A highly successful, commercial-stage MedTech enterprise that develops advanced life-saving medical devices designed for real-time field deployment.
FDA-approved and backed by a robust portfolio of global paying clients, the company engineers mission-critical technology that impacts patient outcomes directly at the point of care.
The organization combines innovative software development with cutting-edge hardware design, maintaining high regulatory compliance and operational excellence standards.
The headquarters is based in a central tech hub (highly accessible, situated directly along the main transit network), operating under an in-office collaboration model.
Position Overview-
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Lead Embedded Software Engineer joining a high-caliber R&D group to drive the architecture, development, and evolution of life-saving medical systems.
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Developing and leading robust, low-level firmware architectures written primarily in C, seamlessly bridging the gap between sophisticated software layers and custom physical hardware.
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Guiding the entire product development lifecycle from conceptual system brings-up, physical board initialization, and hardware-software integration to final verification and validation (V&V) procedures.
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Authoring meticulous technical documentation, code architectures, and standard compliance frameworks conforming to strict international regulatory bodies.
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Interfacing closely with electronic layout designs, working with laboratory measurement equipment, and ensuring exceptional system reliability.
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Core Domain & Ecosystem- Embedded Software Engineering, MedTech & Medical Devices, Real-Time Systems, C Firmware Development, Hardware-Software Co-Design, System Bring-up, Integration, Verification & Validation (V&V), Technical Regulatory Documentation (FDA standards).
Requirements-
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Academic Background: B.Sc. in Electrical Engineering, Electronics Engineering, or a closely related quantitative field – Mandatory
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Strong professional background (extensive experience) dedicated strictly to core Embedded Software Development, with an emphasis on low-level programming – Mandatory
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Production-grade programming mastery in C – Mandatory
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High proficiency in English, with excellent technical writing and documentation capabilities – Mandatory
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Hands-on experience with system bring-up, multi-system integration, and structured Verification & Validation (V&V) testing methodologies – Strong Advantage
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Prior professional experience engineering systems under medical device standards or other highly regulated environments (e.g., FDA, CE) – Strong Advantage
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Technical familiarity with hardware/electronics design principles, circuit schematics, or CAD software (Altium Designer) – Advantage
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Scripting or test automation capabilities utilizing Python – Advantage