Medical Device Systems Engineer Intern

Acist Medical Systems Inc.; Eden Prairie (MN); On-site; USD 32,000 - 34,000; Full time

Benefits offered by this job

Time off

Medical benefits

On-the-job learning

Job summary

Bracco Medical Technologies is seeking a Systems Engineering Co-op/Intern to support definition, analysis, and validation of medical devices used in interventional cardiology and diagnostic imaging.

You will work with a senior systems engineer and cross-functional teammates, learning systems engineering practices and applying them throughout medical device development, with responsibilities spanning requirements, testing, and traceability.

Qualifications

• Two years of study toward a bachelor's degree in engineering or scientific discipline.
• Enrolled in biomedical, electrical, mechanical, software, or systems engineering program.
• Experience with requirements and test management tools such as Jama.

Responsibilities

• Define user needs, system and sub-system requirements, and system architecture.
• Develop and perform testing to support architectural decisions and system characterization.
• Remediate requirements to align with architecture of fielded medical devices.
• Create traceability between system artifacts using requirements/test management tools.
• Partner with team to diagnose product issues.
• Perform trade-off analyses to aid technical decisions.
• Acquire, analyze, and report results for product testing and reliability data.

Skills

Biomedical engineering

Electrical engineering

Mechanical engineering

Software engineering

Systems engineering

Jama (requirements tools)

Education

Two years toward a bachelor's degree in engineering or a scientific discipline

Tools

Jama

Job description

Bracco Medical Technologies is seeking a Systems Engineering Co-op/Intern to support definition, analysis, and validation of medical devices used in interventional cardiology and diagnostic imaging.

You will work with a senior systems engineer and cross-functional teammates, learning systems engineering practices and applying them throughout medical device development, with responsibilities spanning requirements, testing, and traceability.