Senior Neuromodulation Systems Engineer - Implantable Devices

Abbott (abbottcareers2 board); United States; On-site; USD 120,000 - 160,000; Full time

Benefits offered by this job

Health coverage

Tuition reimbursement

Retirement plan

Job summary

Abbott in Plano, TX is seeking a Senior Systems Engineer for Neuromodulation. You will develop and maintain architectures for implantable neuromodulation systems, translate clinical and business needs into measurable system requirements, and collaborate with cross-functional teams to drive design tradeoffs and integration.

The role emphasizes risk management, verification/validation, and regulatory documentation in a regulated development environment, with opportunities for impact across patient

Qualifications

• Bachelor's degree in a related engineering or scientific field.
• 6+ years of R&D or product development in complex multidisciplinary products.
• Experience defining architectures, requirements, and interfaces.
• Understanding hardware, firmware, software, mechanics, and UX interactions.

Responsibilities

• Develop and maintain architectures, system requirements, and design documentation for implantable neuromodulation systems.
• Translate needs into measurable system requirements, acceptance criteria, and traceable deliverables.
• Define system behaviors, interfaces, and architecture models across multidisciplinary teams.
• Collaborate with electrical, firmware, software, mechanical, clinical, and business teams to evaluate concepts and support integration.
• Support risk management, verification/validation, regulatory docs, design reviews, and commercialization.

Skills

Systems engineering

Requirements development

Cross-functional collaboration

Analytical thinking

Education

Bachelor's degree (Systems/Biomedical/Electrical/Software)

Tools

MBSE/SysML

Job description

Abbott in Plano, TX is seeking a Senior Systems Engineer for Neuromodulation. You will develop and maintain architectures for implantable neuromodulation systems, translate clinical and business needs into measurable system requirements, and collaborate with cross-functional teams to drive design tradeoffs and integration.

The role emphasizes risk management, verification/validation, and regulatory documentation in a regulated development environment, with opportunities for impact across patient