Elixir
Entry-Level Software Engineer
About Us
ELIXIR MD Inc. is a dynamic and rapidly expanding medical device innovator, proudly based in Irvine, CA. Our commitment to a Made in the USA ethos drives our global operations, with sales in 22 countries and counting. Our cutting-edge flagship device is revolutionizing the practice of plastic surgery around the world. In light of our ongoing growth and the increasing complexity of our product offerings, we are seeking a full-time Entry-Level Software Engineer to help us elevate our operations with creativity and precision.
Role Description
The Entry-Level Software Engineer at ELIXIR MD plays a vital role in designing, developing, testing, and deploying software applications that seamlessly integrate with our innovative medical technologies and operational systems. Your contributions will be key in creating scalable and compliant software solutions for both Microsoft and Apple environments, focusing on data integrity and exceptional user experiences.
Key Responsibilities
Assist in developing and maintaining software solutions for internal and client-facing systems across platforms.
Collaborate closely with senior engineers to design APIs, databases, and user interfaces tailored to ELIXIR MD's technology ecosystem.
Write clean, maintainable code in languages such as
C#, Swift, Python,
and
JavaScript . Support software validation and verification activities in compliance with
FDA 21 CFR Part 11
and
ISO 13485
standards. Conduct unit and integration testing to guarantee software reliability and performance. Work together with IT and Clinical Operations to ensure system interoperability and uphold cybersecurity. Participate in agile development sprints, version control processes using GitHub or Azure DevOps, and maintain release documentation. Provide technical support during software deployment and troubleshooting, while gathering user feedback. Collaborate with UI/UX and data teams to enhance functionality and visual aesthetics for both Windows and macOS/iOS applications. Qualifications Proficient in the
Microsoft stack : C#, .NET, Visual Studio, Azure, SQL Server, Power BI. Experience with
Apple development tools : Swift, Xcode, iOS SDK, and macOS integration. Familiarity with
cross-platform frameworks
(e.g., Xamarin, .NET MAUI, React Native). Understanding of
API design
(REST/GraphQL) and data security principles (OAuth, SSL/TLS). Experience with
cloud environments
(Azure, AWS) and CI/CD pipelines. Knowledge of
GxP software validation
and documentation processes is a plus. Strong analytical skills combined with a detail-oriented approach to problem-solving and debugging. Excellent communication abilities to effectively collaborate within multidisciplinary teams. Curiosity and adaptability in learning within a regulated medical technology environment. Exhibit integrity, accountability, and the initiative to drive projects forward. Education & Experience Bachelor's degree
in Computer Science, Software Engineering, Information Systems, or a related field. Up to 2 years of software development experience, including internships or significant project work. Exposure to the
medical device, biotech, or regulated technology
industry is preferred. Familiarity with
Agile development methodologies
and
version control tools
(Git, Azure DevOps). This position is office-based in Irvine, California. We invite passionate individuals eager to grow and contribute to an exciting team to apply today.
C#, Swift, Python,
and
JavaScript . Support software validation and verification activities in compliance with
FDA 21 CFR Part 11
and
ISO 13485
standards. Conduct unit and integration testing to guarantee software reliability and performance. Work together with IT and Clinical Operations to ensure system interoperability and uphold cybersecurity. Participate in agile development sprints, version control processes using GitHub or Azure DevOps, and maintain release documentation. Provide technical support during software deployment and troubleshooting, while gathering user feedback. Collaborate with UI/UX and data teams to enhance functionality and visual aesthetics for both Windows and macOS/iOS applications. Qualifications Proficient in the
Microsoft stack : C#, .NET, Visual Studio, Azure, SQL Server, Power BI. Experience with
Apple development tools : Swift, Xcode, iOS SDK, and macOS integration. Familiarity with
cross-platform frameworks
(e.g., Xamarin, .NET MAUI, React Native). Understanding of
API design
(REST/GraphQL) and data security principles (OAuth, SSL/TLS). Experience with
cloud environments
(Azure, AWS) and CI/CD pipelines. Knowledge of
GxP software validation
and documentation processes is a plus. Strong analytical skills combined with a detail-oriented approach to problem-solving and debugging. Excellent communication abilities to effectively collaborate within multidisciplinary teams. Curiosity and adaptability in learning within a regulated medical technology environment. Exhibit integrity, accountability, and the initiative to drive projects forward. Education & Experience Bachelor's degree
in Computer Science, Software Engineering, Information Systems, or a related field. Up to 2 years of software development experience, including internships or significant project work. Exposure to the
medical device, biotech, or regulated technology
industry is preferred. Familiarity with
Agile development methodologies
and
version control tools
(Git, Azure DevOps). This position is office-based in Irvine, California. We invite passionate individuals eager to grow and contribute to an exciting team to apply today.