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Medical Device Engineer Jobs in Chicago, IL (NOW HIRING)

Del Medical, Inc.

Assembler

Bloomingdale, IL · On-site

$19 - $22/hr

Del Medical, Inc. is a leading company in the medical device manufacturing industry. We're looking ... Read and understand Engineering Blueprints and instructions to put together medical products ...

New

Ventura Solutions LLC

Sales Engineer

Barrington, IL · On-site +1

We are seeking a dynamic and results-driven Medical Device Sales Engineer to drive the growth of our consulting, staffing, and training services. The ideal candidate will have a solid background in ...

Ventura Solutions LLC

Sales Engineer

Barrington, IL · On-site

We are seeking a dynamic and results-driven Medical Device Sales Engineer to drive the growth of our consulting, staffing, and training services. The ideal candidate will have a solid background in ...

Adecco

2nd Shift Catheter Operator

Wheeling, IL · On-site

$19.50/hr

Medical Device Catheter Assembler/Operator - 2nd Shift ???? Shift: Monday - Friday, 3:00pm-11:20pm ???? Pay Rate: $19.50 per hour Start a Career in the Medical Device Industry Are you detail-oriented ...

Sterling Engineering Inc.

Quality Engineer

Chicago, IL · Hybrid

$45 - $60/hr

Build the Validation Strategy for a New Medical Device Program We're seeking a hands-on Quality Engineer to support the launch of a new assembly program for drug delivery devices. This is a unique ...

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All JobsMedical Device Engineer JobsMedical Device Engineer Jobs in Chicago, IL

Medical Device Engineer information

See Chicago, IL salary details

$22

$51

$99

How much do medical device engineer jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for medical device engineer in Chicago, IL is $51.38, according to ZipRecruiter salary data. Most workers in this role earn between $36.20 and $61.44 per hour, depending on experience, location, and employer.

What does a medical device engineer do?

A Medical Device Engineer is responsible for designing, developing, testing, and improving medical devices used in healthcare settings. They work closely with doctors, scientists, and regulatory bodies to ensure that devices are safe, effective, and compliant with industry standards. Their work includes creating prototypes, conducting risk assessments, and overseeing the manufacturing process. Medical Device Engineers play a crucial role in bringing innovative technologies to market that help diagnose, treat, or monitor medical conditions.

What does a medical device engineer do?

A medical device engineer is an engineering professional who develops new medical equipment and medical devices. As a medical device engineer, your work will vary depending on your area of expertise and may include biomedical research, material research and sourcing, computer-aided design work, and teaming up with doctors and patients. You also must understand the manufacturing process and ensure the products you design are both useful and cost-effective. You look for innovative solutions to medical problems and design new equipment diagnoses and treatments.

What are the key skills and qualifications needed to thrive as a medical device engineer, and why are they important?

To thrive as a Medical Device Engineer, you need a solid background in biomedical, mechanical, or electrical engineering, often supported by a relevant bachelor's or master's degree. Familiarity with CAD software, regulatory standards (such as FDA or ISO 13485), and design validation tools is typically required. Strong problem-solving, communication, and teamwork skills are essential for collaborating on multidisciplinary projects and ensuring product safety. These competencies are crucial for developing innovative, compliant devices that improve patient outcomes and meet rigorous industry standards.

What are some common challenges medical device engineers face when bringing a new product from concept to market?

Medical Device Engineers often encounter challenges such as navigating complex regulatory requirements, ensuring product safety and efficacy, and coordinating with cross-functional teams including design, manufacturing, and quality assurance. Balancing innovation with compliance, managing timelines, and addressing unforeseen technical issues are also typical hurdles. Successful engineers leverage strong project management and communication skills to collaborate effectively and bring devices to market efficiently.

What is the difference between Medical Device Engineer vs Biomedical Engineer?

AspectMedical Device EngineerBiomedical Engineer
CredentialsBachelor's or Master's in Engineering, certifications in medical device designBachelor's or Master's in Biomedical Engineering or related field
Work EnvironmentDesign, develop, test medical devices in labs or manufacturing settingsResearch, develop medical equipment, or work in clinical settings
Industry UsagePrimarily in medical device manufacturing companiesHospitals, research institutions, medical device companies

Medical Device Engineers focus on designing and testing specific medical devices, ensuring compliance and safety. Biomedical Engineers have a broader scope, working on medical equipment, implants, and research. Both roles require similar credentials and often overlap in industry settings, but their primary focus differs.

More about Medical Device Engineer jobs

What are the most commonly searched types of Medical Device Engineer jobs in Chicago, IL?

The most popular types of Medical Device Engineer jobs in Chicago, IL are:

What are popular job titles related to Medical Device Engineer jobs in Chicago, IL?

For Medical Device Engineer jobs in Chicago, IL, the most frequently searched job titles are:

What job categories do people searching Medical Device Engineer jobs in Chicago, IL look for?

