San Jose CA United States Remote Principal Medical Device Development Engineer (Embedded) IRC304687

The Principal Medical Device Embedded Software Engineer will serve as a senior individual contributor responsible for the architecture, design, implementation, integration, and maintenance of embedded software for regulated medical devices. The role requires deep embedded‑development expertise combined with practical knowledge of medical‑device design controls, risk management, verification, traceability, and Design History File documentation. This is not a people‑management position; the successful candidate will lead through technical ownership, architectural decision‑making, mentoring, and cross‑functional influence.

Key Responsibilities

• Provide technical leadership for embedded software development and sustaining‑engineering activities.
• Design, implement, debug, test, and maintain embedded software and firmware for medical devices.
• Define and evolve embedded software architecture, component boundaries, interfaces, and data flows.
• Analyze legacy software to understand existing behavior, architecture, dependencies, and technical limitations.
• Resolve complex software, firmware, hardware‑integration, performance, reliability, and field issues.
• Translate system and product requirements into clear, testable software requirements and technical designs.
• Decompose system‑level requirements into embedded software components and interfaces.
• Ensure alignment between software requirements, architecture, detailed design, implementation, risk controls, and verification evidence.
• Participate in and lead technical reviews, software design reviews, code reviews, and root‑cause investigations.
• Collaborate with electrical and systems engineers on hardware‑software interfaces, sensors, communication protocols, diagnostics, and device behavior.
• Develop low‑level drivers, device‑control logic, hardware abstraction layers, communication components, and application‑level embedded functionality.
• Support integration between embedded devices and external systems such as middleware, host applications, hospital networks, or cloud services.
• Perform technical impact analysis for software changes, defects, anomalies, component updates, and cybersecurity vulnerabilities.
• Support software remediation by identifying gaps between documented requirements and implemented behavior.
• Create or update software lifecycle documentation required for the Design History File.
• Ensure complete bidirectional traceability between requirements, risks, design, code, tests, defects, and release evidence.
• Collaborate with V&V and Software Quality teams to define verification approaches and improve testability.
• Support unit, integration, system, regression, performance, reliability, and cybersecurity testing.
• Investigate field‑reported issues and support corrective and preventive actions.
• Support controlled software builds, releases, configuration management, and design changes.
• Contribute to product risk analysis and ensure that software‑related risk controls are properly implemented and verified.
• Support internal audits, regulatory inspections, and submission‑related activities.
• Mentor software engineers and promote effective embedded‑development and documentation practices.
• Identify architectural improvements and technical‑debt reduction opportunities.
• Drive continuous improvement of software engineering processes, tools, code quality, and development efficiency.

Required Qualifications

• Bachelor’s or Master’s degree in Computer Science, Software Engineering, Computer Engineering, Electrical Engineering, Biomedical Engineering, or a related technical discipline.
• Typically 10–15+ years of professional embedded software or firmware development experience.
• Demonstrated experience operating at Principal Engineer, Senior Staff Engineer, Software Architect, or equivalent technical‑leadership level.
• Strong hands‑on experience developing embedded software in C and/or C++.
• Experience developing software for regulated medical devices, IVD systems, healthcare products, or another safety‑critical regulated industry.
• Experience with the complete embedded software lifecycle, including requirements, architecture, design, implementation, integration, verification, release, and maintenance.
• Strong understanding of embedded‑system architecture and hardware‑software interaction.
• Experience debugging complex embedded systems using appropriate hardware and software tools.
• Experience developing and maintaining multithreaded, real‑time, or event‑driven embedded applications.
• Experience with embedded operating systems, embedded Linux, or real‑time operating systems.
• Experience with device drivers, hardware abstraction, communication interfaces, and peripheral integration.
• Strong understanding of software architecture, modular design, state machines, memory management, concurrency, and fault handling.
• Experience with source control, configuration management, code reviews, defect tracking, and controlled software releases.
• Ability to analyze and improve large or legacy embedded codebases.
• Experience producing high‑quality technical and software lifecycle documentation.
• Strong analytical, troubleshooting, and root‑cause‑analysis skills.
• Ability to lead technical work through influence without direct management authority.
• Excellent written and verbal English communication skills.

Preferred Qualifications

• Experience with point‑of‑care or in‑vitro diagnostic devices.

Practical experience with several of the following:

• IEC 62304; ISO 13485; ISO 14971; FDA Design Controls; FDA 21 CFR Part 820; FDA guidance for medical‑device software; IEC 62366‑1; FDA cybersecurity guidance; EU MDR or IVDR; secure software‑development lifecycle practices; medical‑device verification and validation.

Exciting Projects: Come take your place at the forefront of digital transformation! With clients across all industries and sectors, we offer an opportunity to work on market‑defining products using the latest technologies.

Collaborative Environment: You can expand your skills by collaborating with a diverse team of highly talented people in an open, laidback environment — or even abroad in one of our global centers or client facilities!

Work‑Life Balance: GlobalLogic prioritizes work‑life balance, which is why we offer flexible work schedules and opportunities to work from home.

Professional Development: We provide continuing education classes, professional certification and training (technical, soft skills, language, and communication skills) to help you realize your professional goals. Being part of a global organization, there are additional learning opportunities through international knowledge exchanges.

Excellent Benefits: We provide our employees with competitive salaries, health and life insurance, short‑term and long‑term disability insurance, a matched contribution 401K plan, flexible spending accounts, and PTO and holidays.

Note: GlobalLogic estimates the starting pay range for this role to be performed remotely in USA is $145,000 – $155,000 and reflects base salary only. This pay range is provided as a good faith estimate and the amount offered may be higher or lower.