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 Sr. Program Manager to support client programs in Process Development and GMP Manufacturing of gene therapy viral vectors. This role involves managing project timelines, client interactions, and ensuring the quality and delivery of products. The Sr. PM will act as the primary point of contact between the client, project team members, and functional groups to track progress and ensure project success.
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.