Description
CAPA Legacy Review, Product and Process Risk, ISO 13485, FDA
CAPA Legacy Review, Product and Process Risk, ISO 13485, FDA - My client requires an experienced CAPA Legacy Review Consultant for a long term contract. The following experience is a must.
* Strong knowledge of quality and compliance for Medical Device Industry (GMPs).
* Working knowledge of Quality System Regulations.
* A good working knowledge of related functions such as Operations, Supplier Management, Product Development and Procurement
* Experience in FDA QSR and ISO 9001/ISO 13485 standards, additionally a working knowledge of PAL and other related medical device national regulatory standards