Senior Systems Engineer - Medical Devices & CRM Programs

Abbott (abbottcareers2 board)

United States

On-site

USD 140,000 - 190,000

Full time

5 days ago
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Job summary

Abbott is seeking a senior systems engineer to lead programs and manage complex, novel integrations across disciplines. You will organize work, define behaviors, verify designs, and ensure product quality while balancing schedule and cost constraints.

You will serve as SME for designated systems, collaborate with cross-functional teams including Clinical, Regulatory, and Engineering, and drive verification, validation, and design control activities in line with FDA and ISO requirements.

Qualifications

  • Minimum 8 years progressively more responsible system engineering with product development experience.
  • Experience with electrical, electro-mechanical, software or biomedical technologies relevant to implantable systems.
  • Strong knowledge of ISO and FDA design controls and regulatory requirements.

Responsibilities

  • Leads programs with novelty and cross-disciplinary integration across teams.
  • Plans, frames problems, designs solutions, and verifies outputs within schedule and cost constraints.
  • Organizes work to deliver programs and guides the execution of assigned tasks.
  • Contributes as SME for designated systems and engages in broad cross-functional reviews.

Skills

Systems engineering
Cross-functional collaboration
Requirements analysis

Education

Bachelor's degree in Software Engineering or Computer Science
Master's degree in Biomedical Engineering or related discipline

Job description

Abbott is seeking a senior systems engineer to lead programs and manage complex, novel integrations across disciplines. You will organize work, define behaviors, verify designs, and ensure product quality while balancing schedule and cost constraints.

You will serve as SME for designated systems, collaborate with cross-functional teams including Clinical, Regulatory, and Engineering, and drive verification, validation, and design control activities in line with FDA and ISO requirements.

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