188 medical device engineer jobs at 75 companies in Epping, NH
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Device Engineering Sr. Engineer
Cambridge, Massachusetts, United States
$115k-$156k/yrHybridFull Time
AmgenNASDAQ: AMGN: Develops and manufactures biotechnology medicines for serious diseases.
Doctorate/Master with 2+ yrs or Bachelor with 4+ yrs in engineering; experience in medical devices; design for robustness; cross-disciplinary work; English fluency.
Injection Molding, DFR Tools, Quality Management Systems
Magnendo: Develops robotic magnetic navigation technology for endovascular interventions.
2+ YOE2+ years production software engineering; experience in robotics, computer vision/ML, or systems/infrastructure; comfortable with Python,C++,Linux,GIT; ability to work in high-reliability regulated environments.
Kailera Therapeutics: Developing clinical-stage injectable and oral therapies for obesity.
10+ YOE3+ Mgmt10+ years medical device or combination product development experience with 3+ years leadership; expertise in autoinjectors/prefilled syringes/multidose pens, design controls, risk management, verification/validation, human factors, and regulatory submissions.
Johnson & JohnsonNYSE: JNJ: Provides pharmaceutical products and medical technology healthcare solutions.
10+ YOE10+ years information security experience, 8+ years in embedded/IoT or medical device security; bachelor’s or equivalent; strong threat modeling, risk assessment (CVSS 3.1/STRIDE), regulatory knowledge (FDA, NIST, IEC), and secure architecture skills.
QNX QOS, Yocto, Linux Ubuntu, Alpine, AWS, Azure, OWASP, mTLS, HSMs, TPM, PKI, SBOM, STRIDE, CVSS 3.1, FIPS 140-3, IEC 62443, NIST 800-53, Bluetooth LE, NFC, Wi-Fi, 5G
BiogenNASDAQ: BIIB: Develops therapies for neurological and neurodegenerative diseases.
7+ YOEBS in engineering or related discipline, 7+ years in medical device/combination product quality with design control and risk management expertise, regulatory knowledge, and cross-functional leadership experience.
Device Quality Engineer - Device Risk Management and Surveillance Excellence
Cambridge, Massachusetts, United States
$90k-$130k/yrOnsiteFull Time
SanofiEuronext Paris: SAN: Researches, develops, and manufactures medicines and vaccines globally.
5+ YOEBS in Engineering or related science; MS desired; 5+ years medical device experience; 3+ years risk management and post-market surveillance; ISO 14971, MDR, and 21 CFR 820 knowledge; English required; French or German a plus.
Senior Medical Device Software Engineer (Python / C++)
Boston or United States
HybridFull Time
Intellias: Global software engineering and digital transformation services provider.
4+ YOEBachelor’s degree in CS/CE/EE (or higher) with relevant experience; deep Python and C++ expertise, embedded/real-time software, ROS, Linux, Bluetooth, CI/CD and Git experience; strong communication and problem-solving.
C++, Python, ROS, Linux, Git, CI/CD, AWS, Azure, Bluetooth
Senior Quality Systems Engineer- CAPA/Complaints Support - Medical Device #8161
Boston, Massachusetts, United States
OnsiteContract, Full Time
ECI: Provides regulatory and engineering consulting for life sciences companies.
5+ YOE5+ years medical device experience, Bachelor’s in biomedical/mechanical/electrical engineering required, experience executing CAPA, regulatory knowledge for Class II/III devices, strong analytical and problem-solving skills.
TakedaTokyo Stock Exchange / New York Stock Exchange: 4502 / TAK: Researches, develops, and manufactures prescription pharmaceutical medicines.
7+ YOEBachelor's in engineering or related field,7+ years QA/engineering experience in medical devices/combination products,knowledge of ISO 13485,ISO 14971,MDR,MDSAP,21 CFR Part 820,experience with regulatory submissions and risk management.
Analog DevicesNASDAQ: ADI: Designs and manufactures semiconductors for signal processing and power management.
7+ YOE7+ years cybersecurity/product security experience supporting FDA-regulated medical devices or SaMD, Master's degree (Ph.D preferred), threat modeling, vulnerability management, and familiarity with FDA guidance and cybersecurity frameworks.
Freudenberg Group: Global manufacturer of specialized technical components and advanced materials
8+ YOEBachelor's in engineering/chemistry/biology, 8+ years in medical device, 6+ years program/project management in manufacturing, knowledge of ISO/GMP/regulatory (FDA/MDR/Health Canada/PMDA), DOE/Lean/Six Sigma experience.
Senior Electrical Engineer – Medical Imaging (Bedford, MA)
Bedford, Massachusetts, United States
OnsiteFull Time
PhilipsEuronext Amsterdam: PHIA: Manufactures medical imaging systems and personal care appliances.
5+ YOE5+ years in electrical engineering; medical devices or regulated industries preferred; PCB design (Altium); analog/digital circuits; IEC 60601-1, EMC; Bachelor's or Master's in Electrical Engineering.
AbbottNYSE: ABT: Manufactures medical devices, diagnostics, and nutritional health products.
5+ YOEBachelor's in Electrical or Biomedical Engineering,5+ years engineering experience in design/testing/manufacturing,experience with electro-mechanical designs,RF antenna work,automation and data analysis,knowledge of FDA/ISO quality and regulatory requirements.
Mass General Brigham: Provides integrated medical care, research, and clinical training services.
0+ YOEBachelor's degree in a related field; preferred device or medical engineering experience; project management, interdisciplinary teamwork, technical troubleshooting, writing, fabrication, and engineering tool skills.
PCI Pharma Services: Integrated pharmaceutical development, manufacturing, and global packaging services.
5+ YOEBachelor's degree in engineering and 5+ years of engineering, facilities, clean utilities, or plant utilities experience, preferably in biotechnology, medical device, or pharmaceutical manufacturing.
Computerized Maintenance systems (CMMS), AutoCAD, SolidWorks, PLC, SCADA, Microsoft Word, Microsoft Excel, Microsoft Project, Microsoft PowerPoint
Verily: Developing data-driven technologies for clinical research and precision health.
5+ YOE5+ years software quality engineering in regulated medical device/SaMD, medical device cybersecurity expertise, knowledge of IEC/ISO standards, experience with risk management and secure SDLC, proficiency with Jira/GitHub/Google Workspace.
Google Workspace, Jira, GitHub, Gemini, Claude, ChatGPT
Instylla: Develops resorbable embolic agents for interventional oncology
2+ YOEBachelor's degree in engineering or materials science, 2+ years in medical device engineering, process validation, manufacturing methods, GMP/GDP, statistical analysis, and technical documentation.
QAD, Oracle, SAP, Microsoft Office, Microsoft Excel, SolidWorks, 3D CAD, Enterprise Resource Planning (ERP), Gage R&R, IQ/OQ/PQ, DOE, 21 CFR Part 820, EU MDR
Terrestrial: Develops micro-array patch technology for patient-friendly drug delivery.
6+ YOEBachelor's in engineering, 6+ years manufacturing engineering in pharma/biotech/medical device, cGMP knowledge, IQ/OQ/PQ experience, MES/EBR support, isolator/aseptic experience, lead cross-functional projects and mentor engineers.
Manufacturing Execution System (MES), Electronic Batch Records (EBR)