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Summary
About the Role
About You
- BS, MS, or PhD in biological engineering.
- 5-8 years of relevant industry experience.
- Knowledge of chromatography with AKTA system and Unicorn software.
- Experience with TFF, aseptic technique, and cGMPs.
- Ability to interface with multi-disciplined teams.
- Experience in process optimization and compliance with OSHA, EHS, and Quality procedures.
Benefits
- Paid vacation, sick time, and holidays.
- 401(k) with match.
- Healthcare plans including dental & vision.
- Life and accident insurance.
- Disability options.
Founded in 2014 in Indianapolis, IN, Genezen is a best-in-class gene therapy CDMO with over a decade of experience supporting the cell and gene therapy manufacturing market worldwide. With capabilities across vector-modalities (AAV, lentiviral, retroviral, and others), Genezen partners with innovator organizations to deliver potentially life-saving gene and cell therapies – from concept to commercial. With flexible and customer-centric programs, Genezen tailors its partnership-model approach to all sizes and stages of organizations, to make viral vector production accessible to both early-stage, growth-oriented companies and established industry leaders. Genezen’s state-of-the art Lexington, MA site holds multiple global regulatory licenses, including with the FDA, EMA, Health Canada, and MFDS Korea, in support of the active manufacture of a commercial viral vector-based product. Our Indianapolis, IN site provides cGMP manufacturing for viral vectors and is currently supporting a program entering a pivotal clinical trial.