The primary purpose of the position is inspecting materials and products, and following documented ISO processes and procedures for meeting customer specific requirements. To comply with all necessary regulatory, quality system and business requirements as based on ISO 13485 and FDA requirements for medical device and Food manufacturing. Reporting to the site Quality Supervisor, the person will need to work closely with the Account Teams, Quality Engineers, Materials Department and any other groups as necessary.
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Job Type
Full-time
Career Level
Entry Level
Education Level
High school or GED
Number of Employees
5,001-10,000 employees