Position: NCR Specialist
Location: Kansas
Duration: 4 months, possible extension
Hours per week: 40
Start Date: May
Job Description:
Our client requires immediate assistance with a backlog of nonconformances (NCR’s) relative to medical device products. They need the consultant to hit-the-ground running by conducting on-the-floor investigations in order to rationalize cases that are put together for the NCR’s in order to apply necessary CAPA’s to close them out successfully. The initial project scope would involve reviewing SOP’s and being quickly assigned a weekly quota of NCR’s to close out (dependent on prior experience).
Candidates must display 3-5+ years of proven work history with:
Manufacturing & Quality Processes: cGMP/GDP process. Quality or manufacturing experience conducting investigations, CAPA’s, NCR’s, Root Cause Analysis.
Manufacturing Investigations for Medical Device and Pharma clients. Reviewing documents & processes to identify inconsistencies that may be leading to failures.
Root cause analysis tools & methods such as: Fishbone, Fault Tree, 5 Why’s, Comparative Analysis