Quality Analyst Intern; Software

Why Join Bracco Medical Technologies?

We care as much about our employees as we do our patients. Our culture fosters a work environment where employees can thrive, be passionate and have fun along the way. Each member of the Bracco Medical Technologies team has the power to make a difference......every day!

At Bracco Medical Technologies, every employee has an impact on our Mission to empower lifesaving decisions. We create medical devices that give healthcare providers the insights they need to confidently and safely diagnose patients. Our unique line of products includes Intravascular Ultrasound (IVUS), Fractional Flow Reserve (FFR), Cardiovascular Imaging contrast delivery (CVi), and CT and MRI contrast delivery systems. As part of the Bracco Group, Bracco Medical Technologies benefits from the resources of a multinational conglomerate with broad expertise in cath lab and radiology suite technology and a dedication to continuous advancement.

We are currently seeking an intern to learn and engage in a variety of hands‑on projects alongside our Quality team.

The Quality Analyst Intern (Software) will report to a Quality Analyst, working in the focused area of software development compliance. This will cover key development and testing requirements that need to be met in a regulated environment. You will also be exposed to working with different elements of the Quality System at Bracco Medical Technologies (BMT). This will involve equipment, methods and concepts within the industry.

This role will provide the opportunity to develop knowledge and gain experience for future Quality careers, including building your professional network.

• Quality Concepts
• Interpretation of SOPs
• Aspects of project lifecycle management processes, and navigating a PLM system
• Interpretation of key quality elements followed in product development
• Requirements management, Test case traceability, Risk analysis
• Enhancing product reliability and performance.
• Software development standards, regulations, and engineering practices that meet FDA requirements.

• Complete reviews on technical reports, test protocols, assorted documents related to software development
• Review and analyze risk assessments to determine probability of injury, data loss, etc.
• Compile review summaries
• Provide peer review / feedback on others’ work efforts
• Support innovation initiatives e.g improving traceability methods
• Contribute to optimizing and streamlining current program processes
• Complete assigned projects related to program development related to validation activities
• Contribute to system rollover readiness
• Generate standard and ad‑hoc reports

• This is an interdisciplinary role; undergraduate pursuing a bachelor’s degree in biology, Accounting, Business, Biomedical, Computer Sciences.
• Other fields would also be considered.
• Basic, effective technical writing and presentation skills.
• Deadline‑based prioritization and task handling.
• Detail‑oriented.
• Ability to see individual components of a bigger picture.
• Preferred Analytical and problem‑solving skills.
• Lab testing or research experience.
• Above‑average interest in the life sciences.
• Intermediate‑level experience with Office tools like Excel, Visio, Powerpoint or similar.
• Familiarity with development life cycles and processes.
• Experience with constructing simple queries for reports.

Eden Prairie, Minnesota

Late May 2027 start date preferred

Hours:

40 hours per week

To learn more about Bracco Medical Technologies, please visit our website at:

Bracco Medical Technologies is an equal opportunity/affirmative action employer.

Estimated Pay Range:
Und…