Jobs and Careers

Software Engineer, RIS (Medical Imaging Software)....(PREFERRED LOCATION: Duraham, NC)

United Statesfull_timeVerifiedPosted 28 May 2025

💰 $115,000/yr($96,446/yr – $115,000/yr)

About the role

Position Overview

This position is a member of the engineering team, developing software for medical information products to be located in the Raleigh/Durham, NC area.

Company Overview

At FUJIFILM Healthcare Americas Corporation, we’re on a mission to innovate for a healthier world, and we need passionate, driven people like you to help us get there. Our cutting-edge healthcare solutions span diagnostic imaging, enterprise imaging, endoscopic and surgical imaging, as well as in-vitro diagnostics.

But we don’t stop at healthcare; our Non-Destructive Testing (NDT) team harnesses advanced radiography solutions to keep transportation infrastructure, aerospace, and oil and gas assets safe and running smoothly.

Ready to innovate, collaborate, and make a difference? Join us and bring your big ideas to life while working in a dynamic, flexible environment that fuels your creativity and drive.

Our headquarters is in Lexington, Massachusetts, an inspiring healthcare research hub in a historic town.

Fujifilm is globally headquartered in Tokyo with over 70,000 employees across four key business segments of healthcare, electronics, business innovation, and imaging. We are guided and united by our Group Purpose of “giving our world more smiles.” Visit: https://www.fujifilm.com/us/en/about/region/careers

Job Description

Duties and Responsibilities:

Design and implement product features from internal and external customer requirements and clinical feedback.
Apply standard technologies to software design, implementation, and testing.
Work closely with other team members to coordinate assignments and communicate progress and/or difficulties.
Investigate and resolve complex runtime software issues received from varying sources in a timely manner.
Understand requirements both from user’s perspective and technical details.
Manage personal project priorities, deadlines, and deliverables.
Developing new and maintaining existing code and design.
Providing input, solutions, and recommendations.
Participate in design and code reviews and understand and enforce the importance of coding standards.
Troubleshooting complex problems.
Comply with all applicable U.S. Food and Drug Administration (U.S. FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all other applicable laws, regulations, and standards.

Qualifications:

BS or BE in Computer Science or related field.
5+ years of experience in software development.
Excellent verbal and written communication skills.
Proven problem-solving skills.
Strong software development discipline.
Design and development of complex software components.
Able to identify debugging strategies in complex software environments.
Skilled in investigation, diagnosis, and resolution of performance issues.
Familiar with requirements analysis, design control documentation, revision control, and use of bug tracking tools to ensure software quality.
Assertive team player with demonstrated initiative.
Ability to work independently and meet deadlines.
Ability to quickly learn our application and be able to maintain existing and develop new features.
Proven problem-solving skills.
Ability to work independently and meet deadlines.

Exposure to real-world product development that must include:

ASP.NET Webforms
Object Oriented Design and Implementation, using .NET Technologies
Thorough understanding of Model View Controller (MVC) and Model-View-ViewModel (MVVM) architecture patterns
Repository and Singleton design patterns
Client technologies for creating Responsive Web Design.
Experience in using Telerik ASP.NET Ajax Toolkit
Entity Relationship Modeling and Principles of Relational Database
Agile/SCRUM work practices

Language/Environment:

Required: