Description
PharmaLogic is hiring an On-Site QA Specialist to support cGMP quality assurance for PET radiopharmaceutical manufacturing. The role oversees materials acceptance and quarantine, batch release and record review, drug quality control, sterility and environmental monitoring, equipment qualification and calibration, investigations, CAPA, SOP maintenance, audit readiness, and ANDA documentation. The position works 10:00 PM to 6:00 AM and may include production, cyclotron, chemistry, and radiation-safety tasks depending on the facility. A relevant BS/BA degree and 1–3 years of pharmaceutical quality experience are required, with pharmacy-tech certification, aseptic-technique, ionizing-radiation, and analytical-equipment experience preferred. Benefits include medical, dental, vision, retirement, disability, life insurance, paid time off, and on-site parking.
