76 medical device engineer jobs at 26 companies in Berkeley, IL
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Contract Medical Device Lead Auditor
Schaumburg, Illinois, United States
FieldPart Time, Contract
4+ YOEBachelor's in science/engineering required; 4+ years quality systems and medical device experience; ISO 9001/13485 and GMP auditing experience; ability to pass a 40-hour lead auditor course; knowledge of ISO 14971 and device regulatory requirements.
3w
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Senior Device Engineer - Lifecycle Management
North Chicago, Illinois, United States
$125k-$237k/yr HybridFull Time
8+ YOE8+ years engineering experience with 5+ years embedded Windows programming in C#/.NET; medical device or regulated software experience preferred; BS or equivalent experience; strong communication and software lifecycle knowledge.
C#, .NET, RS232, SPI, USB, Microsoft Word, Microsoft Excel, IEC 62304
6d
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Field Service Engineer (Medical Device) (Orlando, FL based Field role))
Orlando or Chicago or Minneapolis or United States
$37-$63/hr FieldFull Time
2+ YOEBachelor's degree in engineering or related field, 2–5 years of technical field service experience, strong problem-solving and communication skills, technical writing ability, and travel availability up to 75%.
Salesforce (SFDC)
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Director, Program Management (Medical Device)
Buffalo Grove, Illinois, United States
$160k-$220k/yr OnsiteFull Time
10+ YOEBachelor's in Engineering/Business, 10+ years progressive program management experience in medical device/regulated manufacturing, strong leadership, stakeholder and financial management, negotiation skills, and experience with Smartsheet and Microsoft Project.
Smartsheet, Microsoft Project
1d
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Global Account Manager - Medical Device
Chicago or United States or Minnesota
$130k-$170k/yr RemoteFull Time
5+ YOEBachelor’s degree and 5+ years of medical device account management plus 5+ years of mechanical, biomedical, or related engineering experience. Requires strategic sales, negotiation, and cross-functional leadership skills.
Salesforce, Microsoft Office Suite
3w
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Senior Design Quality Engineer - Medical Devices
Carlsbad or Chicago or Raleigh or Durham or Greensboro or Pittsboro
$100k-$140k/yr HybridFull Time
5+ YOEBachelor's degree,5+ years relevant experience,knowledge of FDA 21 CFR 820/ISO 13485/ISO 14971,cGMP,GxP; experience with electromechanical devices, audits, risk management, and verification/validation.
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Sr. Principal Systems Engineer
Milwaukee or West Allis or Round Lake Beach or Skaneateles Falls
$128k-$176k/yr HybridFull Time
8+ YOEBachelor's degree in engineering or technical field and 8+ years of medical device engineering experience. Requires systems engineering, risk management, Agile SAFe, communication, and cross-functional leadership skills.
MATLAB, Azure DevOps, Polarion, TrackWise, Agile SAFe
1d
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Senior Human Factors Engineer
Northfield, Illinois, United States
$101k-$152k/yr HybridFull Time
4+ YOEBachelor’s degree in a related engineering, human factors, usability, psychology, or biomedical field and at least 4 years of human factors engineering experience; medical device experience preferred.
FDA, AAMI HE 75, ISO 62366, IEC 60601-1-6, ISO 11607-1, 21 CFR 820.30, ISO 14971
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Quality Engineer II
Kenosha, Wisconsin, United States
OnsiteFull Time
5+ YOE5+ years medical device quality engineering experience preferred; knowledge of ISO 13485, FDA 21 CFR 820, GD&T, CNC machining, EPICOR, Microsoft Office; bachelor's degree preferred.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Zoom, Microsoft Teams, EPICOR, CNC, GD&T, ASME Y14.5M
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Principal Risk Engineer
Round Lake, Illinois, United States
$112k-$154k/yr HybridFull Time
5+ YOEBachelor's in engineering, 5+ years medical device risk management/product development experience, working knowledge of ISO 14971, experience with FMEA/FTA/ hazard analysis and DOORS, strong analytical and communication skills.
