> Markdown version of [/jobs/ext/3660863-sr-software-engineer](https://www.wearedevelopers.com/jobs/ext/3660863-sr-software-engineer). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Sr. Software Engineer - **Company:** FIELD MEDICAL, INC. - **Location:** Oceanside, CA, United States - **Experience:** Expert - **Contract:** Permanent contract - **Skills:** Software Applications, C++ (Programming Language), Computer Engineering, Linux, Embedded Software, Linux System Administration, Software Architecture, Qt (Software), Software Engineering, Systems Integration, Test Management, Scripting, Real Time Systems, Fpga Hardware, Information Technology, Meditech - **Published:** October 9, 2026 - **Apply:** https://www.disabledperson.com/jobs/75941095-sr-software-engineer ## About the Role * Bachelor's degree in Software Engineering, Computer Science, Computer Engineering, or related discipline * 5+ years of professional software development experience * Demonstrated experience developing Class III medical devices in heavily regulated environments * Comprehensive understanding of FDA regulatory requirements and ISO 13485 standards * Advanced proficiency in C++ and Qt framework * Strong experience with Linux operating systems * Proficiency in Python scripting for automation and testing * Experience with test management systems, particularly Helix * Willingness to participate in animal studies for preclinical device validation * Proven ability to work effectively in cross-functional, collaborative team environments * Demonstrated adaptability in dynamic, resource-constrained settings, * Experience with FPGA development and hardware-software integration * Prior experience in startup or early-stage company environments * Direct involvement in regulatory submissions (510(k), PMA, or IDE applications) * Knowledge of real-time systems and embedded software development * Familiarity with design control processes and quality management systems Location & Travel Requirements: * Hybrid * Willingness to travel up to 10% ## Description At Field Medical, we are looking for a hands-on Software Development Engineer with experience developing Class III medical devices. You will work directly with multidisciplinary teams to design, develop, test, and validate software for our medical device platform. This role combines software development, testing, and field support responsibilities in a fast-paced MedTech environment. Your Responsibilities Will Include: Software Development * Design, develop, and maintain software applications using Qt, C++, and Linux environments * Develop Python scripts for automation, testing, and system integration * Collaborate with hardware engineering, regulatory affairs, and clinical teams to deliver integrated solutions, demonstrating strong communication skills with both technical and non-technical stakeholders * Participate in software architecture decisions and conduct thorough peer code reviews, maintaining technical excellence while meeting stringent quality and compliance standards * Take ownership of software deliverables from conception through validation, working independently while keeping the team informed of progress and challenges Quality Assurance & Testing * Execute and develop comprehensive test cases to satisfy regulatory and validation requirements * Maintain test documentation and traceability within the Helix test management system with meticulous attention to detail * Log, track, and resolve software defects with rigorous attention to documentation and compliance requirements * Support design verification and validation activities throughout the development process, adapting to evolving requirements and priorities as the product matures Cross-Functional Collaboration * Provide technical support to our clinical trials and animal studies to ensure optimal device performance. * Collaborate with clinical personnel to gather performance data and user feedback, translating insights into actionable technical improvements * Work closely with our quality team to ensure compliance with FDA and ISO 13485 standards, contributing expertise to regulatory submissions and documentation * Navigate changing priorities in a dynamic startup environment, demonstrating adaptability by shifting focus between development, testing, documentation, and field support as organizational needs evolve * Build strong working relationships across all functional areas, fostering a collaborative culture that drives the company's mission forward