Principal Systems Engineer - Embedded(HYBRID - Open to Relocation)
Company: Stryker Corporation
Location: Fort Lauderdale
Posted on: October 16, 2024
Job Description:
Principal Systems Engineer - Embedded (HYBRID - Open to
Relocation)
Locations: Fort Lauderdale, Florida
Time Type: Full time
Posted on: Posted 7 Days Ago
Job Requisition ID: R527678
Work Flexibility: Hybrid or Onsite
Who We Want:
- 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.
- Curious learners: Engineers who seek out cutting-edge research
and information to expand and enhance their ability to develop
software.
- 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:
- 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.
- Able to architect an entire complex system, defining interfaces
and dependencies between components. Easily solves complex
system-level issues.
- Lead and mentor teams to solve significant and unique issues
where analysis of situations or data requires evaluation of
minimally defined problems.
- Work on the system aspects of a robotic system platform with
customers across the globe.
- Design, write and deploy robotic system hardware, software, and
firmware while meeting company quality expectations for
effectiveness, reliability, and safety.
- Design, write and deploy subsystem test platforms and
protocols.
- Interact with internal customers and marketing to draft/update
customer, system, and subsystem requirements.
- Coordinate with mechanical, electrical, software, and system
engineers to ensure that the system and subsystems designs meet
specified requirements.
- Analyze system and subsystems requirements to ensure they are
clear and verifiable, and that traceability of requirements is
accurately captured and documented.
- Incorporate post-market data into designs with targeted
precision.
- Collaborate in the development and execution of plans,
protocols, and reports for verification and validation
(V&V).
- Use common software tools, such as SolidWorks for CAD/CAM,
Minitab for statistical analysis, and MATLAB for analysis through
scripting.
- Apply FDA regulatory guidance, such as ISO 13485 / 14971 /
62304, to biomedical device development.
- Collaborate with Quality Assurance in analysis for the device
risk management file, including failure modes and effects analysis
(FMEA) and fault tree analysis (FTA).
- Collaborate with technical writers to create and revise
documentation.
Business Responsibilities:
- Possess an in-depth knowledge of the industry and competitive
landscape.
- Partner with customers and internal and external key opinion
leaders to develop technical strategies that meet clinical
needs.
- Strategize and execute customer-facing activities like the
voice of customer and customer-centric design across the
business.
- Collaborate on Financial/business modeling and support business
reviews to validate a technical approach.
- Lead cooperative efforts to ensure the design meets the needs
of all stakeholders.
- Lead and support team members to create or improve procedures,
policies, processes, systems, and technology requirements.
- Identify and implement design and process solutions and ensure
they are sustained over time.
- Hold team accountable to deliver high-quality results with
passion, energy, and drive to meet business priorities.
- Mentor, develop, and influence across the business,
intentionally building divisional relationships.
What You Need:
Minimum Qualifications (Required):
- Bachelor of Science in Software, Electrical, Mechanical,
Systems, or Biomedical Engineering & 8+ years of work
experience.
- Ability to communicate complex plans and technical information
to team members within and across businesses.
- Develop and utilize tools to enhance the company's
product/process development or performance.
- Experience with requirements management tools, such as JAMA,
Integrity, or DOORS.
- Experience managing product defects using tracking tools such
as Jira.
- Experience with embedded development using C, C++, Python
programming languages.
Preferred Qualifications (Strongly desired):
- Proficient in scripting and analysis using MATLAB.
- Proficient in statistical analysis with Minitab leveraging data
analysis to drive decision-making.
- Broad base of experience in implementing design methodologies
such as DFM, Reliability and Systems Design.
- 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.
- 3D CAD/CAM software, such as SolidWorks or Creo.
- EDA software, such as Altium.
- Experience with SysML and Model-based Systems
Engineering.
- Experience with SysML / MBSE software tools.
Med Device Compliance (Preferred):
- Divisional expert with extensive experience applying industry
standards for device development.
- Independent reviewer and advisor for the creation or refinement
of engineering documentation, such as the Design History
file.
- Lead the development of standards and regulations, working
closely with functions within and across business.
Travel Percentage: 10%
Stryker Corporation is an equal opportunity employer. Qualified
applicants will receive consideration for employment without regard
to race, ethnicity, color, religion, sex, gender identity, sexual
orientation, national origin, disability, or protected veteran
status. Stryker is an EO employer - M/F/Veteran/Disability.
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Keywords: Stryker Corporation, Oakland Park , Principal Systems Engineer - Embedded(HYBRID - Open to Relocation), Other , Fort Lauderdale, Florida
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