Requires experience in a Medical Device manufacturing environment with Quality System processes, utilizing Trackwise for quality records, and working with cross functional teams.
Job Description
- 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.
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