• Experience in a Medical Device manufacturing environment working with Quality System processes such as Corrective and Preventive Action (CAPA).
• Experience using Trackwise software for tracking of quality system records. 4 year degree required Experience working with cross functional teams to identify and address quality issue root causes. 
• Experience and ability to produce clear, concise quality records. Ability to articulate information when communicating with others.
  

All your information will be kept confidential according to EEO guidelines.