Work Flexibility: Hybrid or Onsite

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 higher value services and productivity.Manage partnerships with vendors and SME’s as needed.Contribute to absorption of new technologies, processes and methods.Develop an open culture to instill confidence, diversity of perspectives and knowledge sharing and an environment to focus on customer needs.

What you will need:

Required-

B. Tech / B.E / M. Tech / M.S. – MechanicalExperience: 5-7 years

Preferred-

Strong analytical skillsEffective interpersonal skillsStrong communications skills

Travel Percentage: 10%