Description
The Document Control Administrator manages the medical device document lifecycle, including document creation, revision, version control, compliance with FDA 21 CFR Part 820 and ISO 13485, SAP and database maintenance, change management, audits, reporting, training, and process optimization. The role requires at least one year of similar experience, knowledge of Microsoft Office and computer skills, and a high school diploma or GED; SAP, regulated-industry documentation, C2C administration, and Visio experience are preferred. The position is based in Canaan, Connecticut, on the first shift from 8:00 a.m. to 4:30 p.m.
