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
Director of Business Development
5+ years of sales/technical experience or client relationship experience, ideally in a bio-manufacturing or CDMO environment, with a strong understanding of gene therapy and gene modified cell therapies
Stability Manager, Quality Control
8+ years of industry experience in CDMO, Master's Degree in science-related field, experience managing stability programs for cell/gene therapy products
Manufacturing Supervisor - 2nd Shift (2:00-10:30pm)
Supervise, train, and mentor a team, create a high-performance team, and ensure compliance with cGMPs
Manufacturing Supervisor - 1st Shift
5-7 years of cGMP experience, Bachelor's Degree in Life Sciences/Engineering, detail-oriented, process-oriented way of thinking and working, and able to communicate professionally on diverse levels and channels
Manufacturing Technician I/II/III (2nd Shift)
High school diploma and 2-4 years related cGMP industry experience or an Associate’s Degree in Life Sciences/Engineering field with 1 year of cGMP Manufacturing experience or Bachelor’s degree in life Sciences/Engineering field
Validation Engineer II/III (CSV)
Must have a Bachelors degree in Engineering and 5+ years of validation experience
Specialist I/II/III, Calibration
3-5 years related Calibration/Metrology work experience, Associates Degree or Bachelor's degree, ability to understand user manuals/specifications, wiring diagrams, equipment Piping & Instrumentation Diagrams (P&ID), and Standard Operating Procedures (SOP)
Sr. Program Manager
BS in scientific field preferred. 5+ years of experience in pharmaceutical/biotech roles. 3+ years of life science laboratory experience
Lead, QCTS Data Integrity & Computerized Systems
10+ years of experience in IT Systems/CSV, Enterprise Solutions, QMS, and data integrity
Automation Engineer I/II/III
B.S in Engineering, Computer Science, or related field. 2-8+ years relevant experience. Familiarity with cGMP operations and 21 CFR Part 11 regulations
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