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.
Open Positions
Manufacturing Technician II/III
Requires Associate or BS degree in Biology, Biochemistry, Molecular Biology, or similar field. 1-5 years of relevant cleanroom GMP industry experience
Lead, Quality Systems
5+ years of experience in Quality Assurance or Quality Systems, Bachelor's degree in a related field, experience with Veeva and/or other eQMS software systems
Sr. Engineer, Manufacturing Sciences & Technology
Bachelor's degree in engineering or related field. 6+ years’ experience, or equivalent MS degree. GMP experience and strong data analysis/statistical skills are crucial
Sr. Associate, Quality Operations
Bachelor's degree, 6+ years of experience in Quality Assurance, leadership responsibilities
Scientist II, Upstream Process Development
The ideal candidate will have a BS or MS in biochemistry, chemical engineering, and 4-8+ years of relevant industry experience
Scientist I, Analytical Development
BS in science/technical field. 2-4 years' experience in method development and cGMP compliance. Proficiency in HPLC-based methodologies and electronic lab notebook documentation
Sr. Program Manager
BS in scientific field preferred. 5+ years of experience in pharmaceutical/biotech roles. 3+ years of life science laboratory experience
QC Scientist - Critical Reagents
BS/MS in Life Sci/Eng. 8+ yrs pharma/biotech exp. Extensive knowledge of cGMP/ICH/FDA guidelines, references standards programs & biostatistics. Strong analytical and communication skills
Quality Control Lab Analyst II
Associate/BS degree in relevant field. 2+ years of QC/R&D/operations experience. Excellent communication skills are required
Scientist I/II, Downstream Process Development
BS in biological engineering, 2-8 years of industry experience, and solid foundation in biochemical engineering, virology, and cell biology
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