CAPA Legacy Review, Product and Process Risk, ISO 13485, FDA

Job type:
on-site
Start:
Immediate
Duration:
7 month
From:
Darwin Recruitment
Place:
Basel-Stadt
Date:
11/21/2013
Country:
flag_no Switzerland
project ID:
630725

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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