Medtronic
Healthcare
SeniorPrincipalSystemsEngineer
“Senior Principal Systems Engineer at Medtronic. Skills: Systems engineering, Product development, Requirements management. Support design and development. Apply systems engineering knowledge”
What You'll Achieve.
Successful completion of objectives
Industry & Context.
Critical thinking; Problem solving
What They're Looking For.
Must Have
System engineering requirements, Customer needs alignment, ET products integration, System verification and validation, System support and education, Product development leadership, Technical risk management, System definition, Customer needs identification, Written communication, Verbal communication, Judgment, Decision making, Critical thinking, Building relationships, Stakeholder alignment
Nice to Have
MedTech experience, Navigation and Imaging Systems experience, FDA (21CFR 820) familiarity, EU MDR Regulation familiarity, ISO 13485 familiarity, ISO 62304 familiarity, ISO 14971 familiarity
What You'll Do.
Support design and development
Apply systems engineering knowledge
Provide leadership for product development
Complete system engineering activities
Identify customer needs
Define system by translating needs
Define system architecture
Manage technical risks
Perform system verification
Perform system validation
Support system integration
Solve complex systems interaction problems
Work closely with cross-functional partners
Take product from ideation to market
Communicate product risk trade-offs
Lead cross-functional teams
Make timely decisions
Execute systems engineering activities
Plan systems engineering tasks
Monitor systems engineering tasks
Execute systems engineering tasks
Collaborate with stakeholders
Develop business needs
Develop customer needs
Design systems architecture
Align product development with needs
Contribute to defining new technologies
Support key design trade-offs
Provide alternate solutions
Create program risk profile
Create system integration strategy
Represent Systems Engineering organization
Provide input for regulatory submissions
Provide input for audits
Define interface requirements
Maintain requirements traceability
Manage interface changes
Manage system compatibility
How You'll Work.
Team & Collaboration
Cross-functional partners; Cross-functional teams; Internal and external stakeholders; Development teams; Research groups; Clinical groups; Regulatory groups; Product planning groups; Marketing groups; Stakeholders from other sites
Communication Scope
Written communication; Verbal communication; Oral communication
Process & Methodology
Product development life cycle, Program risk management
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