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Medical Device R&D Jobs in Chicago, IL (NOW HIRING)

Intellectt INC

Controls Engineer

Libertyville, IL · On-site

$81K - $105K/yr

Medical device manufacturing experience. * Experience with Keyence / FANUC vision systems. * Experience with Beckman or B&R (ABB) PLCs. Thanks & Regards, Vyshnavi Recruiter Intellectt Inc vyshnavi.t ...

Med-Stat Consulting Services, Inc.

Be Seen First

Biomedical Technician - Hospital

Chicago, IL · On-site

$28 - $36/hr

Full-time position with top-rated benefits, including health/vision/dental, AD&D, and 401k with ... Company Description Med+Stat is a national medical device service company with a specialty focus on ...

Lancesoft

Engineer

Gary, IN · On-site

$35 - $43/hr

... R, etc.) Knowledge of the Medical Device Industry and familiarity with FDA QSR Regulations - preferred Proficiency in SolidWorks. Mechanical understanding, tool design experience Technical writing ...

Actalent

Document Control Specialist

Winnetka, IL

$30/hr

Experience working in the medical device industry. * Knowledge of cGMP and GDP requirements in a ... AD&D for the employee and dependents) • Short and long-term disability • Health Spending ...

New

Med-Stat Consulting Services, Inc.

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Field Service Technician - Hospital

Chicago, IL · On-site

$24 - $32/hr

Full-time position with top-rated benefits, including health/vision/dental, AD&D, and 401k with ... Company Description Med+Stat is a national medical device service company with a specialty focus on ...

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All JobsMedical Device R&D JobsMedical Device R&D Jobs in Chicago, IL

Medical Device R D information

See Chicago, IL salary details

$22

$51

$99

How much do medical device r&d jobs pay per hour?

As of Jun 12, 2026, the average hourly pay for medical device r&d in Chicago, IL is $51.34, according to ZipRecruiter salary data. Most workers in this role earn between $36.15 and $61.39 per hour, depending on experience, location, and employer.

What is a Medical Device R&D job?

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 are the typical daily responsibilities of someone working in Medical Device R&D?

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 the Medical Device R&D position, and why are they important?

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 Chicago, IL? For Medical Device R&D jobs in Chicago, IL, the most frequently searched job titles are:
What job categories do people searching Medical Device R&D jobs in Chicago, IL look for? The top searched job categories for Medical Device R&D jobs in Chicago, IL are:
Medical Device R D jobs near you
Infographic showing various Medical Device R&D job openings in Chicago, IL as of June 2026, with employment types broken down into 90% Full Time, 1% Part Time, 8% Contract, and 1% Nights. Highlights an 92% Physical, 4% Hybrid, and 4% Remote job distribution, with an average salary of $106,787 per year, or $51.3 per hour.
Validation Engineer/Quality Systems Engineer

Validation Engineer/Quality Systems Engineer

Jacobs Management Group

Vernon Hills, IL

$90K - $100K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 9 days ago

Job description

My client is a medical device company seeking a Validation Engineer to own the full validation lifecycle - from writing and executing protocols to maintaining the calibration system and supporting regulatory compliance. This role sits at the intersection of Quality Systems and engineering, and is central to the company's ability to bring compliant, high-quality products to market.

Why You Should Apply

  • Broad scope - own validation, calibration, and quality systems work across the organization
  • Direct impact on regulatory compliance for a growing medical device company
  • Cross-functional visibility - partner with engineering, manufacturing, and quality leadership
  • Salary range: $90,000 - $100,000
  • Full benefits package including medical, dental, vision, and 401k

What You'll Be Doing

  • Write, execute, and maintain validation protocols for manufacturing equipment, processes, and systems
  • Manage the calibration system and equipment database
  • Analyze validation data and identify nonconformities; recommend and track corrective actions
  • Support design controls, CAPA, change control, and post-market surveillance activities
  • Review DHF deliverables and provide FDA compliance guidance

About You

  • Be able to do the job as described
  • Knowledge of ISO 13485, ISO 14971, 21 CFR Part 820, and EU-MDR
  • Experience with process and test method validations in an FDA-regulated industry
  • Background in medical device or pharmaceutical manufacturing
  • Blow-Fill-Seal experience is a plus

This is a full-time, permanent direct-hire opportunity. My client is unable to provide visa sponsorship now or in the future. Applicants must be authorized to work in the United States without sponsorship.

How To Apply

We'd love to see your resume, but we don't need it to have a conversation. Email Cat at ccupo@jacobsmgt.com and tell me why you're interested. Or, if you do have a resume ready, apply here.