Medical device manufacturer in the greater Knoxville, TN area is growing! Immediate need for a Quality Engineer to support Validations for new product introductions. The Quality Engineer will work with Process Validations and Equipment Qualifications in a GMP environment. The QE will work with Root Cause Analysis (RCA) and Corrective Actions Preventative Actions (CAPA) as well as 5 Whys, FMEA, fishbone, 8D control planning, etc.
Qualified candidates will have BS Engineering degree along with at least 2-3 years experience. Experience in FDA-regulated environment is a plus, but not necessary.
Excellent company that has been growing rapidly through acquisitions and new product development. The corporation operates multiple manufacturing facilities in the United States.
Relocation assistance is available.
Qualified candidates will have BS Engineering degree along with at least 2-3 years experience. Experience in FDA-regulated environment is a plus, but not necessary.
Excellent company that has been growing rapidly through acquisitions and new product development. The corporation operates multiple manufacturing facilities in the United States.
Relocation assistance is available.