Description
Quality Consulting Group is hiring a manufacturing quality specialist to support pharmaceutical, biotechnology, medical device, and manufacturing operations in Puerto Rico and the United States. The role owns change controls, process validation, CAPA investigations, risk assessments, training, commercial campaign readiness, functional and water testing, MBR creation, and manufacturing procedures, while also serving as a peer-recognized specialist in at least one technical area. Candidates need a bachelor's degree in a relevant scientific discipline, cGMP industry experience, change-control and quality-systems expertise, TrackWise and SAP proficiency, and strong analytical, communication, and cross-functional collaboration skills.
