I am working in the Research & Development , QA & RA in Active and passive medical device manufacturing industry for 7 years. And also I am TUV SUD certified Auditor ISO 13485:2016 and I have hands on experience in Medical device R&D, QMS, ISO 14971, IEC 60601, IEC 62366 , MDR 2017/745, IMDR, SFDA and other medical device regulations. I have trained 10000 + students. I am familiar with 7 + design softwares . All over my industry experience is based on design and development. I have familiar with the product design, tool design, Ergonomics , simulation engineering, fixture design, packaging design.