Description
Quality Consulting Group is seeking a Specialist Manufacturing for a contracted biopharmaceutical role in Juncos, Puerto Rico. The position focuses on supporting manufacturing and quality systems in a GMP environment, including non-conformances, process validation, procedures, training, new product introductions, investigations, CAPAs, change control, and continuous improvement. Candidates need a bachelor's degree in life sciences, biology, chemistry, or engineering, plus experience in biotechnology/pharmaceutical process support, knowledge of systems such as SAP, TrackWise, PAS/X electronic batch records, and Veeva, and the ability to work with cross-functional teams on administrative shift.
