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.
Collabera El Segundo, California, USA Office
222 N Pacific Coast Hwy N 12th Floor, El Segundo, United States, 90245
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