with ISO13485 or ISO 9001 The Medical Device Quality Inspection group is responsible for assuring that materials, activities..., processes, and specified conditions related to the daily device manufacturing, processing and packaging meet current GMP...
with ISO13485 or ISO 9001 The Medical Device Quality Inspection group is responsible for assuring that materials, activities..., processes, and specified conditions related to the daily device manufacturing, processing and packaging meet current GMP...
Summary Assemble and test medical device assemblies, final products, and accessories per the manufacturing... functional relationships with the Materials group as well as the Engineering group as required. Working Conditions: Clean...
for analyzing the product features, developing test parameters, testing for quality and repeatability, and authoring final test... procedures, plans and results for the Sustaining Engineering team. Test Engineer Responsibilities: Meet with the product...