Gene therapy CDMO specializing in viral vector manufacturing at scale
Genezen manufactures viral vectors (AAV, lentiviral, retroviral) for gene and cell therapy developers. The hiring mix—skewed toward engineering, quality, and manufacturing roles with accelerating velocity—reflects active scaling across production platforms. Current projects span downstream processing (50L systems), analytical method development and tech transfer, and LIMS/ELN implementation, signaling infrastructure build-out to support gmp scale-up and process robustness as they move programs toward pivotal trials.
Genezen is a contract development and manufacturing organization (CDMO) for viral vectors used in gene and cell therapies. Founded in 2014, the company operates two manufacturing sites—one in Lexington, Massachusetts (holding FDA, EMA, Health Canada, and MFDS Korea licenses and currently producing a commercial viral vector product) and one in Indianapolis, Indiana (supporting cGMP manufacturing for a program entering pivotal clinical trials). Genezen serves innovator organizations across all stage and size, from early-stage to established companies, and maintains a technical stack anchored in analytical instrumentation (HPLC, qPCR, ddPCR, SDS-PAGE, LIMS, Veeva) alongside traditional lab and manufacturing systems.
Genezen manufactures viral vectors including AAV, lentiviral, and retroviral modalities for gene and cell therapy applications. The company holds regulatory licenses from the FDA, EMA, Health Canada, and MFDS Korea and operates cGMP manufacturing facilities.
Genezen operates two sites: Lexington, Massachusetts (holding multiple global regulatory licenses and producing commercial viral vector products) and Indianapolis, Indiana (supporting cGMP manufacturing for programs entering pivotal clinical trials).
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