Job Description

About the Role

Join our core project team and play a key role in quality engineering across the entire product development cycle for Class II & III medical devices. This position ensures compliance with global regulatory standards, drives risk management, and supports design assurance for innovative healthcare solutions.


Key Responsibilities

  • Lead product risk management, usability, reliability, and design validation for new product development and design changes
  • Develop and implement design verification & validation plans with project design leads
  • Define Critical to Quality (CTQs), design input/output documents, and ensure adherence to quality systems & SOPs
  • Manage ...

Apply for this Position

Ready to join Infosys? Click the button below to submit your application.

Submit Application