Type & Duration : Contract | 06 Months
- Responsible for assuring that materials, activities, processes, and specified conditions related to the daily device manufacturing, processing and packaging meet current GMP standards and comply with applicable procedures and standards such as ensuring the quality integrity of the product.
Essential Functions :
Performs one of three functions in the Quality department :Inspecting raw materials to meet production requirementsConducts in-process inspection of manufacturing product and processesReviews final documentation and shipment packaging for medical devices, subassemblies, and kits.Education / Experience / Skills :
High School diploma or equivalentOne year's experience in a regulated work environment preferredKnowledge of FDA Quality System Regulations and ISO13485 pertaining to medical device manufacturing.