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Biomedical Design Verification Engineer Jobs (NOW HIRING)

Correct Designs

Design Verification Engineer

Austin, TX · On-site

$134K - $164K/yr

Design Verification Engineer ID: 1063 Location: Austin, TX More about this job > Description Design Verification Engineer Looking for new challenges? Would you like the variety of a contract position ...

COGENT Infotech

Design Verification Engineer

Saratoga, CA · On-site

$150K - $183K/yr

Design Verification Engineer Location: Saratoga, CA (Onsite)-5 days We are seeking a Design Verification Engineer with 8+ years of experience in semiconductor verification. The ideal candidate will ...

Correct Designs

Design Verification Engineer

Austin, TX · On-site

$134K - $164K/yr

Design Verification Engineer ID: 1058 Location: Austin, TX More about this job > Description Design Verification Engineer Looking for new challenges? Would you like the variety of a contract position ...

Texas Instruments

Design Verification Engineer

Dallas, TX · On-site

$135K - $164K/yr

Texas Instruments is seeking a Design Verification Engineer to join our Analog Power Products organization in Dallas. In this role, you will develop and execute verification strategies that ensure ...

Texas Instruments

Design Verification Engineer

Knoxville, TN · On-site

$129K - $158K/yr

Love your job. Texas Instruments is seeking a Design Verification Engineer to join our Analog Power Products organization in Knoxville. In this role, you will develop and execute verification ...

Texas Instruments Incorporated

$100K - $122K/yr

Texas Instruments is seeking a Design Verification Engineer to join our Analog Power Products organization in Dallas. In this role, you will develop and execute verification strategies that ensure ...

Texas Instruments

$126K - $154K/yr

Texas Instruments is seeking a Design Verification Engineer to join our Analog Power Products organization in Dallas. In this role, you will develop and execute verification strategies that ensure ...

Lorven Technologies

Design verification Engineer

San Jose, CA · On-site

$158K - $192K/yr

Design Verification Engineer Location: San Jose, CA We are seeking DV engineers to verify complex internal IP blocks such as compute engines, accelerators, and custom logic within SoC environments.

Normal Computing

Design Verification Engineer

New York, NY · On-site

$148K - $181K/yr

The Role As a Design Verification Engineer at Normal, you will verify our own physics-inspired ASICs on the road to tapeout, and set the quality bar for what our AI learns: reviewing generated ...

Correct Designs

Design Verification Engineer

Austin, TX · On-site

$134K - $164K/yr

Design Verification Engineer Looking for new challenges? Would you like the variety of a contract position along with long term stability and benefits? Correct Designs can give it all to you. Correct ...

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Biomedical Design Verification Engineer information

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$105.5K

$149.2K

$167K

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

As of Sep 11, 2026, the average yearly pay for biomedical design verification engineer in the United States is $149,150.00, according to ZipRecruiter salary data. Most workers in this role earn between $136,000.00 and $166,000.00 per year, depending on experience, location, and employer.

What are popular job titles related to Biomedical Design Verification Engineer jobs?

For Biomedical Design Verification Engineer jobs, the most frequently searched job titles are:

Design Verification Engineer

Chicago, IL • On-site

Ventura Solutions LLC
Medical Equipment and Supplies Manufacturing • 11 - 50 employees
Learn more about Ventura Solutions LLCexternal

$45 - $55/hr

Contractor

Medical, Dental, Retirement, PTO

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Our client is seeking an experienced Design Verification Engineer to lead the planning, development, and execution of verification activities for medical device products. This individual will serve as a technical expert in device testing, design inputs, risk analyses, and translating product requirements into robust verification strategies and test methods.
The ideal candidate possesses a strong engineering background, understands how medical devices function from both a design and user perspective, and can independently determine what testing is required to demonstrate that design requirements have been met. This role works closely with R&D, Lab, Quality, Regulatory Affairs, and external partners throughout the product development lifecycle.
Responsibilities
  • Develop and execute design verification strategies for new and existing medical devices.
  • Review product requirements, design inputs, and risk analyses to determine appropriate verification activities.
  • Create verification protocols, test plans, acceptance criteria, and reports in compliance with applicable design control requirements.
  • Ensure objective evidence is generated to demonstrate compliance with design requirements.
  • Design, develop, optimize, and validate test methods for mechanical, functional, usability, environmental, reliability, and performance testing.
  • Identify and implement appropriate measurement systems, instrumentation, fixtures, and data acquisition methods.
  • Evaluate test method capability, repeatability, and reproducibility (e.g., GR&R).
  • Develop custom test equipment and fixtures as needed.
  • Support test method validation (TMV) and testing execution.
  • Analyze test data using statistical and engineering methods.
  • Support root cause analysis and recommend corrective actions.
  • Prepare clear technical reports and present findings to project teams and management.
  • Collaborate with Design Engineering, Quality, Regulatory Affairs, and Lab staff.
  • Coordinate testing activities with external laboratories, consultants, and suppliers.
  • Mentor junior engineers and provide leadership in verification and testing practices.
  • Support overall project planning from a testing strategy perspective.
  • Ensure verification activities comply with applicable standards, guidance documents, and internal procedures.
  • Participate in Design Control, Risk Management, and Design History File (DHF) activities.
  • Apply expertise in ISO 13485 and ISO 14971.

Qualifications
  • Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Electrical Engineering, Systems Engineering, or related discipline.
  • 5 years of experience in medical device development, verification, testing, or systems engineering.
  • Demonstrated experience developing verification strategies and executing design verification programs.
  • Strong understanding of medical device design controls and product development processes.
  • Experience developing test methods and analyzing data.
  • Excellent technical writing and communication skills.
  • Ability to independently assess designs and determine appropriate verification approaches.
  • Experience with inhalation, drug delivery, combination products, surgical, diagnostic, or other complex medical devices is a plus.
  • Knowledge of risk management and failure analysis methodologies is a plus.
  • Experience with statistical analysis tools such as Minitab, JMP, or equivalent is a plus.
  • Familiarity with IEC 60601, ISO 11608, or other applicable medical device standards is a plus.
  • Experience managing external test laboratories and contract development partners is a plus.

Location
  • Chicago, IL

Employee Type
  • W2 Contract (approximately 6 months)
  • Potential for contract-to-hire conversion

Compensation & Benefits
  • Hourly rate $45-$55
  • Medical and dental insurance
  • Paid vacation time
  • 401(k) after 90 days

About Ventura Solutions
Ventura Solutions is a reputable end-to-end medical device and combination product consulting, staffing, and training firm. With our deep industry expertise spanning medical devices and combination products, coupled with an outstanding talent pool, we stand out as the preferred option for a diverse array of projects. On the consulting side, we integrate seamlessly into your team and manage small to complex Statement of Work (SOW) projects. On the staffing side, we help source, screen, and on-board reputable employees to fill temporary, temp to permanent, and permanent job openings. We accelerate product development, keep products compliant, and help build great organizations. For more information, visit us at www.ventura-solutions.com.
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