Summary : Supports testing and validation activities for medical devices, ensuring compliance with regulatory...
to design control requirements per ISO 13485 and FDA 21 CFR Part 820.Execute Design Verification and Validation (DVV) protocols...
per ISO 14971 and 21 CFR 820 throughout the project lifecycle. Plan and perform design verification and validation (DVV...
and Validation (DVV) protocols, including test planning, execution, and reporting. Manage Change Management processes in compliance...
specifications determination Design validation & clinical evaluation oversight Prototyping & product testing Vendor correspondence...