  • Develop and review validation/qualification protocols, ensuring compliance with FDA requirements and QSR regulations.
  • Execute validation and qualification protocols, record results, and manage documentation via Change Requests.
  • Provide project estimates independently and review estimates for junior engineers.
  • Perform project lead activities on small to large-scale validation/qualification projects.
  • Ensure consistency and quality of validation work through peer reviews, mentoring, and training of Engineer I's and II's.
  • Support audits and regulatory inspections by providing accurate documentation and validation evidence.
  • Drive compliance with 21 CFR Part 11 (electronic records/e-signatures) and other FDA guidelines.
  • Influence cross-functional engineering initiatives and contribute to defining departmental best practices.

Required Qualifications
  • Bachelor's Degree in an Engineering discipline.
  • 5-9 years of direct experience in software/equipment validation within a regulated environment.
  • Strong background in medical device manufacturing and compliance documentation.
  • Hands-on experience with SDLC (System Development Life Cycle).
  • Excellent organizational, verbal, and written communication skills.
  • Proficiency in MS Office tools.
  • Ability to manage multiple priorities, with high attention to detail.
  • Strong interpersonal skills and a collaborative, team-oriented mindset.

Preferred Qualifications
  • Prior experience in an FDA-regulated industry.
  • Experience supporting audits and working with regulatory bodies.
  • Prior quality role experience ensuring compliance with industry standards.
  • Practical knowledge of 21 CFR Part 11 (electronic records/electronic signatures).

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