Principal Software Engineer - Urology R&D

About the Role

Key Responsibilities

• Architect, design, develop, and release high-performance medical device software solutions.
• Prototype and implement efficient, maintainable solutions using modern C++ (C++11 or newer).
• Provide technical leadership in software architecture, design, and industry-leading development practices.
• Collaborate cross-functionally with marketing, systems engineering, QA, hardware, and regulatory teams to translate requirements into robust solutions.
• Mentor a high-performing team of software engineers, fostering technical growth and accountability.
• Drive the full software development lifecycle, including requirements definition, planning, design, code reviews, and documentation.
• Foster a collaborative engineering culture that encourages pragmatic decision-making and shared ownership.
• Identify and implement continuous improvements to development processes, tools, and workflows.
• Support clinical staff in the field by troubleshooting and resolving software-related issues in real-world use.
• Demonstrate a strong commitment to building innovative products that save and improve lives.

Requirements

• Bachelor's degree in Computer Science, Computer Engineering, Software Engineering, Electrical Engineering, or a related technical discipline.
• Minimum of 8 years of professional software development experience, with proficiency in coding using multiple programming languages.
• Minimum of 3 years of software development experience in a regulated, technology-focused industry.
• Proven ability to lead projects through the full software development lifecycle using Agile methodologies and project management practices.
• Experience with networking and cybersecurity principles.
• Expertise in deploying, customizing, and securing Linux operating systems.
• Proficiency in C++ (C++11 or newer), with experience in developing coding standards and secure coding practices.

Nice to Have

• Strong verbal and written communication skills.
• Demonstrated ability to lead cross-functional teams and influence technical direction.
• Strong problem-solving abilities and adaptability in a collaborative team environment.
• Experience with software configuration management tools, including source code control (e.g., Git), issue tracking (e.g., Jira), requirements management (e.g., Cockpit), and code review tools (e.g., Code Collaborator).
• Experience working in the medical device industry.
• Familiarity with medical device regulatory standards, including IEC 62304, IEC 60601, FDA 510(k), ISO 14971, and ISO 13485.
• Knowledge of cybersecurity best practices and standards.

Qualifications

• Educational background as specified in requirements (e.g., Bachelor's degree in relevant technical field).

Benefits & Perks

• Competitive salary range from $103,700 to $197,000, commensurate with experience.
• Potential variable compensation including bonuses and incentives.
• Supportive work environment with access to latest tools, information, and training.
• Opportunities for career advancement and skill development.
• Inclusive and diverse workplace culture.