Software Engineer II

About The Company
Tandem Diabetes Care is dedicated to creating innovative solutions that improve the lives of individuals living with diabetes. As a leader in the diabetes technology industry, Tandem designs, manufactures, and markets advanced insulin delivery systems that empower users to manage their condition more effectively. The company's human-centered approach to product development emphasizes user experience, safety, and regulatory compliance, ensuring that each product meets the highest standards of quality and reliability. With a team comprising individuals who are personally affected by diabetes, Tandem fosters a passionate and inclusive environment committed to making a meaningful difference in healthcare. The company’s portfolio includes the Tandem Mobi system and the t:slim X2 insulin pump with Control-IQ+ technology, which features an intelligent predictive algorithm that automates insulin delivery for better glucose control.
About The Role
We are seeking a talented Software Engineer II specializing in Embedded Firmware to join our dynamic Software Engineering team. In this role, you will be responsible for designing, developing, and testing embedded software applications that are integral to our insulin delivery devices. You will work independently to identify opportunities for software improvements and contribute to the testing and validation processes to ensure product safety and efficacy. Your responsibilities will include developing software components for user interfaces, communication protocols, and device control, as well as participating in design reviews and maintaining comprehensive documentation in compliance with regulatory standards such as FDA guidelines, ISO 13485, and IEC 62304. Collaboration with cross-functional teams, including software testing and product development, will be essential to ensure the successful delivery of high-quality, compliant software products. This role offers a hybrid/remote work environment within the United States, with regular schedules aligned to Pacific Standard Time.
Qualifications

• Bachelor’s degree in Engineering, Computer Science, or a related field, or equivalent experience
• Minimum of 2+ years of experience in embedded software development, preferably for medical devices
• Proficiency in C and Rust programming languages; familiarity with JavaScript is a plus
• Experience with formal software testing methodologies and test-driven development (TDD)
• Strong understanding of software design, development, and validation processes
• Knowledge of regulatory standards such as FDA guidelines, ISO 13485, and IEC 62304
• Excellent problem-solving, communication, and teamwork skills
• Ability to work independently with minimal supervision and adapt to changing priorities
• Good Documentation Practices (GDP) knowledge is preferred

Responsibilities

• Design, develop, modify, and test embedded software units in accordance with corporate and regulatory standards
• Develop and integrate software components for user interfaces, communication protocols, and device control functionalities
• Identify opportunities for process improvements and communicate proposals to management
• Contribute to software design specifications, interface descriptions, and documentation; serve as documentation owner for specific projects
• Assist in the development of software verification and validation protocols
• Participate in formal testing activities, including executing test plans and analyzing coverage
• Support software testing with utility and embedded software tools
• Maintain compliance with Design Control processes, participating in design reviews and maintaining design history files
• Manage source code effectively using SCM tools and procedures
• Collaborate with product engineers to diagnose and resolve build and deployment issues
• Attend and coordinate documentation for Software Review Board (SRB) processes
• Analyze software issues to identify root causes and implement corrective actions
• Collect and review process metrics, lessons learned, and recommend process improvements
• Ensure all activities comply with privacy, HIPAA, and other legal/regulatory requirements
• Perform other duties as assigned in support of product development and quality assurance

Benefits

• Competitive annual base salary ranging from $119,300 to $140,000, commensurate with experience and location
• Health insurance benefits including medical, dental, and vision coverage starting on day one
• Health savings accounts (HSAs) and flexible spending accounts (FSAs)
• Paid time off including 11 holidays and a minimum of 20 days of accrued paid leave annually
• 401(k) retirement plan with company match
• Employee Stock Purchase Plan (ESPP)
• Comprehensive wellness programs and employee assistance resources
• Remote and hybrid work options with equipment provided

Equal Opportunity
Tandem Diabetes Care is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based on age, disability, sex, race, religion, gender identity or expression, marital status, pregnancy, sexual orientation, or any other protected characteristic. All qualified applicants will be considered for employment based on merit and individual qualifications. We are dedicated to fostering a workplace where everyone feels valued and empowered to contribute to our mission of transforming diabetes care.