59 medical device engineer jobs at 31 companies in Valhalla, NY
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Senior Medical Device Research and Development Engineer
Brooklyn, New York, United States
$100k-$160k/yr OnsiteFull Time
5+ YOEBS in engineering or related field required, 5+ years product development experience (4+ in cGMP R&D), hands-on medical device R&D, FDA/ISO knowledge, SolidWorks and Microsoft Office proficiency, strong leadership and experiment design skills.
SolidWorks, Microsoft Excel, Microsoft Word, Microsoft PowerPoint
1mo
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GRA Device Associate - Medical Devices and Combination Products (Senior Manager)
Morristown or Cambridge or Framingham
$122k-$177k/yr HybridFull Time
6+ YOEBachelor's in science/engineering required (advanced degree preferred); 6+ years industry experience, 3+ years regulatory experience; experience with regulatory filings and health authority interactions; strong communication and leadership skills.
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Principal Systems Engineer - Medical Devices
Parsippany, New Jersey, United States
$132k-$165k/yr HybridFull Time
15+ YOE7+ MgmtAdvanced engineering degree and 15+ years developing electronic hardware and embedded software for real-time medical instruments; 10+ years systems engineering; 7+ years leading systems engineering; knowledge of FDA/EC regulations and human factors.
real time operating systems, digital signal processing
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Electrical Engineer
Hawthorne, New York, United States
$95k-$135k/yr OnsiteFull Time
3+ YOEBachelor's in electrical engineering, 3+ years product development experience, circuit and PCB design, embedded hardware and test equipment proficiency, troubleshooting, and medical device/regulatory familiarity.
oscilloscopes, multimeters, logic analyzers, power supplies, PCB design tools, schematic capture tools
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Sr. Biomedical Engineer
Tarrytown, New York, United States
$120k-$140k/yr HybridFull Time
5+ YOEMS or PhD in biomedical/mechanical engineering or related field; 8+ years post-MS or 5+ years post-PhD industry experience in medical device R&D; expertise in biomechanics, human factors, CFD/FEA, and validation for Class I/II devices.
ANSYS, COMSOL, SolidWorks Simulation, CFD, FEA
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Staff Engineer
Allendale or Leesburg
$128k-$136k/yr OnsiteFull Time
4+ YOEBachelors in Mechanical/Biomedical Engineering required (Master's preferred), 4+ years medical device product development experience, proficiency with parametric CAD (Creo or SolidWorks), GD&T, experience with design controls and regulated industry standards (FDA, ISO 13485).
Creo, SolidWorks, GD&T
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Principal Mechanical Engineer - Instruments
Orange or Sunnyvale
$220k-$330k/yr OnsiteFull Time
15+ YOEBachelor’s or Master’s in Engineering; 15+ years medical device exp; advanced mechanical instrument development; regulatory compliance; design leadership and mentorship.
Mechanical Engineering, Robotics, Medical Devices, Regulatory Compliance
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Mechanical Design Engineer
Madison, New Jersey, United States
HybridFull Time
2+ YOEBachelor's in Mechanical Engineering, 2+ years mechanical design experience, proficiency in CAD (SolidWorks preferred), experience with design verification/testing, and ability to work in regulated medical device environments.
CAD, SolidWorks
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Senior Product Engineer- Mechanical
Trumbull, Connecticut, United States
OnsiteFull Time
5+ YOEExpertise in SolidWorks and GD&T, medical device development with design control, DFM/DFSS, FEA/CFD preferred, statistical methods, hands-on prototyping, and demonstrated experience delivering medical device products (BS+5yrs or MS+3yrs).
SolidWorks, GD&T, Design for Manufacturing (DFM), Design for Six Sigma (DFSS), FEA, CFD
6d
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Senior Mechanical Engineer (Contract)
Olathe or Lyndhurst
OnsiteFull Time, Contract
10+ YOEBachelor's in mechanical engineering and 10+ years designing, developing, and testing mechanical systems; CAD, SolidWorks PDM, GD&T, FEA, prototyping, medical-device safety, and manufacturing experience required or preferred.
