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Medical Device R&D Jobs in Illinois (NOW HIRING)

Nemera

Laboratory Project Specialist

Chicago, IL · On-site

Evaluate test method capability, repeatability, and reproducibility (e.g., GR&R). * Develop custom ... Strong understanding of medical device design controls and product development processes.

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Medical Device R D information

What is a medical device R&D?

A Medical Device R&D job involves researching, designing, and developing new medical devices or improving existing ones. Professionals in this role collaborate with engineers, scientists, and regulatory experts to ensure products meet safety, efficacy, and regulatory standards. They conduct feasibility studies, prototyping, and testing to refine device functionality before commercial production. The role requires a strong understanding of engineering principles, biomedical sciences, and regulatory compliance.

What does a medical device R&D do?

Professionals in Medical Device R&D spend their days designing and prototyping new medical devices, conducting experiments to test functionality and safety, and collaborating closely with cross-functional teams such as manufacturing, clinical affairs, and regulatory specialists. They often work on troubleshooting design challenges, documenting progress, and ensuring their work complies with strict regulatory standards. Regular meetings, technical reviews, and hands-on testing in labs are common, making the environment both collaborative and fast-paced. This role is ideal for individuals who enjoy creative problem-solving and have a passion for improving medical technology.

What are the key skills and qualifications needed to thrive in medical device R&D?

To excel in Medical Device R&D, you typically need a degree in biomedical engineering or a related field, strong problem-solving abilities, and knowledge of regulatory standards such as FDA or ISO. Experience with CAD software, rapid prototyping tools, and quality management systems is highly valuable, along with certifications like Six Sigma or PMP for project management. Strong teamwork, attention to detail, and effective communication skills set candidates apart. These competencies are essential to innovate, ensure compliance, and deliver safe, effective medical devices in a highly regulated industry.

What are popular job titles related to Medical Device R&D jobs in Illinois?

For Medical Device R&D jobs in Illinois, the most frequently searched job titles are:

What job categories do people searching Medical Device R&D jobs in Illinois look for?

The top searched job categories for Medical Device R&D jobs in Illinois are:

What cities in Illinois are hiring for Medical Device R&D jobs?

Cities in Illinois with the most Medical Device R&D job openings:

Medical Device R D jobs near you
Infographic showing various Medical Device R&D job openings in Illinois as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Design Verification Engineer

Ventura Solutions LLC

Chicago, IL • On-site

$45 - $55/hr

Contractor

Medical, Dental, Retirement, PTO

Posted 25 days ago

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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