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Biomedical Engineering Consulting Jobs in Illinois

Advocate Aurora Health

... after consultation with charge person. 4)Accurate records of repairs and maintenance are kept per policy. 5)Communicates with the Biomedical Engineering department when repairs of endoscopes are ...

Advocate Aurora Health

Endoscopy tech 1

Des Plaines, IL

$20.80 - $31.20/hr

... after consultation with charge person. 4)Accurate records of repairs and maintenance are kept per policy. 5)Communicates with the Biomedical Engineering department when repairs of endoscopes are ...

Advocate Aurora Health

Endoscopy tech 1

Park Ridge, IL · On-site

$20.80 - $31.20/hr

... after consultation with charge person. 4)Accurate records of repairs and maintenance are kept per policy. 5)Communicates with the Biomedical Engineering department when repairs of endoscopes are ...

Pwc

Kinaxis Solutions Architect, Manager

Chicago, IL

$99K - $232K/yr

... Operations Consulting practice. You will work closely with clients to analyze supply chain ... Aerospace Engineering, Automotive Engineering, Biomedical Engineering, Chemical Engineering ...

Pwc

Supply Chain Execution Manager

Chicago, IL · On-site

$99K - $232K/yr

Within our Operations Consulting practice, you will focus on optimizing supply chain footprints ... Aerospace Engineering, Automotive Engineering, Biomedical Engineering, Chemical Engineering ...

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Showing results 21-40

All JobsBiomedical Engineering Consulting JobsBiomedical Engineering Consulting Jobs in Illinois

Biomedical Engineering Consulting information

See Illinois salary details

$39.7K

$91.9K

$135.7K

How much do biomedical engineering consulting jobs pay per year?

As of Aug 23, 2026, the average yearly pay for biomedical engineering consulting in Illinois is $91,870.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,200.00 and $112,400.00 per year, depending on experience, location, and employer.

What is biomedical engineering consulting?

Biomedical engineering consulting involves providing expert advice and solutions related to the design, development, and implementation of medical devices, healthcare technologies, and related systems. Consultants in this field help organizations navigate regulatory requirements, improve product designs, troubleshoot technical issues, and ensure compliance with industry standards. They often work with hospitals, medical device companies, and research institutions to optimize processes and bring innovative products to market safely and efficiently.

How do biomedical engineering consultants typically collaborate with clients and multidisciplinary teams during a project?

Biomedical engineering consultants frequently work alongside clients such as hospitals, medical device companies, or research institutions, as well as multidisciplinary teams including clinicians, regulatory specialists, and product designers. Effective collaboration often involves participating in regular meetings, clarifying technical requirements, and translating complex engineering concepts for non-technical stakeholders. Consultants also coordinate project timelines, ensure compliance with industry regulations, and provide ongoing technical support throughout the product development or implementation process. Building strong communication and project management skills is essential for thriving in this collaborative environment.

What are the key skills and qualifications needed to thrive as a biomedical engineering consultant, and why are they important?

To thrive as a Biomedical Engineering Consultant, you need a solid background in biomedical engineering principles, regulatory standards, and a relevant degree, often at the bachelor’s or master’s level. Familiarity with industry-standard tools such as CAD software, statistical analysis programs, and a working knowledge of medical device regulations (like FDA or ISO standards) is crucial. Strong problem-solving skills, effective communication, and the ability to collaborate with multidisciplinary teams set top consultants apart. These skills are vital to ensure innovative, compliant solutions and successful client outcomes in a complex and regulated field.

What is the difference between Biomedical Engineering Consulting vs Biomedical Equipment Technician?

AspectBiomedical Engineering ConsultingBiomedical Equipment Technician
CredentialsBiomedical engineering degree, certifications like CBET or BIETAssociate or bachelor's in biomedical technology, CBET certification
Work EnvironmentConsulting firms, hospitals, medical device companiesHospitals, clinics, service centers
Employer & IndustryConsulting firms, healthcare, medical device industryHealthcare facilities, medical equipment service providers
Job FocusDesign, development, regulatory compliance, project managementMaintenance, repair, calibration of medical equipment

While both roles involve medical devices, Biomedical Engineering Consulting focuses on design, development, and advising on medical systems, whereas Biomedical Equipment Technicians primarily handle maintenance and repair of equipment on-site.

What does a biomedical engineering consulting do?

A biomedical engineering consulting professional provides expertise in designing, evaluating, and improving medical devices, equipment, and systems. They often analyze clinical needs, ensure regulatory compliance, and apply engineering principles to develop innovative healthcare solutions, typically working with cross-disciplinary teams and utilizing tools like CAD software. Their work supports hospitals, medical device companies, and research institutions to enhance patient care and safety.

What are popular job titles related to Biomedical Engineering Consulting jobs in Illinois?

For Biomedical Engineering Consulting jobs in Illinois, the most frequently searched job titles are:

What job categories do people searching Biomedical Engineering Consulting jobs in Illinois look for?

The top searched job categories for Biomedical Engineering Consulting jobs in Illinois are:

What cities in Illinois are hiring for Biomedical Engineering Consulting jobs?

Cities in Illinois with the most Biomedical Engineering Consulting job openings:

Biomedical Engineering Consulting jobs near you
Infographic showing various Biomedical Engineering Consulting job openings in Illinois as of August 2026, with employment types broken down into 80% Full Time, 6% Part Time, and 14% Contract. Highlights an 90% In-person, 3% Hybrid, and 7% Remote job distribution, with an average salary of $91,870 per year, or $44.2 per hour.

Design Verification Engineer

Ventura Solutions LLC

Chicago, IL • On-site

$45 - $55/hr

Contractor

Medical, Dental, Retirement, PTO

Re-posted yesterday

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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