Lead Hardware Engineer

Tata Elxsi works with leading medical device OEMs and technology companies for market research and human factor engineering, hardware and software engineering, verification & validation, regulatory standards & compliance requirements along with technologies such as artificial intelligence, cloud and IoT. Tata Elxsi’s Medical Device and Healthcare practice is ISO 13485 certified. KEY RESPONSIBILITIES: • Technical collaboration between the cross functional team and the client. • Compile and analyze customer requirements, work with the team to find solutions, and consolidate and analyze customer requirements. • Creating and assessing system concepts for cost-cutting projects. • Hardware system design for product realization & schematic creation. • PCB design in accordance with established procedures and expertise in high-speed PCB design. • Leading and taking part in design reviews. • Develop System test plan/procedure document according to the customer requirements. • Lead and mentor a team that would be involved project. • Design and test documentation as per the standards • Functional safety development based on customer’s requirements KEY JOB REQUIREMENTS: Experience: 8-13 years of Embedded product development along with exposure to team management /leading Education: Graduation in Electrical & Electronics / Electronics & Communication Engineering Skills & Competencies: Experience in 8/16/32 Microcontroller and its peripheral component selection. • Experience in interfacing electro-mechanical devices such as sensors and actuators • Experience in Motor control circuit design and testing • Strong analog and digital circuit design and in-depth troubleshooting skills • Communication Interface design: RS232, SPI, I2C, USB, Bluetooth /Wi-Fi etc • Knowledge of Display and camera interfaces • Extensive working experience with board and system level testing and verification • Good knowledge of hardware ecosystem, including manufacturing and commercialization • Experience with developing design & verification documents for medical domain to comply with IEC60601-X, 61010 • Knowledge of global quality for medical device (ISO 13485) • Knowledge of Design Failure Mode and Effects Analysis (DFMEA) • Knowledge on the compliance requirement & should support product regulatory compliance testing including EMC/EMI, CCC, UL, RoHS, etc. • Excellent verbal and written communication skills • Excellent MS Project, Excel, Word, Visio, and Power Point skills • Ability to work independently and manage a cross functional team Must Have: • Design for excellence viz. DFT, DFM, DFA • Hands On experience of with PCB design ECAD tools like Mentor graphics/Orcad/Altium etc. • Hands on experience with Simulation tools like LT spice, PSPICE or equivalent. • Hands on experience with lab tools DSOs, Multimeter, Signal generators etc Preferred Skills: ▪ Agility: Drive speed of decision making and actions ▪ Confidence to take on the world: Think Big and dare to try ▪ Transparency: Build trust through openness and sharing of information and resources ▪ Improve Collaboration: We all win when we work together ▪ Ownership: Demonstrate commitment, make it happen, do it well ▪ Nurture learning & Growth: Enable learning, capability, enrichment and growth of our people.