Susan Schniepp has been appointed vice president of quality at OSO BioPharmaceuticals Manufacturing. Ms. Schniepp will manage all operational quality-related issues and is responsible for cGMP compliance of OsoBio’s facility, including validation, regulatory affairs, and records and filings. Ms. Schniepp has more than 30 years of professional experience managing quality assurance within the pharmaceutical industry. Recently, she served as chairwoman of the Monograph Development–Psychiatrics...