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Embedded System Validation Engineer Jobs in Indiana

cillium corp

Embedded Software Engineer

Michigan City, IN · On-site

$127K - $168K/yr

Clint seeking an Embedded Software Engineer to participate in the development of Silvus ... Linux system customization and scripting. Qualifications: Expert in C programming. Other language ...

ITW Avery Weigh-Tronix

Embedded Software Engineer

IN · On-site

$125K - $165K/yr

... • Validate successive software versions to ensure proper integration with system hardware. • ... in embedded programming languages (e.g., C/C++), version control (Git/Github) and real-time ...

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Embedded System Validation Engineer information

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 Embedded System Validation Engineers?

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.
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Embedded System Validation Engineer jobs near you
6095 - CQV Engineer / Validation Engineer

6095 - CQV Engineer / Validation Engineer

Verista, Inc.

Bloomington, IN

Other

Re-posted 2 days ago

Job description

CQV / Validation Engineer Responsibilities:Commissioning, Qualification & Validation (CQV)
  • Execute commissioning, qualification, and validation activities for manufacturing equipment, utilities, facilities, and process systems.
  • Author, review, and execute validation lifecycle documentation including:
    • Commissioning Protocols
    • IQ (Installation Qualification)
    • OQ (Operational Qualification)
    • PQ (Performance Qualification)
    • Validation Summary Reports
    • Traceability Matrices
    • Risk Assessments
  • Support startup and operational readiness activities for new production equipment and manufacturing systems.
  • Perform field verification activities, walkdowns, and documentation reviews to ensure systems are installed and functioning according to design requirements.
  • Coordinate testing activities with Engineering, Manufacturing, Quality, and Vendor teams.
Manufacturing & Technical Support
  • Support qualification of production equipment used in pharmaceutical manufacturing operations.
  • Troubleshoot qualification and validation issues encountered during equipment startup and testing.
  • Review engineering documentation including P&IDs, equipment specifications, drawings, and vendor documentation.
  • Ensure equipment and systems meet GMP, regulatory, and internal quality requirements.
  • Assist in identifying and resolving deviations, discrepancies, and validation-related issues.
Compliance & Documentation
  • Ensure all validation activities are executed in accordance with current GMP regulations and company procedures.
  • Maintain clear, accurate, and compliant validation documentation.
  • Support change controls, deviations, CAPAs, and validation impact assessments as required.
  • Participate in audits and inspections by providing validation subject matter expertise.
Lead Validation Engineer (Additional Responsibilities)
  • Provide technical leadership and mentorship to validation team members.
  • Coordinate validation deliverables and execution schedules across multiple systems and workstreams.
  • Interface with project leadership to communicate risks, resource needs, and project status.
  • Review and approve validation documentation prepared by junior team members.
  • Drive resolution of complex qualification and startup challenges.
Requirements:
  • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline.
  • 3+ years of CQV, Validation, Commissioning, or Qualification experience (Validation Engineer).
  • 7+ years of CQV, Validation, or Pharmaceutical Manufacturing experience (Lead Validation Engineer).
  • Experience supporting GMP-regulated pharmaceutical, biotech, medical device, or manufacturing environments.
  • Strong understanding of validation lifecycle principles and documentation requirements.
  • Experience authoring and executing IQ/OQ/PQ protocols.
  • Ability to work onsite in Bloomington, Indiana.
Preferred
  • Experience supporting startup of new manufacturing lines, facilities, or capital projects.
  • Experience within pharmaceutical manufacturing, sterile manufacturing, biologics, or contract manufacturing environments.
  • Familiarity with ISPE, FDA, EU GMP, and GAMP guidance.
  • Experience managing deviations, change controls, and risk assessments.
  • Strong technical writing and documentation skills.
Key Skills
  • Commissioning & Qualification (CQV)
  • Equipment Validation
  • Manufacturing Systems
  • IQ / OQ / PQ Execution
  • GMP Compliance
  • Technical Writing
  • Risk Assessments
  • Deviation Management
  • Change Control
  • Cross-Functional Collaboration
  • Startup & Operational Readiness
  • Problem Solving & Troubleshooting

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