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Freelance Design Verification Engineer Jobs in Fishers, IN

Design verification and validation test plans and protocols * Analyze testing data and recommend ... Create engineering procedures, work instructions, and standardized processes * Support design ...

Design Engineer

Indianapolis, IN · On-site

$100K - $110K/yr

Design verification and validation test plans and protocols * Analyze testing data and recommend ... Create engineering procedures, work instructions, and standardized processes * Support design ...

These efforts will be effectively employed alongside the Project Engineer, Validation and Verification Engineer, and program design and functional chiefs. * Perform technical analysis of thermo-fluid ...

These efforts will be effectively employed alongside the Project Engineer, Validation and Verification Engineer, and program design and functional chiefs. * Perform technical analysis of thermo-fluid ...

Conduct post-construction reviews to verify that all applicable engineering and construction standards have been met and that installed work matches design specifications. * Perform root cause ...

Design Engineer

Carmel, IN · Hybrid

$29.81/hr

Conduct post-construction reviews to verify that all applicable engineering and construction standards have been met and that installed work matches design specifications. * Perform root cause ...

Design Engineer

Indianapolis, IN · On-site

$65K - $85K/yr

Conduct site visits, field investigations, and data collection to inform design and verify existing ... Engineer-in-Training (EIT) certification preferred * Experience with design and analysis tools ...

Conduct site visits, field investigations, and data collection to inform design and verify existing ... Engineer-in-Training (EIT) certification preferred * Experience with design and analysis tools ...

Prepare, review, and verify engineering calculations, reports, and technical documentation ... Revit design proficiency * Ability to work in a fast paced environment * Ability to coordinate ...

Prepare, review, and verify engineering calculations, reports, and technical documentation ... Revit design proficiency * Ability to work in a fast paced environment * Ability to coordinate ...

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Freelance Design Verification Engineer information

See Fishers, IN salary details

$98.7K

$139.6K

$156.3K

How much do freelance design verification engineer jobs pay per year?

As of Aug 24, 2026, the average yearly pay for freelance design verification engineer in Fishers, IN is $139,605.00, according to ZipRecruiter salary data. Most workers in this role earn between $127,300.00 and $155,400.00 per year, depending on experience, location, and employer.

What is the difference between Freelance Design Verification Engineer vs Freelance Hardware Test Engineer?

AspectFreelance Design Verification Engineer

Freelance Design Verification Engineers focus on verifying that hardware designs meet specifications through simulation and testing, often working on FPGA, ASIC, or semiconductor projects. They typically hold certifications in digital design and verification tools, and work in industries like semiconductor, electronics, and tech startups. Freelance Hardware Test Engineers, on the other hand, primarily perform physical testing of hardware prototypes and products, focusing on functional and reliability testing in manufacturing environments. While both roles require technical expertise, verification engineers emphasize simulation and design validation, whereas test engineers focus on real-world hardware testing.

What are popular job titles related to Freelance Design Verification Engineer jobs in Fishers, IN?

For Freelance Design Verification Engineer jobs in Fishers, IN, the most frequently searched job titles are:

Design Quality Engineer

Indianapolis, IN • On-site

Prophecy Technologies
11 - 50 employees

Full-time

Posted 27 days ago


Job description

Design Quality Engineer
Technical/Functional
Skills • Strong understanding of Medical Device Product Development Process and Design Control requirements. • Knowledge of FDA 21 CFR Part 820, ISO 13485, ISO 14971, and applicable regulatory standards. • Strong knowledge of Design Controls and medical device product development. • Experience with Design History File (DHF) development, review, and remediation.
• Hands-on experience with Risk Management activities including: o dFMEA o uFMEA o Preliminary Hazard Analysis (PHA) o Hazard Analysis • Knowledge of FDA 21 CFR Part 820, ISO 13485, and ISO 14971. • Experience with Design Verification and Validation (V&V). • Understanding of User Needs, Design Inputs, Design Outputs, and Traceability requirements. • Experience preparing and reviewing: o Product Specification Documents (PSD) o Product Characterization documents o CTQ (Critical-to-Quality) documents • Experience with CAPA, Nonconformance, and root cause investigations. • Familiarity with PLM systems such as Windchill, or Teamcenter. • Experience with Cockpit Cognition DHF Build and DHF traceability management. • Strong documentation, technical writing, and audit support skills.
Roles & Responsibilities • Support quality activities throughout the product development lifecycle. • Review and maintain Design History File (DHF) documentation for compliance with regulatory and quality requirements. • Lead and support risk management activities including dFMEA, uFMEA, and PHA updates. • Ensure traceability between User Needs, Design Inputs, Risk Controls, Verification, Validation, and Design Outputs. • Support Design Verification and Validation planning, execution, and documentation reviews. • Review Product Characterization, Product Specification (PSD), and CTQ documents. • Participate in design reviews and ensure compliance with
Design Control processes. • Support Cockpit Cognition DHF Build activities, including documentation organization and traceability linkages. • Conduct DHF gap assessments and support remediation activities. • Collaborate with R&D, Manufacturing, Regulatory Affairs, and Supplier Quality teams. • Support CAPA investigations, root cause analysis, and implementation of corrective actions. • Ensure compliance with FDA, ISO 13485, ISO 14971, and internal quality procedures. • Support internal audits, customer audits, and regulatory inspections. • Drive continuous improvement initiatives related to design quality and risk management processes.