Quality Inspector - 1st Shift
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About The Position
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. All job responsibilities are to be performed in accordance with the company's Mission/Values Statement and its Code of Business Conduct and Ethics. The position serves as a resource helping to ensure that the medical device and other regulated operations function within regulatory and relevant standards requirements. This position also ensures all customer requirements are met and that the final product meets all customer requirements.
