Description
Leading the change order process including engineering change orders, manufacturing change orders, deviations and engineering change requests* Review the changes to verify they are completed meeting the requirements to procedures
* Identify change order improvements, drive improvements to completion including documentation development, training and implementation
* Lead Engineering/Quality Engineering with Verification and Validation Protocol and Report requirements
* Write, execute and edit test plans
* Troubleshoot items as needed
* Lead project teams in building out Project deliverables (Design History File and Device Master Record)
* Lead CAPA systems activities and support internal and external audits performed internally or by the FDA and additional external parties
* Monitor and prioritize business need in order to complete and close all activities in a timely manner
To find out more about Real please visit www.realstaffing.com