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IVANAE Medical

IVANAE Medical

ivanae-medical.com

1 Job

2 Employees

About the Company

IVANAE is a medical device company providing an innovative technology for contactless respiratory monitoring. Our mission is to:
• improve clinical prognosis in patients with respiratory diseases
• improve patients’ care and safety by adapting High-Flow Nasal Cannula (HFNC) therapy to the patient’s needs
• help health care providers diagnose by offering continuous measurement of respiratory parameters

Listed Jobs

Company background Company brand
Company Name
IVANAE Medical
Job Title
Software Engineer
Job Description
Ivanane Medical is a MedTech startup specializing in the development of innovative technologies for respiratory monitoring and treatment. As part of the development of its medical device, LunGuard, which integrates 3D imaging and artificial intelligence for non-invasive monitoring, we focus on real-time respiratory function monitoring for patients in intensive care units (ICUs). Effective respiratory monitoring plays a crucial role in tracking disease progression, optimizing therapeutic settings, and identifying factors contributing to ventilatory deterioration.

Main Mission:
Analyze the existing software, evaluate its architecture, optimize its performance, and ensure its compliance with the IEC 62304 standard within the integration of a medical device leveraging computer vision and artificial intelligence (AI) technologies.
Key Responsibilities:
‐ Study and document the current software architecture.
‐ Develop a refactoring and optimization plan to enhance code efficiency.
‐ Optimize existing computer vision and AI algorithms.
‐ Develop and integrate new features following best software development practices.
‐ Ensure the software meets the required performance and security standards
‐ Adapt the development lifecycle to ensure traceability and risk management.
‐ Write and maintain technical documentation (specifications, test reports, anomaly management).
‐ Work closely with quality assurance (QA) teams to ensure regulatory compliance.
‐ Design and execute unit, integration, and validation tests.
‐ Participate in code reviews and internal audits to ensure software quality.
‐ Define the training protocol and algorithm verification plan.

Required Profile:
Master’s degree (Bac+5) or equivalent in computer science, image processing, artificial intelligence, or any related field.
Experience in software development.
Experience in medical devices is a plus.

Technical Skills:
Proficiency in C++ and Python.
Strong expertise in computer vision (OpenCV, TensorFlow, PyTorch, or similar).
Knowledge of Agile development methodologies.
Experience in AI and machine learning.
Familiarity with regulatory requirements and cybersecurity standards for medical devices.
Experience with version control tools (e.g., Git).
Strong technical writing skills for regulatory documentation (test plans, risk analysis, software specifications, architecture documentation).
Brest, France
Hybrid
21-02-2025