Description
The Senior Quality Engineer will be responsible for the following:-supporting GNE Registration, launch and maintain production
-execute improvements and processes complaints with ISO 13485, 21CFR820, 21CFR
-development and implementation of statistical incoming and in process sampling/control plans
-develop process for supplier data submission to reduce internal inspections
-facilitate communication between quality engineering and manufacturing teams
-determine validated process effectiveness and lead continual development of system
The Senior Quality Engineer must meet the following requirements:
-B.S. in engineering field
-minimum of 7 years of experience in the industry
-strong leadership skills and ability to delegate tasks effectively
-capability to manage large scale projects and programs
Apply now for competitive rate, excellent benefits and the opportunity to work for a leading medical device company.