Computer-Aided Design (CAD), SolidWorks PDM, 3D printing, Finite Element Analysis (FEA), Computational Fluid Dynamics (CFD), IEC 60601-1, ISO 10993-1, UL, CE, FDA
4w
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Senior Mechanical Engineer
Lyndhurst or Olathe
$116k-$139k/yr OnsiteFull Time
10+ YOEBachelor's in Mechanical Engineering required, 10+ years industry experience designing, prototyping and testing mechanical systems for medical devices; SolidWorks/PDM experience, GD&T, FEA/FEM, IEC 60601-1 familiarity, regulatory documentation and leadership experience.
SolidWorks, SolidWorks PDM, FEA, FEM, CFD
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Sr. Engineer, Process Development - Wayne, NJ
Wayne, New Jersey, United States
$115k-$135k/yr HybridFull Time
5+ YOEMaster's preferred or bachelor's in mechanical/biomedical engineering with 5+ years process development/design transfer in medical device industry; Six Sigma belt, validation and statistical analysis experience, SolidWorks/Creo proficiency.
SolidWorks, Creo, DOE, SPC, GD&T, FMEA, IQ/OQ/PQ
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Sr. Staff Engineer - Process & Equipment Design
Franklin Lakes, New Jersey, United States
$169k-$270k/yr OnsiteFull Time
10+ YOEBachelor's degree in engineering and 10 years of engineering and process development experience in regulated manufacturing; medical device experience, capital project leadership, validation, FMEA, Lean, and SPC knowledge required.
FMEA, Lean, SPC, FDA, ISO, GMP
3w
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Sr. New Product Development (NPD) Engineer
Rockaway, New Jersey, United States
OnsiteFull Time
10+ YOEBachelor's in engineering plus 10+ years in Class II medical device development; hands-on PCB and embedded software experience; verification protocol and regulatory knowledge (IEC 60601-1, IEC 62304, IEC 62366, ISO 14971).
PCB, oscilloscope, logic analyzer
1w
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Field Service Engineer- Long Island New York
New York or New York City or New York
$45-$58/hr FieldFull Time
2+ YOEAssociate's degree or equivalent experience, 2 years of relevant experience, English fluency, advanced technical and analytical skills, medical device experience preferred, and ability to lift 50 pounds.
ServiceMax, CRM, lasers
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Quality Engineer III
Bethel, Connecticut, United States
$65k-$102k/yr OnsiteFull Time
2+ YOE2+ years quality engineering experience in medical device manufacturing, familiarity with ISO 13485 and FDA 21 CFR 820, technical writing, Minitab/statistical tools, BS in Engineering, auditing/supplier qualification experience.
Minitab
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Clinical Engineer
New Haven, Connecticut, United States
OnsiteFull Time
Bachelor's in biomedical engineering or related field required; experience with clinical information/patient monitoring systems, medical device interoperability, project implementation/support, customer requirements gathering, and willingness to be on-call and travel to system sites.
telemetry/physiological monitors, patient monitoring systems, server technology, wifi, monitoring networks
1w
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Staff Design Quality Engineer
Burlington or California or New York City
$145k-$160k/yr HybridFull Time
Experience in medical device quality engineering, design controls, risk management (ISO 14971), human factors, cybersecurity, AI/ML-enabled device considerations, and cross-functional leadership; bachelor\u0002s degree required.
eQMS, PLM
3mo
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Senior Supplier Quality Engineer
Warren, New Jersey, United States
$125k-$150k/yr HybridFull Time
5+ YOEBachelor's in engineering/life sciences, formal auditor training (ISO 13485/GMP), 5+ years supplier quality/quality engineering in medical device or pharma, experience leading supplier audits, CAPA, QTAs, knowledge of FDA and EU GMP regs, eQMS experience.
eQMS, Veeva, ENNOV
2mo
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Senior Quality Engineer/Analyst
New York, New York, United States
$120k-$160k/yr HybridFull Time
5+ YOE5+ years in a medical device quality/regulatory role; strong multi-project management; knowledge of ISO 13485, 21 CFR 820, IEC 62304, ISO 14971; cross-functional collaboration; detail-oriented.
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