7 device engineer jobs at 7 companies in Maricopa, CA
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Staff Robotics Engineer
Goleta, California, United States
OnsiteFull Time
B. Braun: Develops and manufactures medical devices and pharmaceutical products globally.
14+ YOE14+ years robotics experience, BS in robotics/control/CS/CE, proficiency in robot kinematics, control systems, real-time software, C++ and Python, ROS/ROS2, medical-device safety and standards.
7+ YOEMS or PhD in Electrical Engineering, Applied Physics, or Materials Science; 7+ years in laser diode design; strong modeling and simulation; DOE experience; proficient in Python/MATLAB; device characterization
KARL STORZ: Developer and manufacturer of endoscopic medical equipment.
5+ YOEBachelor's in engineering or related field; 5+ years electro-mechanical design experience, 1–3 years PWB layout; proficiency with Altium Designer and SolidWorks; experience with SMT, PWB fabrication, test equipment, and medical device regulations.
Altium Designer, SolidWorks, CAD, oscilloscopes, DVMs, power supplies, signal generators, GD&T, ASME Y14.5, FDA 21 CFR Part 820, ISO 13485, ISO 9001
HRL Laboratories: Conducts advanced scientific research for aerospace and automotive industries.
1+ YOEB.S. or M.S. in electrical engineering; 1+ year testing/integration of power, control, or analog electronics; experience with SiC/GaN devices; V>1kV a plus; PCB layout and SPICE a plus; Matlab/Python/LabVIEW etc.; must lift 50 lbs and travel.
Teladoc HealthNYSE: TDOC: Provides on-demand virtual medical care and mental health services.
7+ YOEBachelor's degree in engineering, quality, regulatory affairs or life sciences; 7+ years in medical device or regulated industry; ISO 13485, CAPA, audits, supplier quality, risk management, and design control experience.
Agilent TechnologiesNew York Stock Exchange: A: Providing instruments, software, and consumables for laboratory scientific discovery.
8+ YOE8+ years regulatory affairs in IVDs or medical devices; digital pathology or software-based diagnostics experience; bachelor’s in science or engineering; knowledge of SaMD and AI/ML regulatory frameworks; experience with FDA and EU IVDR/MDR.