Description
A minimum of 3 years of validation experience is required in medical device industry - IQ, OQ, PQ
Work experience with CNC systems
Interacting with Vendor, EHS and various stake holders across multiple Value streams.
Preparation of validation documents CCP, RA, IQP, IQ report, OQP, OQ report, PV/PQ protocols & reports, Engineering trials, etc
Good Experience in PLM JDE, Adaptiv.
Good experience in Manufacturing processes
Good experience in Vendor Management
Support any lean management activities (line balancing, time studies, and others)
Ability to work independently and partner with a cross-functional team (R&D, Regulatory, Manufacturing, Maintenance and Purchasing)