Highly motivated, self-starting team player

Ability to prioritize and organize multiple projects in a time-sensitive environment, interact well with all levels within the organization, and communicate well.

This position requires a high school degree and minimum of 3 years experience in a similar regulated environment (cGMP, ISO). Knowledge of Statistical Process Control (SPC) systems and the ability to flowchart/graph data strongly preferred. 

This individual is responsible for inspection of incoming components, in-process product and finished product according to documented specifications, and assists in maintaining the Quality management system in compliance with the current ISO standard and applicable FDA, cGMP regulations.

The position will perform production document review, prepare inspection sheets, and maintain accurate records; troubleshoot quality concerns, prepare shipments including required internal paperwork, pallet shipping documents & labeling, and customer notices. 

ALL INQUIRIES ARE CONFIDENTIAL