ISO 14971, FMEA, FTA, DOORS
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Quality Engineer II
Kenosha, Wisconsin, United States
OnsiteFull Time
5+ YOEBachelor's preferred or equivalent, 5+ years quality engineering experience in medical device manufacturing, knowledge of ISO 13485 and FDA 21CFR 820, GD&T (ASME Y14.5), CNC and inspection experience preferred, EPICOR and Microsoft Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Zoom, Microsoft Teams, EPICOR
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Engineer II, DEV
North Barrington, Illinois, United States
$80k-$110k/yr OnsiteFull Time
2+ YOEBachelor's or master’s in biomedical/mechanical or related engineering; 2–5 years medical device experience; SolidWorks proficiency; experience with design controls, verification/validation, FMEA; project leadership and Microsoft Office skills.
SolidWorks, Microsoft Office
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Sr. Design Quality Engineer
Schaumburg, Illinois, United States
OnsiteFull Time
5+ YOEBachelor's in engineering or science (or equivalent), 5+ years quality/engineering experience, 2+ years medical device/design-control experience, knowledge of ISO 13485/14971/21 CFR 820/MDR, and ability to travel up to 25%.
1d
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Design Verification Engineer (Lab Project Specialist)
Chicago, Illinois, United States
$85k-$115k/yr OnsiteFull Time, Contract
3+ YOEBachelor's degree in engineering and 3+ years in medical device development, verification, testing, or systems engineering. Requires design controls, test methods, data analysis, technical writing, and lab or clean room work.
Minitab, JMP, GR&R, TMV, PPE, ISO 13485, ISO 14971, IEC 60601, ISO 11608
2mo
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Mechanical Design Engineer
Bloomingdale, Illinois, United States
$80k-$100k/yr OnsiteFull Time
10+ YOE10+ years in mechanical design for medical devices; SolidWorks and AutoCAD; stress analysis/FEA; FDA/ISO 13485 knowledge; design for manufacturability.
SolidWorks, AutoCAD, FEA
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Sr. Packaging Engineer, Vernon Hills, IL
Vernon Hills or Warwick
$96k-$153k/yr OnsiteFull Time
5+ YOEBachelor's in Packaging, Mechanical, Biomedical Engineering or related field; 5–8 years packaging engineering in medical device/pharma; ISO 11607-1/2, ISO 13485, ISO 16975, ICH, ASTM/ISTA; DFSS, DOE; FEA; CAPE/TOPS/SolidWorks experience.
CAPE, TOPS, SolidWorks
1mo
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Quality Engineer (Lincolnshire, IL, US, 60069)
Lincolnshire, Illinois, United States
$65k-$80k/yr OnsiteFull Time
1+ YOEBachelor's in engineering/quality/life sciences required; 1–3 years quality engineering experience in regulated/medical device environment; knowledge of QMS, FDA 21 CFR Part 820, ISO 13485; eQMS (MasterControl) and Microsoft Office proficiency; strong technical writing.
MasterControl, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
2mo
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Senior Design Assurance Quality Engineer I-II
Libertyville, Illinois, United States
$90k-$125k/yr HybridFull Time
5+ YOESenior Design Assurance Quality Engineer with medical device experience, design controls, ISO 13485, ISO 14971, FMEA, statistics, and NPD/change management.
Minitab, Statistica, Excel, SAP, HRIS
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Quality Engineer I
Chicago, Illinois, United States
HybridFull Time
4+ YOEBachelor's preferred or 4+ years in medical device/pharmaceutical production, experience with ISO 13485 and CFR Part 820, regulatory inspections, and CAPA; strong critical thinking and independent work skills.
2mo
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Senior/Principal Engineer or Scientist, Combination Products
Bern or Munich or Switzerland or Research Triangle Park or Boston or Chicago or Philadelphia or New Jersey
HybridFull Time
8+ YOEMinimum 8+ years in medical device, pharmaceutical, or combination product industries, bachelor's in engineering or science required, subject matter expertise in combination products, technical leadership and client-facing experience.
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