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# Senior Software Engineering Manager, Embedded Systems

- **Company:** Transmedics Inc
- **Location:** Andover, MA, United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Agile Methodology, C++ (Programming Language), Configuration Management, Static Program Analysis, Software Quality, Continuous Integration, Embedded Software, Real-Time Operating Systems, Software Engineering, PIC Microcontroller
- **Published:** October 8, 2026
- **Apply:** https://www.indeed.com/viewjob?jk=323bd1fb8fc4ea3d

## About the Role

* BS/MS in Software Engineering, Electrical Engineering, or equivalent.
 * 8+ years in real-time embedded software development.
 * 5+ years managing embedded software teams, including contractors or vendors.
 * Proven record delivering products and managing program schedules and milestones.
 * Medical device or regulated-industry software experience (IEC 62304, FDA, ISO 13485)., * Class II/III medical device experience, including PMA or 510(k) submissions.
 * Embedded architecture expertise in C/ C++, RTOS (e.g., QNX) and ARM/ PIC platforms.
 * Familiarity with CI/CD, static analysis, and medical device cybersecurity.
 * Agile experience within a design-controlled environment.
 * PMP or similar certification, a plus.
 * Strong communication and organizational skills.

## Description

We are seeking a Senior Software Engineering Manager, Embedded Systems, to lead the team building embedded software for the Organ Care System (OCS ). You will manage full-time and contract engineers, own program schedules and milestones, and ensure compliance with our engineering processes and medical device standards., * Lead, hire, and develop a team of full-time and contract embedded software engineers.

 * Manage contractors and vendors, including SOWs, deliverables, and performance.
 * Build and own program plans, schedules, milestones, and resource allocation; report status and risks to leadership.
 * Ensure the team follows the software lifecycle per FDA guidance, IEC 62304, ISO 13485, and ISO 14971.
 * Own software development, verification, and configuration management procedures and DHF deliverables.
 * Lead software risk management, field complaint investigations, and CAPA.
 * Support quality audits, FDA inspections, and regulatory submissions.
 * Provide technical direction on embedded architecture, design, and code quality.
 * Partner with Systems, Hardware, Quality, Regulatory, and Product teams on requirements and integrated timelines.
 * Perform other TransMedics tasks and duties as assigned/required.