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
Validation Engineer II/III (CSV)
Must have a Bachelors degree in Engineering and 5+ years of validation experience
Manufacturing Supervisor - 2nd Shift (2:00-10:30pm)
Supervise, train, and mentor a team, create a high-performance team, and ensure compliance with cGMPs
Sr. System Administrator
Experience in implementing Controlled Change and Patch Management of GxP systems, system administration, and IT certifications in Linux, Microsoft, or other network-related fields
Lead, QCTS Data Integrity & Computerized Systems
10+ years of experience in IT Systems/CSV, Enterprise Solutions, QMS, and data integrity
Sr./Principal Scientist, Downstream Process Development
2-8 years of relevant industry experience with a solid foundation in biochemical engineering, virology and cell biology, and experience with industry standard chromatography and filtration methods
Validation Technician I/II
AS degree or certificate in a science/technical field, 1+ years of experience in a regulated environment, and excellent communication skills
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
Quality Assurance Document Control & Training Associate
Bachelor's degree, 1-2 years of experience in Document Control or related area, attention to detail and strong communication and customer service approach
Sr/Principal Scientist - Upstream Process Development
MSc or PhD with 6+ years of relevant experience in Bioprocess Engineering/Life Science Biotechnology/Biochemistry/Protein Chemistry, Chemical Engineering or related disciplines, and process development experience
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