Sr Technical Writer – onsite

Our client in northern Vermont, a leader in drug manufacturing, has an immediate need for a Sr Technical Writer to work onsite at their facility. This consultant must have experience in a highly regulated environment and ideally has worked in the pharmaceutical industry. Experience with Documentum D2 and Trackwise is highly preferred. Candidates with specific Validation 21CFR Part 11 experience will be given priority. Consultants will work on documentation across several areas including Validation Documents, User Specifications, Requirements Documents and other areas. The consultant will be working under supervision on standardized changes. This work will be focused on getting new equipment into service (writing and executing protocols and CSV documents). They want the person to be on-site as their equipment qualification process generally involves at least some degree of hands-on work with the instruments. This is a 12 month opportunity.