This position reports to a Software Development Lead. It contributes to the continued development of medical device software. This includes a Bluetooth-connected therapy device, its control applications on smartphones/tablet, and cloud-based backend technologies.  The ideal candidate will be comfortable working across those subsystem boundaries in collaboration with other cross-functional research and development teams. 

Responsibilities:

• Contributing to the development of a patient-facing Android app, a clinician-facing Windows GUI, and embedded software for the Bluetooth-connected therapy device
• Participate in all phases of the software development process, including requirements definition, implementation, and verification
• Collaborate with Product Management, Project Management, System Engineering, Research, and Usability Engineering to improve our SW products
• Generate and maintain relevant software documentation 
• Technology selection to meet evolving product requirements and SW platforms
• Other duties may be assigned at the discretion of the manager

Education / Experience Requirements:

• BS Degree in computer science, electrical engineering, or related field
• 2 years of graduate-level coursework and/or experience in software product development
• 2 years of experience using C#
• 2 years of experience with development environments, debugging tools, git, test automation, and defect tracking tools
• 1-year Android app development
• Good understanding of cybersecurity in mobile devices
• Strong written and verbal skills

Additional Preferred Knowledge, Skills, Abilities:

• Experience with the Xamarin framework
• Bluetooth communication on Android, Windows, or iOS
• C/C++ on SoC-based platforms (ESP32, Nordic nRF52, or similar ARM-based MCUs)
• Salesforce Health Cloud platform
• Knowledge of NoSQL databases (ideally Couchbase)
• Web technologies (REST APIs, JSON)
• Experience with the concepts and development of Software as Medical Device (SaMD) and Mobile Medical Applications (MMA), as defined by FDA.
• Experience with FDA, 21CFR820, ISO 13485, IEC 62304, and regulatory submission of Class III Medical Devices a plus