Systems Engineer II - Medical Devices & Verification

Abbott Laboratories; Los Angeles (CA); On-site; USD 82,000 - 141,000; Full time

Job summary

Abbott Laboratories in Los Angeles, CA, is seeking a Systems Engineer to support product development of medical devices. The role involves defining and validating system requirements, evaluating algorithms, and coordinating cross-functional reviews.

Responsibilities include developing test frameworks, performing simulations/tests, and ensuring alignment with regulatory standards. Travel about 10% may be required.

Qualifications

• Bachelor's degree in Biomedical Engineering or related field or equivalent
• Master's degree in a relevant discipline preferred
• Minimum 2 years in medical product development with cross-functional experience

Responsibilities

• Lead defined tasks within a larger effort to ensure on-time, high-quality completion.
• Define system requirements for new algorithms and support transition into projects via clinical review.
• Gather and translate input requirements for medical devices into system specifications and interfaces.
• Simulate or test new projects/algorithms to verify performance and customer fit; conduct beta testing.
• Define system engineering requirements for new algorithms or features and facilitate transitions.
• Contribute to evaluation and verification of subsystems or projects prior to submission.
• Contribute to development of system verification plans and execution of tests.
• Develop and maintain automated test frameworks, scripts, and tools to improve efficiency.
• Interact with cross-functional groups for feasibility studies, benchmarking, or concept studies.
• Identify and resolve issues; escalate when needed.
• Support QMS/EMS regulatory initiatives and other company policies.

Skills

C#

Python

MATLAB

C++

Education

Bachelors in Biomedical Engineering or related field

Masters in a relevant discipline (preferred)

Job description

Abbott Laboratories in Los Angeles, CA, is seeking a Systems Engineer to support product development of medical devices. The role involves defining and validating system requirements, evaluating algorithms, and coordinating cross-functional reviews.

Responsibilities include developing test frameworks, performing simulations/tests, and ensuring alignment with regulatory standards. Travel about 10% may be required.