Principal Systems Engineer - Embedded(HYBRID - Open to Relocation)
Date de publication :
03 septembre 2024Taux d'activité :
100%Type de contrat :
Durée indéterminée- Lieu de travail :Fort Lauderdale
Who We Want:
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Dedicated achievers. Relentless about quality, people who thrive in a fast-paced environment and will stop at nothing to ensure a project is complete and meets regulations and expectations.
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Curious learners. Engineers who seek out cutting-edge research and information to expand and enhance their ability to develop software.
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Motivated product launchers. Engineers who bring strategic direction and drive for execution to ensure products are developed and launched with precision.
What you will do
Technical Competencies:
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Lead technical team members in the design, development, modification, and evaluation of design modules, sub-systems, or assemblies.
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Translate user needs to design inputs/ specifications and produce architectural-level layouts and platform designs.
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Able to architect an entire complex system, defining interfaces and dependencies between components. Easily solves complex system-level issues.
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Lead and mentor teams to solve significant and unique issues where analysis of situations or data requires evaluation of minimally defined problems.
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Work on the system aspects of a robotic system platform with customers across the globe.
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Design, write and deploy robotic system hardware, software, and firmware while meeting company quality expectations for effectiveness, reliability, and safety.
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Design, write and deploy subsystem test platforms and protocols.
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Interact with internal customers and marketing to draft/update customer, system, and subsystem requirements.
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Coordinate with mechanical, electrical, software, and system engineers to ensure that the system and subsystems designs meet specified requirements.
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Analyze system and subsystems requirements to ensure they are clear and verifiable, and that traceability of requirements is accurately captured and documented.
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Incorporate post-market data into designs with targeted precision.
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Collaborate in the development and execution of plans, protocols, and reports for verification and validation (V&V).
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Use common software tools, such as SolidWorks for CAD/CAM, Minitab for statistical analysis, and MATLAB for analysis through scripting.
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Apply FDA regulatory guidance, such as ISO 13485 / 14971 / 62304, to biomedical device development.
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Collaborate with Quality Assurance in analysis for the device risk management file, including failure modes and effects analysis (FMEA) and fault tree analysis (FTA).
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Collaborate with technical writers to create and revise documentation.
Business Responsibilities:
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Possess an in-depth knowledge of the industry and competitive landscape
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Partner with customers, internal and external key opinion leaders to develop technical strategies that meet clinical needs
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Strategize and execute customer-facing activities like the voice of customer and customer-centric design across the business
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Collaborate on Financial /business modeling and support business reviews to validate a technical approach
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Lead cooperative efforts to ensure the design meets the needs of all stakeholders
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Lead and support team members to create or improve procedures, policies, processes, systems, and technology requirements
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Identify and implement design and process solutions and ensures they are sustained over time
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Hold team accountable to deliver high quality results with passion, energy, and drive to meet business priorities
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Mentor, develop and influence across the business, intentionally building divisional relationships
What You Need
Minimum Qualifications (Required)
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Bachelor of Science in Software, Electrical, Mechanical, Systems, or Biomedical Engineering & 8+ years of work experience
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Ability to communicate complex plans and technical information to team members within and across businesses
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Develop and utilize tools to enhance the company’s product/process development or performance
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Requirements management tools, such as JAMA, Integrity, or DOORS.
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Experience managing product defects using tracking tools such as Jira.
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Experience with embedded development using C, C++, Python programming languages.
Preferred Qualifications (Strongly desired):
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Proficient in scripting and analysis using MATLAB.
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Proficient in statistical analysis with Minitab leveraging data analysis to drive decision-making
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Broad base of experience in implementing design methodologies such as DFM, Reliability and Systems Design
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High degree of experience in medical device design (or designing in a highly regulated industry) and ability to utilize Requirements Management Tools and System Modeling Tools
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3D CAD/CAM software, such as SolidWorks or Creo, etc.
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EDA software, such as Altium.
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Experience with SysML and Model-based Systems Engineering
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Experience with SysML / MBSE software tools
Med Device Compliance (Preferred)
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Divisional expert with extensive experience applying industry standards for device development
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Independent reviewer and advisor for the creation or refinement of engineering documentation, such as the Design History file
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Lead the development of standards and regulations, working closely with functions within and across business