Systems Engineer II: Electrophysiology Devices

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

Job summary

Abbott in Plymouth, MN is seeking a Systems Engineer II in the Electrophysiology Systems Engineering team focused on Left Atrial Appendage Occlusion. You will help develop catheter-based devices and architecture across the product lifecycle, collaborating with Marketing, R&D, Regulatory and Verification to meet patient needs.

The role requires a BS in a related engineering field and 2+ years in medical device R&D, with strong problem-solving, communication, and teamwork skills.

Qualifications

• BS degree in a engineering discipline (Systems/Biomedical/Mechanical) or related.
• 2+ years in an R&D or medical device environment or equivalent systems engineering experience.
• Strong technical knowledge with ability to think critically, problem solve, and communicate clearly in spoken and written form.

Responsibilities

• Develop and maintain system architecture including structural, behavioral, and dependability views.
• Translate stakeholder and clinical needs into system requirements.
• Lead or support verification and validation planning and execution.
• Collaborate with Marketing, Product R&D, Preclinical, Design Assurance, Regulatory, and Verification teams.
• Define system characterization, integration, and performance evaluation activities.
• Interface with end users to align design with clinical workflows.
• Contribute to risk management and configuration control in new product development programs.
• Write and submit intellectual property (patents).

Skills

Cross functional collaboration

Critical thinking

Problem solving

Clear communication

Education

B.S. in Systems Engineering

B.S. in Biomedical Engineering

B.S. in Mechanical Engineering

Tools

SolidWorks

Minitab

JMP

Job description

Abbott in Plymouth, MN is seeking a Systems Engineer II in the Electrophysiology Systems Engineering team focused on Left Atrial Appendage Occlusion. You will help develop catheter-based devices and architecture across the product lifecycle, collaborating with Marketing, R&D, Regulatory and Verification to meet patient needs.

The role requires a BS in a related engineering field and 2+ years in medical device R&D, with strong problem-solving, communication, and teamwork skills.