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Stryker - Fort Lauderdale, FL
posted 2 months ago
About the position
The Principal Systems Engineer - Embedded is responsible for leading technical teams in the design, development, and evaluation of complex systems, particularly in the biomedical device sector. This role requires a deep understanding of system architecture, regulatory compliance, and collaboration across various engineering disciplines to ensure product quality and effectiveness. The engineer will also engage with customers to align technical strategies with clinical needs and mentor team members to foster a culture of high-quality results and continuous improvement.
Responsibilities
- Lead technical team members in the design, development, modification, and evaluation of design modules, sub-systems, or assemblies.
- Translate user needs to design inputs/specifications and produce architectural-level layouts and platform designs.
- Architect complex systems, defining interfaces and dependencies between components, and solve complex system-level issues.
- Mentor teams to address significant and unique issues requiring evaluation of minimally defined problems.
- Work on system aspects of robotic platforms with global customers.
- Design, write, and deploy robotic system hardware, software, and firmware while meeting quality expectations.
- Design, write, and deploy subsystem test platforms and protocols.
- Interact with internal customers and marketing to draft/update requirements.
- Coordinate with mechanical, electrical, software, and system engineers to ensure design compliance with requirements.
- Analyze system and subsystems requirements for clarity and verifiability, ensuring traceability is documented.
- Incorporate post-market data into designs with precision.
- Collaborate in the development and execution of verification and validation plans, protocols, and reports.
- Utilize software tools like SolidWorks, Minitab, and MATLAB for design and analysis.
- Apply FDA regulatory guidance to biomedical device development.
- Collaborate with Quality Assurance on device risk management and analysis.
- Work with technical writers to create and revise documentation.
Requirements
- Bachelor of Science in Software, Electrical, Mechanical, Systems, or Biomedical Engineering.
- 8+ years of work experience in relevant fields.
- Ability to communicate complex plans and technical information effectively.
- Experience with requirements management tools such as JAMA, Integrity, or DOORS.
- Experience managing product defects using tracking tools like Jira.
- Proficiency in embedded development using C, C++, and Python programming languages.
Nice-to-haves
- Proficient in scripting and analysis using MATLAB.
- Proficient in statistical analysis with Minitab.
- Experience in implementing design methodologies such as DFM, Reliability, and Systems Design.
- Experience in medical device design or in a highly regulated industry.
- Experience with 3D CAD/CAM software like SolidWorks or Creo.
- Experience with EDA software such as Altium.
- Experience with SysML and Model-based Systems Engineering.
Benefits
- Work flexibility (Hybrid or Onsite)
- Equal opportunity employer
- Diversity and inclusion initiatives
