16 medical device engineer jobs at 11 companies in Slinger, WI
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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
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Sr. Principal Systems Engineer
Milwaukee, Wisconsin, United States
$128k-$176k/yr HybridFull Time
8+ YOEBachelor's in engineering, 8+ years medical device engineering experience, knowledge of ISO 14971 and IEC 60601, systems engineering in Agile SAFe, risk management, DHF ownership, and experience with MATLAB, Azure DevOps, Polarion, Trackwise.
MATLAB, Azure DevOps, Polarion, Trackwise
2w
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Test Engineer II
Wauwatosa or Milwaukee
OnsiteFull Time
3+ YOEBachelor's degree in mechanical, biomedical, or related engineering; 3–5 years testing or designing products; medical device certification, electromechanical systems, CAD, analysis, and project collaboration experience.
MPLAB, SolidWorks, Jira, Monday, Todoist, FEA, CNC, PCB, PCBA
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Product Quality Engineer
Pewaukee, Wisconsin, United States
$79k-$111k/yr OnsiteFull Time
3+ YOEBachelor\u0002s in engineering or equivalent, 3+ years quality/regulatory experience (medical device preferred), proficiency with MS Office, ERP, eQMS, CAD, strong data analysis and auditing skills.
Microsoft Outlook, Microsoft Word, Microsoft Excel, ERP, eQMS, CAD
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Senior Quality Manufacturing Engineer - Hartland, WI
Hartland, Wisconsin, United States
$101k-$152k/yr OnsiteFull Time
4+ YOEBachelor's in engineering or related field, 4+ years quality/engineering experience, knowledge of medical device regulations (21 CFR, ISO13485, MDD/MDR), SPC and CAPA experience, advanced Excel and MS Office skills.
Microsoft Office Suite, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook, SPC
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Manufacturing Engineer Assembly
Milwaukee, Wisconsin, United States
OnsiteFull Time
2+ YOEDesign and optimize assembly processes for electromechanical medical devices; 2+ years manufacturing experience; proficiency with CAD (SolidWorks/ProE/AutoCAD), ERP, GMP, PFMEA, IQ/OQ/PQ, and problem-solving methodologies.
ERP, SolidWorks, ProE, AutoCAD, Microsoft Office Suite
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Manufacturing Engineer Fabrication
Sturtevant, Wisconsin, United States
OnsiteFull Time
2+ YOEDesign and optimize metal fabrication processes for medical device assemblies; 2+ years fabrication experience; proficiency with CAD (SolidWorks/ProE/AutoCAD), PFMEA, GMP, ISO 9001/13485, validation (IQ/OQ/PQ), and continuous improvement methods.
SolidWorks, ProE, AutoCAD, 4i Blank and Form Programming Software, Influent, SigmaNest, Microsoft Office
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Quality Engineer I
Sturtevant, Wisconsin, United States
$78k-$94k/yr OnsiteFull Time
1+ YOEBachelor's degree in engineering, 1+ years of relevant experience, Microsoft Office proficiency, fluent English, ISO 13485 and 21 CFR 820 knowledge, and medical device manufacturing experience.
Microsoft Office, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Access, ISO 13485, 21 CFR 820, SPC, FMECA, DOE, IQ, OQ, CAPA, NCR, SCAR
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Quality Engineer Associate I
Franksville or Racine
OnsiteFull Time
Bachelor's degree or equivalent experience required. Preferred engineering or physical science degree, GLP/GMP and medical device experience, regulatory knowledge, quality systems expertise, laboratory skills, and LIMS or quality management software experience.
Nonconformance Records (NCR), Corrective and Preventive Action (CAPA), Change Control, Design History File (DHF), pFMEA, Laboratory Information Management Systems (LIMS), FDA, USP, EP, BP, ICH
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Quality Engineer - Systems Assurance
Waukesha, Wisconsin, United States
OnsiteFull Time
7+ YOE7+ years medical device/biotech experience with CAPA and complaint handling; strong knowledge of FDA 21 CFR 820, ISO 13485, EU IVDR; RCA, risk management, eQMS experience; leadership and communication skills.
eQMS, TrackWise, MasterControl, SAP
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Field Service Engineer II
Milwaukee or Chicago
FieldFull Time
5+ YOEInstall, maintain, troubleshoot, and repair Cytovale Systems; 5+ years medical device field or customer support experience; ability to lift 50 lbs; valid driver’s license; comply with vendor vaccination requirements.
6d
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Electronic Technician II
Pewaukee, Wisconsin, United States
$26-$31/hr OnsiteFull Time
1+ YOEHigh school diploma or equivalent, 1–3 years of electro-mechanical manufacturing experience, and ability to interpret technical instructions. Medical device experience preferred.
Microsoft Outlook, Microsoft Excel, Microsoft Word, ERP, eQMS, CAD
3w
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Design Quality Assurance Manager
Wauwatosa, Wisconsin, United States
HybridFull Time
5+ YOE3+ MgmtLead quality oversight for medical device design controls, risk management, and regulatory compliance (FDA QSR, ISO 13485, MDSAP, ISO 14971); supervise design quality engineers; 5+ years medical device QA experience.
FDA QSR, ISO 13485, MDSAP, ISO 14971, IEC 60601, IEC 62366, IEC 62304, EU MDR
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Senior Program Manager - Ultrasound Probes
State College or Zipf or Niskayuna or Oslo or Paris or Munich or Waukesha or Jenbach or Valbonne or United States
$180k-$270k/yr OnsiteFull Time
6+ YOEBachelor's degree in engineering/related field, significant program management experience in medical device or regulated industry, ability to lead complex cross-functional global programs, strong communication and governance skills.
2mo
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Regional Leadless Specialist, Cardiac Rhythm Management - Milwaukee, WI/Minneapolis, MN
Milwaukee or Minneapolis or United States
$68k-$136k/yr FieldFull Time
3+ YOEBachelor's in engineering or related field (or equivalent experience), 3+ years clinical medical device experience (CRM preferred), strong communication and presentation skills, comfort in hospital settings, Microsoft Office proficiency, substantial business travel (~50%).
Microsoft Office
3w
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Design Quality Assurance Manager
Milwaukee or Wauwatosa
HybridFull Time
5+ YOE3+ MgmtBachelor's in engineering required, advanced degree preferred. 5–10 years medical device quality experience, 3+ years senior design quality supervisory experience, CAPA ownership, design controls and risk management expertise, knowledge of FDA QSR/ISO/MDSAP.
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