Teams at Oakworks, Inc.

Inspect received, in-process, and finished medical/spa equipment; document quality records; identify and disposition nonconforming material; facilitate calibration; prepare management reports; train employees on quality procedures and defect recognition, including welding inspection; assist with supplier and production quality tracking.

Hands-on role owning regulatory requirements and document control for medical devices. Maintain QMS compliance (FDA 21CFR 820, ISO 13485, ISO 14971), perform trending analysis, manage quality projects, and use quality system software (QT9 preferred).