About The Role

The Quality Inspector I is responsible for performing inspections and quality assurance activities to ensure that raw materials, in-process components, and finished medical device products meet established specifications and regulatory requirements. This role supports compliance with FDA Quality Management System Regulations (QMSR), 21 CFR Part 820, ISO 13485, and company quality standards by executing inspection protocols, documenting results, and identifying nonconformances within the production area.

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