- 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.