Systems Engineer II - Medical Devices (EP)

Abbott; Saint Paul (MN); On-site; USD 61,000 - 123,000; Full time

Job summary

Abbott in Saint Paul, MN is seeking a Systems Engineer II to translate clinical needs into system requirements and develop architectures for electrophysiology products. You will work across abstraction levels from concepts to implementation with cross-functional teams in a medical devices environment.

The role emphasizes verification/validation planning, system characterization, and risk management. A strong foundation in engineering and collaboration with Marketing, Regulatory, and QA teams is

Qualifications

• 2+ years of experience in an R&D or medical device environment.
• B.S. in Electrical, Biomedical, or Systems Engineering or related discipline.

Responsibilities

• Analyze and translate stakeholder and clinical needs into system requirements.
• Develop, review, and maintain system architecture across structural, behavioral, and dependability views.
• Decompose system requirements and allocate functions to system elements.
• Lead or support system verification and validation planning and execution.
• Collaborate with Marketing, Product R&D, Preclinical, Design Assurance, Regulatory, and Verification teams.
• Define and execute system characterization, integration, and performance evaluation activities.
• Interface with end users to align design with clinical workflows.
• Apply multidisciplinary engineering judgment to design, develop, integrate, and troubleshoot complex electrophysiology systems.
• Contribute to risk management, interface management, and configuration control.

Skills

Systems engineering

Python

MATLAB

Statistical analysis

Education

B.S. in Electrical Engineering

B.S. in Biomedical Engineering

M.S. in Electrical Engineering

Tools

Python

MATLAB

Minitab

JMP

Job description

Abbott in Saint Paul, MN is seeking a Systems Engineer II to translate clinical needs into system requirements and develop architectures for electrophysiology products. You will work across abstraction levels from concepts to implementation with cross-functional teams in a medical devices environment.

The role emphasizes verification/validation planning, system characterization, and risk management. A strong foundation in engineering and collaboration with Marketing, Regulatory, and QA teams is