Description
PharmaLogic is hiring a full-time, on-site Site Quality Assurance Manager to oversee cGMP quality assurance for PET radiopharmaceutical manufacturing. The role covers materials acceptance and quarantine, batch release and record review, drug quality control, sterility and environmental monitoring, equipment qualification and calibration, investigations, CAPA, SOP maintenance, training, audit readiness, and FDA and agency inspection support. The position reports to the PET Facility Manager and requires a relevant BS/BA degree, 3–5 years of pharmaceutical quality experience, and knowledge of cGMP and radiation safety; benefits include medical, dental, vision, retirement, disability, life insurance, paid time off, and on-site parking.
