development, detailed design, and design for manufacture for: medical and diagnostic devices, consumer personal electronics devices 3. Awareness of medical device processes and standards (ISO13485, 62304, 60601) 4. Experience in designing proof of concept (PoC) systems using Python/MATLAB and microcontrollers 5. Knowledge of machine learning and AI 6. more »
expanding the molecular products portfolio. The position holder will lead the technical development of new molecular reagents and associated methodologies, while working according to ISO13485 standards. The role may provide on a project need basis supervision for other team members, planning and coordinating various experimental work and … reagents, including PCR, isothermal amplification, and Next Generation Sequencing applications. Establish and disseminate technical knowledge and good laboratory practices in the group. Work to ISO13485 standards and understand their requirements. Independent planning, execution and troubleshooting of experiments. Write literature to support product launches. Keep accurate laboratory records. Assist with customers more »
s degree in relevant engineering discipline. Good communication and presentation skills 5 years experience (Min) in medical devices design and development with understanding of ISO13485 and IEC 60601 design control standards Multi-disciplinary engineering background (e.g., mechanics, electronics, software, data analysis and processing) with a generalist view more »
City of London, England, United Kingdom Hybrid / WFH Options
Newton Colmore
Ideally, the Medical Devices company you have worked for has produced handheld or portable Medical Devices, but as long as the device is to ISO13485 standards, we will consider your allocation. You will be rewarded with an excellent starting salary and package while being a part of more »
into the pharmaceutical market About Us: We are a specialized consultancy providing Regulatory Affairs support to the medical device industry. Our expertise spans across ISO13485, European regulations, FDA regulations, and other global standards for medical devices. Join our team and be part of a growing consultancy where more »
South West London, London, United Kingdom Hybrid / WFH Options
CURE TALENT LIMITED
to control other medical devices. Familiarity with FDA/MDR/UK MDR medical device software regulation is essential including applicable standards such as ISO13485, ISO 14971, IEC 62304, IEC 82304, and IEC 62366. Deep understanding of software development lifecycle (SDLC) and best practices in the more »
ll also develop prototype algorithmic functions based on data analysis and experimental findings. Additionally, you'll play a role in maintaining adherence to the ISO13485 quality management system and collaborate effectively with other engineers to support research and development initiatives and the overall project goal Better patient more »
