Design Verification Engineer

Job Description

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.
• 3-5 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

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