Other: Scientist IV/V, Analytical Chemistry - Rockville, Maryland - (Rockville, MD)

This is a non-supervisory scientific position in the Chemical Medicines Department (CM) reporting to Director/Team Leader. The role is that of an individual contributor. The incumbent is responsible for the development of monographs for small molecular-weight pharmaceuticals (drug substances and associated dosage forms) in the USP-NF and supports USP Expert Committees and associated Expert Panels. The department works closely with Reference Standards Evaluation (RSE) Compendial Development Laboratories (valid drivers license) within Global Laboratory Organization (GLO) and other departments such as Publications (PUBS), Executive Secretariat and Compendial Affairs. Roles and Responsibilities: Develops new monographs and revises existing monographs based on supporting data submitted by USP global laboratories and external sponsors Evaluates analytical methodology and acceptance criteria Redesigns existing official monographs Works closely with a team of high-performing scientists responsible for the development