ViTAA Medical Solutions

www.vitaamedical.com

1 Job

29 Employees

About the Company

ViTAA's RAW(tm) (Regional Areas of Weakness) Mapping technology can analyze the deformation of the aorta wall using images captured throughout the cardiac cycle. Then, by incorporating critical simulation data on blood flow and location and size of clots (ILT or intraluminal thrombus) within the aneurysm, ViTAA's algorithms compute and generate detailed strength and weakness maps of the abdominal aortic aneurysm.

Listed Jobs

Company Name: ViTAA Medical Solutions
Job Title: Full-Stack Developer
Job Description: **Job Title:** Full‑Stack Developer **Role Summary:** Develop and maintain AI‑driven medical imaging software, including 3‑D visualization algorithms and user‑interface components, while ensuring compliance with FDA and ISO 13845:2016 quality standards. Collaborate with cross‑functional teams—research, clinical, regulatory, and quality assurance—to deliver robust, user‑focused solutions for vascular aneurysm diagnosis and treatment. **Expectations:** - 2‑5 years of professional software development experience. - Ability to translate clinical and scientific requirements into functional software. - Strong problem‑solving mindset with a focus on user needs and efficient delivery. - Commitment to adhere to medical device quality processes and documentation standards. **Key Responsibilities:** - Design, prototype, and implement static and dynamic 3‑D graphics algorithms for computational and visualization tasks. - Contribute to FDA‑compliant software quality processes; coordinate with regulatory and QA engineers. - Develop and refine user‑interfaces for clinical workflow integration. - Perform feasibility studies and prototype medical software components. - Execute general development duties: bug fixing, code updates, and maintenance. - Author SOPs, protocols, reports, and manuals per ISO 13845:2016. - Present technical findings and design reviews to stakeholders. **Required Skills:** - Proficient programming in at least one language (e.g., C++, C#, Java, Python, JavaScript). - Experience with 3‑D graphics libraries/frameworks (e.g., OpenGL, WebGL, Unity, Three.js). - Understanding of software development lifecycle and version control (Git). - Familiarity with FDA and ISO medical device software standards. - Strong communication skills for cross‑disciplinary collaboration and presentations. - Ability to produce clear technical documentation. **Required Education & Certifications:** - Bachelor’s or Master’s degree in Software Engineering, Computer Science, Systems Engineering, or a related field. - Knowledge of ISO 13845:2016 (medical device) standards; FDA software compliance experience preferred.