Bramhanand Dhamanekar

Results-driven engineer with a robust background in mechanical engineering, coupled with 3 years of experience in the medical device and aerospace industries.Dedicated regulatory affairs professional with expertise in CE marking, ISO 13485, Medical Device Regulation, FDA, ISO, EU MDR requirements, and IEC design controls.A design engineer well-equipped with CAD tools like CATIA and SolidWorks.

Streamlined manufacturing processes, resulting in a 20% reduction in production time through optimized machining sequences and setup sheets Proven track record in identifying and mitigating failure modes and enhancing design processes for superior quality and precision. Conducted design reviews and failure mode and effects analyses (FMEA)