Qualification:Bachelor or Master of E&E Engineering, E&TC Engineering, or equivalent with design background5-9 years of experience in Product developmentTechnical Requirements:Programming Tools: STM Cube IDE / STM 32, TouchGFXProtocols: SPI, I2C, BLE, ADC, DAC, UART, USB, Ethernet, PCIe, etc.Development Process: Agile, SCRUM, V Model, etcTools: Embedded C, C++, MATLAB, SimulinkEDA and PCB Design: Dip Trace, Eagle, AltiumProtocols: SPI,I2C, UART, USB, Ethernet etcResponsibilities:Logical algorithm for system architecture design and development.Develop and optimise firmware for STM32 microcontrollers, focusing on efficient and reliable operation of Medical Equipment components and systems.Design and implement motion controller firmware to ensure accurate and precise motion control for diagnostic instruments, utilising your expertise in motor control techniques.Collaborate with cross-functional teams including hardware engineers, software developers,and medical experts to design, develop, and test embedded software solutionsImplement SPI and UART communication protocols to facilitate seamless communication between various components of the diagnostic devices. Proficiency in debugging tools: Using debuggers, oscilloscopes, logic analyzers, and JTAG for troubleshooting and optimization.Own SDLC Process and Embedded Electronics design life cycle process of new, existingmedical equipments and its technology while focusing on product design, on-time updates & problem solving.Interact with clinicians, third-party vendors, manufacturers, sub-contractors, and direct reports to develop collaborative plans and complete projects.Experience:Experience in the Embedded software design lifecycle for sub-systems, comprising of high- speed electronics, High Speed integrated interfaces, and traceability to design requirements.Proficiency in communication protocols such as SPI and UART, with the ability to design and implement reliable communication interfaces.Experience working with real-time operating systems (RTOS) for embedded systems, ensuring timely and deterministic execution of tasks.Familiarity with medical device development standards and regulations (e.g., ISO 13485, IEC 62304) is a plus.Detail-oriented approach to writing clean, organised, and well-documented code.Prior experience in the medical device industry is advantageous but not mandatory.Role Type:Full Time, In-office, based out of our office in Bhiwadi.Should be ready to move anywhere in India or abroad.Should be ready to visit to Suppliers / Vendors and Customers if needed