- Location
- US - Massachusetts (Acton - Office), United States of America
- Workplace
- Hybrid
- Type
- Full-time
- Department
- Engineering
- Seniority
- Senior
- Education
- Master
- Closing date
- Today
- Source
- Workday
Description
Job Summary
This role is responsible for supporting embedded software development for Insulet's medical devices throughout the entire software lifecycle, including design, development, testing, maintenance, and continuous improvement. The ideal candidate is a collaborative and adaptable engineer who takes ownership of team priorities, contributes across multiple areas, and works effectively in a regulated, cross-functional environment to deliver high-quality software solutions.We are looking for a collaborative and adaptable Staff Software Engineer to join the Life Cycle Engineering (LCE) team supporting Insulet's embedded software for medical products. This role contributes across the full software lifecycle—including design, implementation, testing, documentation, maintenance, and continuous improvement—in a regulated, multidisciplinary environment.
Success in this role means taking ownership of the work needed by the team, whether that involves new feature development, defect resolution, design documentation, test support, or cross-functional integration. We value engineers who communicate openly, bring positive energy to the team, and approach every assignment as an opportunity to strengthen the product and help teammates succeed.
Responsibilities:
- Design, develop, test, document, and maintain embedded software for new and existing Insulet products
- Own assigned work end-to-end—including implementation, debugging, documentation, and verification—with a strong commitment to quality, completeness, and successful delivery
- Analyze, troubleshoot, and resolve complex software and system issues spanning multiple components, disciplines, or product generations
- Apply sound engineering judgment to evaluate technical tradeoffs, investigate root causes, and drive issues to resolution with minimal supervision
- Ensure software designs and development activities comply with company policies and applicable regulatory requirements for medical devices.
- Create and maintain design documentation, requirements, and test artifacts as a routine part of engineering work
- Partner with Quality, Regulatory, Marketing, Manufacturing, and other cross-functional teams to ensure solutions meet technical, regulatory, and business requirements.
- Collaborate closely with software, software quality, and hardware engineers to integrate, debug, and test system functionality.
- Participate constructively in design reviews, code reviews, and team planning; share knowledge and help teammates succeed.
- Adapt to changing team and product priorities by contributing across development, maintenance, and support activities as needed.
- Provide technical leadership when appropriate, helping guide design decisions, mentor team members, and drive technical excellence.
- Perform other duties as required.
Basic Requirements:
- Bachelor's degree in software engineering, Computer Science, or a related field and 10+ years of relevant work experience; or a master's degree in related field and 8+ years of relevant experience.
- Strong programming skills in C and/or C++.
- Hands-on experience with Embedded Systems
- Experience developing embedded software for ARM, TI, MSP, or similar microcontroller-based systems is required
- Demonstrated ability to contribute effectively on a shared codebase and collaborate with internal and external team members
- Willingness to lead technically when needed — mentoring, reviewing, or guiding an area of the design — while remaining hands-on and team-oriented
- Knowledge of I2C, SPI, Flash, EEPROM and/or USB
- Familiarity with communication systems and/or wireless protocols (BLE a plus)
- Medical device or other regulated-industry experience
- Knowledge of OS concepts (threading, mutual exclusion, interrupts, deadlock avoidance)
- Understanding of RTOS and real time systems
- Object-oriented design where applicable
- Ability to read electrical schematics
- Familiarity with Agile or other SDLC practice
Physical Requirements:
- General office environment, may sit for long periods of time
Additional Information:
Insulet Corporation (NASDAQ: PODD), headquartered in Massachusetts, is an innovative medical device company dedicated to simplifying life for people with diabetes and other conditions through its Omnipod product platform. The Omnipod Insulin Management System provides a unique alternative to traditional insulin delivery methods. With its simple, wearable design, the tubeless disposable Pod provides up to three days of non-stop insulin delivery, without the need to see or handle a needle. Insulet’s flagship innovation, the Omnipod 5 Automated Insulin Delivery System, integrates with a continuous glucose monitor to manage blood sugar with no multiple daily injections, zero fingersticks, and can be controlled by a compatible personal smartphone in the U.S. or by the Omnipod 5 Controller. Insulet also leverages the unique design of its Pod by tailoring its Omnipod technology platform for the delivery of non-insulin subcutaneous drugs across other therapeutic areas. For more information, please visit insulet.com and omnipod.com.
We are looking for highly motivated, performance-driven individuals to be a part of our expanding team. We do this by hiring amazing people guided by shared values who exceed customer expectations. Our continued success depends on it!
At Insulet Corporation all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.