Johnson & Johnson MedTech is seeking a Senior Systems Engineer to lead the design and integration of medical devices in Santa Clara, California. The role requires a strong background in engineering, with responsibilities including cross-functional collaboration and system development for surgical technologies
Job Summary
The Senior Systems Engineer is responsible for the system level design and integration of capital equipment products that consist of electrical and electro-mechanical subsystems.
You will lead multi-functional teams to design and develop groundbreaking medical devices!
This is an excellent opportunity for you to have a key role bringing exciting new products to market while also providing the opportunity for professional growth!
Matching Summary
Match Score: 85
Johnson & Johnson MedTech is seeking a Senior Systems Engineer to lead the design and integration of medical devices in Santa Clara, California. The role requires a strong background in engineering, with responsibilities including cross-functional collaboration and system development for surgical technologies.
Salary
Base: $125,000.00 - $201,250.00; Bonus/Equity: Not specified; Benefits: Vacation, Sick time, Holiday pay, Work/Personal/Family Time, Parental Leave, Bereavement Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off
Skills & Requirements
Must-have
system level design and integration
electrical and electro-mechanical subsystems
cross-functional teams
system requirements
use cases, trade studies, and risk assessments
Python, C++, or MATLAB proficiency
Nice-to-have
revolutionizing the world of medical robotics
passion for improving and expanding surgery
flexible, self-motivated, curious
Key Requirements
BS/BA Degree in Biomedical, Electrical, Computer Science, Mechanical or any related engineering field
4+ years' experience with BS/BA or 3+ years' experience with advanced degree
Strong proficiencies with at least one engineering field
Good understanding of system lifecycle phases and design control processes
Knowledge of FDA and ISO regulations
Experience writing requirements for complex electromechanical systems
Ability to travel up to 10%
FDA CFR Part 820 and/or ISO 13485 knowledge preferred
Experience working with DFMEAs or other risk analysis tools highly preferred