151 device engineer jobs at 53 companies in Volo, IL
1d
Save
Mark Applied
Hide
Sr Engineer, Emerging Device Technology
North Chicago or South San Francisco or Irvine or Germany
$97k-$184k/yr OnsiteFull Time
8+ YOEBS, MS, or PhD in engineering; 12 years with BS or 8 years with MS/MBA; medical device and drug delivery experience; design control and combination product development knowledge; strong analytical and communication skills.
Request for Proposal (RFP)
3w
Save
Mark Applied
Hide
Executive Director, Device Development
Chicago, Illinois, United States
$274k-$365k/yr OnsiteFull Time
18+ YOEMaster's in Biomedical or Mechanical Engineering and ~18 years pharmaceutical/biopharma device experience; 15+ years GMP experience; expertise in combination products, regulatory submissions, QMS, design controls, and program leadership.
SOLIDWORKS, CAD Software, Microsoft Word, Microsoft PowerPoint, Microsoft Outlook, Microsoft Excel
2mo
Save
Mark Applied
Hide
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.
2w
Save
Mark Applied
Hide
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)
1w
Save
Mark Applied
Hide
Senior Manufacturing Engineer
Cary, Illinois, United States
$86k-$143k/yr OnsiteFull Time
2+ YOEBachelor's degree in engineering or related technical field, 2+ years of manufacturing engineering experience, automated equipment troubleshooting, and process improvement experience. Medical device and validation experience preferred.
FMEA, SOP, GMP, IQ, OQ, PQ, FAT, VP, URS
1mo
Save
Mark Applied
Hide
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
1h
Save
Mark Applied
Hide
Manufacturing Engineer
Pittsboro or Carlsbad or Chicago or Durham or Greensboro or North Carolina
OnsiteFull Time
1+ YOEBachelor's degree in engineering or equivalent technical degree, 1+ year manufacturing experience, medical device regulations knowledge, process validation, PLC controls, CAD, Excel, and Word proficiency.
SolidWorks, 3D CAD, PLC, Microsoft Excel, Microsoft Word, LinkedIn Learning, IQ/OQ/PQ, PFMEA, DMR, CAPA
1mo
Save
Mark Applied
Hide
Senior Systems Engineer
Waukesha, Wisconsin, United States
HybridFull Time
8+ YOEBachelor's in STEM, minimum 8 years engineering experience with 6+ years systems engineering in regulated medical device environments; skills in requirements, V&V, risk management, FMEA, regulatory compliance, and technical leadership.
FMEA, IEC 60601, IEC 62304, ISO 14971, FDA, MDR
1mo
Save
Mark Applied
Hide
Project Engineer III
Rockford, Illinois, United States
$97k-$109k/yr OnsiteFull Time
10+ YOEBachelor's in engineering, 10+ years project engineering experience in regulated manufacturing/device industries, proficiency with Microsoft Project, AutoCAD, SAP, and Microsoft Excel, experience with design transfer, risk assessments (FMEA), and regulatory compliance (21 CFR 820, ISO standards).
Microsoft Project, AutoCAD, SAP, Microsoft Excel
1w
Save
Mark Applied
Hide
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
2mo
Save
Mark Applied
Hide
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
2mo
Save
Mark Applied
Hide
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
2mo
Save
Mark Applied
Hide
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
1mo
Save
Mark Applied
Hide
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%.
2mo
Save
Mark Applied
Hide
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
1w
Save
Mark Applied
Hide
Principal Product Usability Engineer
Libertyville, Illinois, United States
$142k-$204k/yr OnsiteFull Time
12+ YOEBachelor's degree and 12–15 years of related experience, with expertise in human factors, usability engineering, user-centered design, medical devices, research, analysis, mentoring, and cross-functional collaboration.
1d
Save
Mark Applied
Hide
Design Verification Engineer (Lab Project Specialist)
Chicago or United States or France or Germany or Brazil or Poland
$85k-$115k/yr OnsiteFull Time, Contract
3+ YOEBachelor's degree in engineering or related discipline, 3+ years in medical device development, verification, testing, or systems engineering, plus design controls, test methods, data analysis, and technical reporting experience.
Minitab, JMP, IEC 60601, ISO 11608, ISO 13485, ISO 14971, GR&R, PPE
2mo
Save
Mark Applied
Hide
Electrical Engineer, Power (31712)
Libertyville, Illinois, United States
$90k-$140k/yr OnsiteFull Time
5+ YOEBachelor's in Electrical Engineering required, PE preferred; 5+ years experience in power distribution design (arc flash, short circuit, load flow, protective device coordination); experience with cable, grounding, lighting, fire detection; travel 10-20%.
3mo
Save
Mark Applied
Hide
Engineering Associate Director (AD) - Device Assembly
Pleasant Prairie, Wisconsin, United States
$123k-$198k/yr OnsiteFull Time
7+ YOEBachelor's in engineering and 7+ years process engineering experience; leadership, equipment optimization, commissioning/qualification, regulatory knowledge, MES/Trackwise/ASRS experience; willing to travel and be on-call.
Manufacturing Execution Systems, electronic batch release, Automated Storage and Retrieval System (ASRS), Autonomous Guided Vehicles (AGVs), Trackwise, BMS
1mo
Save
Mark Applied
Hide
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
Explore Jobs