You will lead system-level design for complex implantable medical devices. You own the transition from user needs to verified architecture.
Responsibilities
Develop system requirements from user needs and stakeholder inputs.
Design and document system architecture, guiding hardware, firmware, and software implementation.
Resolve complex system interaction problems using critical analysis.
Create design documentation including requirements rationale, tracing, and system change analysis.
Write technical reports to satisfy external regulatory agency requirements.
Required Skills
Bachelor’s degree with 5+ years of experience, or Master’s with 3+ years, in Electrical Engineering, Computer Engineering, Computer Science, or a related field.
Experience in the design, development, and testing of embedded systems or active implantable medical devices.
Proficiency in Python, C/C++, or Java.
Ability to interpret and develop system requirements and specifications.
Hands-on experience with electronic bench test equipment including oscilloscopes, DMMs, and Data Acquisition devices.
Experience using version control, defect tracking, and peer review tools (Accurev, JIRA, Windchill).
Preferred Skills
Experience with system development lifecycle processes and Class II/III medical device regulations.
Familiarity with requirements management/PLM tools and Agile methodologies.
Background in product concept development and verification/validation of engineering requirements.