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What you will do :
• Product design & development; Understanding of regulations applicable to devices, particularly standards- including 21CFR820, ISO 13485 throughout the design and development process.
• Knowledge of material selection, International standards, and norms; Sheetmetal, Welding, Marking Methods like Laser marking, Engraving, Stamping, Silk screening, etc.
• Proficient in Pro-E; Concept design and development; dFMEA, DFM, Basic GD&T, Tolerance Stack-up.
• Understanding of biomedical and bio-mechanical engineering, or biomaterials; Basic inspection techniques, inspection methods;
• Knowledge of manufacturing process, engineering change process, Design Verification and Validation, Design and Risk Management documents; Blueprint/Engineering schematic reading and interpretation.
• Responsible for the timely and quality deliveries of the assigned tasks; Work as point of contact for all project related aspects with the stakeholders; Ensure continual improvement in delivering h ...