Role & Responsibilities: Collaborate with cross-functional teams including hardware engineers, software developers, and medical experts to design, develop, and test embedded software and FPGA solutions. Develop firmware for FPGAs from vendors such as Xilinx Zynq, Lattice Semiconductor, and Texas Instruments , including SoC implementations and hardware/software co-design . Optimize and implement image and video processing algorithms on embedded platforms and FPGA architectures. Integrate and support FPGA/ASIC-based ISP blocks , ensuring high performance and accuracy in medical imaging applications. Work with SoCs with integrated ISP (e.g., Qualcomm, NVIDIA Jetson, Ambarella, MediaTek) and manage interaction with hardware accelerators. Design and develop firmware for STM32 microcontrollers , with a focus on motion control , real-time responsiveness , and precision actuation . Develop and implement motion control algorithms, including PID control and motor driver integration, for high-precision diagnostic instruments. Implement and optimize communication protocols such as SPI and UART to support system communication and control flows. Utilize real-time operating systems (RTOS) or bare-metal firmware development for deterministic system behavior. Perform thorough testing, debugging, and optimization using tools like oscilloscopes , logic analyzers , and JTAG debuggers . Support product design lifecycle activities including requirements specification , firmware documentation , and design reviews . Preferred candidate profile: Education: Bachelors or Masters degree in Electrical Engineering, Computer Science, or related field. A Ph.D . is a plus for R&D or algorithm-intensive roles, particularly in imaging or signal processing. Professional Experience: 3+ years of hands-on experience in embedded firmware development with strong C/C++ proficiency. Proven experience with FPGA design using VHDL/Verilog , and development with tools like Vivado, Quartus, or Diamond. Experience working with STM32 microcontrollers , including development environments like STM32CubeIDE and IAR Embedded Workbench. Core Technical Expertise: Deep understanding of: SoC and camera architectures Memory hierarchy, DMA engines, cache control, and hardware accelerators Motion control techniques for motor and actuator systems Image Signal Processing (ISP) pipelines: demosaicing, AWB, AE, gamma, sharpening, etc. Familiarity with Linux kernel camera subsystems (e.g., V4L2) . Ability to optimize embedded code for performance, power, and latency. Desirable Knowledge Knowledge of medical device standards and regulations such as ISO 13485 and IEC 62304 . Familiarity with image quality tuning tools (e.g., Imatest, DxO Analyzer). Experience with real-time data acquisition, frame synchronization , and multithreaded image capture pipelines . Soft Skills Strong problem-solving and debugging skills in complex embedded systems. Excellent communication and collaboration abilities, with experience working in interdisciplinary teams .

Role Overview: We are seeking a highly detail-oriented and scientifically literate Technical Writer to join our growing team. The ideal candidate will play a critical role in preparing technical documents including patent applications, scientific manuscripts, regulatory documentation, whitepapers, and technical reports. You will work closely with R&D, legal, and product teams to translate complex scientific concepts into clear, concise, and legally sound content. Key Responsibilities: Draft, edit, and review patent applications , invention disclosures, and related IP documents. Prepare scientific manuscripts , posters, and technical reports for publication or submission. Collaborate with scientists, engineers, and legal counsel to gather technical data and translate it into accurate and readable content. Ensure documentation aligns with regulatory standards such as ISO 13485 , IVDR , and other relevant guidelines. Maintain accurate records of technical content and version control. Create SOPs, whitepapers, and user manuals as required. Review and update internal documentation and support regulatory submissions . Required Qualifications: Bachelor's or Masters degree in Mechanical Engineering , Electrical Engineering , Biomedical Engineering , Biotechnology , or related field. PhD is a plus. Proven experience in technical/scientific writing , especially in the medical device domain. Experience with patent writing or working with patent attorneys is highly preferred. Strong knowledge of IP laws , patent structure , and scientific publication protocols . Excellent written and verbal communication skills. Proficiency in MS Office and reference management tools (e.g., EndNote, Mendeley). Familiarity with regulatory frameworks (e.g., ISO 13485, IVDR, FDA) is an advantage. Preferred Skills: Prior experience in startups or early-stage product development . Familiarity with LaTeX , GraphPad , or scientific illustration tools. Understanding of laboratory workflows and diagnostics development.

Role & Responsibilities Collaborate with cross-functional teams to conceptualize, design, and develop mechanical components, automation systems, and robotics solutions. Design, prototype, and implement electro-mechanical systems, including automation subsystems and robotic mechanisms . Create detailed design documentation, including CAD models, drawings, specifications, and technical reports. Utilize CAD software (e.g., SolidWorks, AutoCAD, or equivalent) and simulation tools to model, analyze, and optimize mechanical and robotic designs. Conduct feasibility studies, including simulations and proof-of-concept testing, to evaluate automation and robotic solutions. Optimize designs for performance, reliability, manufacturability, and cost-effectiveness, with a focus on automating processes and enhancing productivity. Work closely with the electronics and software teams to integrate mechanical designs with embedded systems and control algorithms. Develop and maintain production documents, including bill of materials (BOM), assembly instructions, standard operating procedures (SOPs), and testing protocols. Provide technical support during the manufacturing and assembly process, ensuring smooth integration of automation and robotic components. Lead or contribute to troubleshooting and problem resolution for production and field-deployed systems. Stay abreast of industry trends, emerging technologies, and best practices in automation, robotics, and mechanical design. Contribute to continuous improvement initiatives to enhance system automation, design efficiency, and overall product quality. Preferred Candidate Profile Bachelor's degree in Mechanical / Mechatronics / Robotics / Automation Engineering or related field. 2-3 years of proven experience as a Mechanical Design Engineer, Automation Engineer, or Robotics Engineer, preferably in the Medical, Automotive, or Aerospace Industry. Strong proficiency in CAD software (e.g., SolidWorks) and experience with simulation tools (e.g., FEA, CFD, kinematic analysis). Hands-on experience in designing and developing robotic arms, actuators, and automated systems. Familiarity with sensors, actuators, motor control, and integration of hardware with embedded systems. Knowledge of manufacturing processes, including CNC machining, injection molding, and 3D printing. Excellent problem-solving skills and ability to work collaboratively in a team environment. Role Details Role: Design Engineer (Automation & Robotics) Department: Research & Development Employment Type: Full Time, Permanent Role Category: Engineering & Manufacturing Education UG: B.Tech/B.E. in Mechanical, Mechatronics, or Robotics Engineering