Director, Embedded Software Development

Director of Embedded Software Development The Director of Embedded Software Development is a senior leadership role responsible for strategy, architecture, development, and regulatory compliance of firmware and embedded software. As a leader, this individual will lead, mentor, and scale embedded software/firmware engineering teams ensuring that the software is safe, secure, and reliable. Responsibilities Define and execute the embedded software engineering vision, roadmap, and technical architecture for the medical device product portfolio. Recruit, mentor, and retain top‑tier talent, fostering a culture of innovation, excellence, and collaboration. Ensure compliance with regulatory standards, overseeing the creation of documentation for regulatory submissions. Guide the embedded design (C/C++), including RTOS‑based applications, control algorithm integrations, and hardware interfaces (SPI, I2C, UART, USB, Ethernet, etc.). Support technology innovation and clinical data collection projects as required in conjunction with internal teams. Partner with hardware, applications, product management, and clinical teams to optimize system performance and meet user needs. Contribute to cybersecurity threat modeling and risk management for medical devices. Manage schedules, budgets, and resources across multiple projects, utilizing agile methodologies. Qualifications Bachelor’s degree in an Engineering discipline preferred, or equivalent medical device development and leadership experience. 10+ years in embedded software development, with significant experience in regulated industry environments, preferably medical devices. 8+ years in an engineering management role, leading engineering and technical teams. Strong proficiency in C/C++ in a Linux/RTOS environment, as well as microcontrollers and low‑level drivers. Deep understanding of IEC 62304, ISO 14971, and FDA software development and validation requirements. Experience with CI/CD Build Pipelines and target testing methodologies for medical devices. Expertise in cybersecurity protocols and safety‑critical system development. Proven ability to work with external vendors and partners. Excellent communication skills, conveying technical concepts to non‑technical stakeholders. Occasional travel to vendors and customer sites may be required on an as needed basis. Travel: Occasional travel to vendors and customer sites may be required. Workplace: Minimum of 4 days of in‑office presence per week. Compensation $179,200.00 – $322,500.00 USD Annual. Location USA, CA – Irvine, Laguna Canyon. EEO Statement Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics. #J-18808-Ljbffr