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Quality Engineer (Validations)
Knoxville, TN

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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 3 years experience in an FDA-regulated environment working with 21 CFR regulations and ISO-13485.
 
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. 


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