Description
The vendor or client is seeking a Quality Validation Engineer with at least six years of experience in pharmaceutical or biopharmaceutical manufacturing. The role requires strong expertise in quality validation, quality systems, regulatory compliance, CAPA, QSR, FDA, and GMP requirements. Responsibilities include supporting equipment, process, facility, computerized systems, and validation documentation activities, as well as reviewing documentation for GMP and regulatory compliance. A bachelor's degree in Electrical Engineering or a related engineering field is required, while a master's degree is preferred.