The top searched job categories for Medical Device Engineer jobs in Chicago, IL are:

What cities near Chicago, IL are hiring for Medical Device Engineer jobs?

Cities near Chicago, IL with the most Medical Device Engineer job openings:

Medical Device Engineer jobs near you
Infographic showing various Medical Device Engineer job openings in Chicago, IL as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 15% Part Time, and 5% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $106,871 per year, or $51.4 per hour.

DDT Medical Device Investigation Analyst

Takeda Pharmaceutical Company Limited

Bannockburn, IL • On-site

$89K - $141K/yr

Full-time

Posted 8 days ago

Takeda Pharmaceuticals rating

7.3

Company rating: 7.3 out of 10

Based on 71 frontline employees who took The Breakroom Quiz

70th of 86 rated pharmaceutical

Job description

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
About the Role:
The DD&T US Medical Device Investigation Analyst, reporting to the Plasma-Derived Therapies (PDT) DD&T Operations Lead, is responsible for leading, coordinating, and documenting investigations related to Takeda-developed and owned software and connected medical devices used within U.S. PDT and BioLife operations. This role ensures that device-related complaints, incidents, and quality events are investigated in a timely, compliant, and inspection-ready manner in accordance with FDA Quality System Regulations and Medical Device Reporting (MDR) requirements.
Working closely with DD&T, Quality, Medical Affairs, and Operations, the analyst identifies root causes, assesses potential patient and donor risk, and ensures appropriate linkage to MDRs, deviations, CAPAs, and continuous improvement initiatives. The role plays a critical part in maintaining product quality, regulatory compliance, and operational excellence across the PDT and BioLife network.
How You Contribute:
  • Manage end-to-end software medical device complaint intake, investigation, and closure, ensuring FDA/QMS compliance and on-time processing.
  • Triage issues (including ServiceNow IT tickets) to determine complaint applicability, regulatory impact, and donor safety, eligibility, and data integrity risk.
  • Execute FDA-ready investigations proportional to complaint significance, producing complete, defensible, inspection-ready records.
  • Reproduce defects in qualified environments and analyzed application code, system logs, database data, and release artifacts to identify probable root cause.
  • Document root cause or most probable cause with objective evidence and clear rationale when definitive conclusions were not possible.
  • Link complaints to releases, builds, and change controls, ensuring full traceability across quality records.
  • Author clear, concise complaint narratives in TrackWise, preserving reporter intent and supporting conclusions with complete evidence.
  • Partner cross-functionally with Support, Product, and US based Regulatory and Quality teams to guide investigations and drive timely, compliant resolution.
  • Create, review, and develop mitigation process and procedures for all identified complaints that have compliance risk without an immediate final resolution.
  • Support MDR reportability assessments by providing investigation findings, timelines, and technical input in accordance with FDA 21 CFR Part 803 requirements for software devices.
  • Participate in audit responses related to device investigations, complaints, and MDR activities. Participate in-person for all US based audits.
  • Identify trends and contribute to continuous improvement of investigation processes and metrics.
  • Provide required reporting on all DDT-related compliance activities including Complaint and quality record timeliness and department training.
  • Work cross-functionally to incorporate AI and advanced reporting into all DDT compliance activities.
  • Ensure all DDT teams are adequately training on quality related compliance activities.

Minimum Requirements/Qualifications:
  • Bachelor's degree in computer science, Life Sciences, Quality, or related technical discipline.
  • 2-5 years of experience in medical device investigations, quality assurance, complaint handling, or regulated IT/healthcare environments.
  • Working knowledge of medical device quality system requirements (FDA QSR, ISO 13485 concepts).
  • Experience performing root cause analysis and documenting regulated investigations.
  • Strong written documentation and cross-functional communication skills.
  • Basic knowledge of SQL and at least one programming language.
  • Investigation ownership and critical thinking
  • Risk-based decision making
  • High-quality technical documentation
  • Cross-functional collaboration in regulated environments
  • Regulatory and compliance mindset

Preferred:
  • Experience with software as a medical device (SaMD) or digital health platforms.
  • Familiarity with FDA MDR (21 CFR Part 803) and post-market surveillance support activities.
  • Experience working in plasma collection, biotech, or highly regulated operational environments.
  • Prior support of FDA inspections or quality audits.
  • Experience with Power BI (including building reports and dashboards).

Takeda Compensation and Benefits Summary
We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices.
For Location:
Bannockburn, IL
U.S. Base Salary Range:
$89,900.00 - $141,240.00
The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location.
For information about our benefits, please click here.
EEO Statement
Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law.
Locations
Bannockburn, ILCambridge, MA, Exton, PA
Worker Type
Employee
Worker Sub-Type
Regular
Time Type
Full time
Job Exempt
Yes

What Takeda Pharmaceuticals employees say

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Benefits

Hours and flexibility

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About Takeda Ventures

Sourced by ZipRecruiter

Industry

Investment clubs and venture capital companies, pharmaceutical product wholesalers and pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

San Diego, CA, US

Social media

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