first draft needs to be written by first week of December and final draft needs to be completed by the end of December.
Our client has 50% of the site master file written for the cell and gene therapy manufacturing facility. The site master file contains all of the information about the manufacturing facility that would go into a regulatory filling such has the quality systems that are in place, information regarding the clean rooms, products they manufacture, WIFI utilities and controls in place, etc etc. Our client is looking for a candidate who has written at least 2-3 site master files for biologics manufacturing facilities to bring this to completion.
Remote: Site Master File Author (232043)