Description
The role manages, maintains, monitors, standardizes, and categorizes documents in a document management system; develops templates; structures documents; and serves as the primary contact for document-related questions and internal documentation requirements. It requires a degree or training in Chemistry, Pharmacy, or a related natural science field, pharmaceutical CMC experience focused on pharmaceutical development analytics, strong communication and organizational skills, and English proficiency. GMP and Veeva OneVault experience are desirable. Benefits include 30 days of vacation.
