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.