Genezen is a leading gene therapy CDMO founded in 2014, specializing in viral vector production across AAV, lentiviral, retroviral, and other modalities. With state-of-the-art facilities in Lexington and Indianapolis, Genezen offers comprehensive services from process development to cGMP manufacturing, making advanced therapies accessible to both emerging and established companies. Their flexible partnership model and extensive regulatory approvals distinguish them as a trusted provider in the gene therapy industry.
Genezen is seeking a Quality Control Lab Analyst II to support the production and analysis of viral vectors in GMP clinical trials. This role involves independent execution of complex laboratory procedures, sample management, method troubleshooting, and data review. The analyst contributes to method qualification, equipment calibration, and continuous improvement efforts. The position requires adaptability, strong communication skills, and a commitment to high quality standards.
Genezen is a leading gene therapy CDMO founded in 2014, specializing in viral vector production across AAV, lentiviral, retroviral, and other modalities. With state-of-the-art facilities in Lexington and Indianapolis, Genezen offers comprehensive services from process development to cGMP manufacturing, making advanced therapies accessible to both emerging and established companies. Their flexible partnership model and extensive regulatory approvals distinguish them as a trusted provider in the gene therapy industry.
Meridian Bioscience