About this opportunity
Field Medical lists this Sr. Software Engineer opportunity in carlsbad, California. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Company Overview:
Founded in 2022, Field Medical Inc. is a medical device company advancing next-generation pulsed field ablation (PFA) technologies for the treatment of cardiac arrhythmias.
Field Medical's flagship innovation, the FieldForce™ Ablation System, is the first contact force focal PFA catheter system designed specifically for ventricular use. By delivering brief, high-intensity electric fields to target cardiac tissue without thermal damage, the system represents a novel approach to treating some of the most challenging arrhythmias. The company’s proprietary FieldBending™ technology enables precise and large-volume lesion creation, supporting a broad range of electrophysiology applications.
About the Role:
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
Required Qualifications:
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
Preferred Qualifications:
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%
Field Medical, Inc. is proud to be an equal opportunity employer. We are committed to creating an inclusive and respectful workplace where everyone has the opportunity to thrive. All employment decisions, including recruitment, hiring, assignments, promotions, compensation, and other aspects of employment, are made without regard to race, color, religion, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, age, disability, veteran status, or any other protected status.
At Field Medical, we believe that diverse perspectives fuel innovation—and we’re proud to foster a culture where all voices are valued.
Worksite address
carlsbad, CA, 92002, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.