Senior Software Engineer

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%