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We work closely on Prevail s Adeno-Associated Virus (AAV)-based gene therapy programs to progress our mission of curing disease. We are seeking a motivated research associate who can take on ownership of established molecular biology assays as well as contribute to the development of new cutting-edge assays for testing AAVs. Responsibilities: Contribute to all aspects of analytical assay development, from design to qualification, for our AAV-based drugs.
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In this role, the Molecular Biology Quality Control Analyst I will be responsible for supporting the gene therapy program pipeline, including but not limited to routine GMP testing of AAV vector analytical methods such as GC titer determination by ddPCR and qPCR, impurity testing, and other methods as needed.
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Requirements: Ph. D., M.S., or B.S. degree in the life sciences from a four-year college or university and a minimum of 5 years of sales and sales management experience within the life sciences industry (prefer cell and gene therapy); or equivalent combination of education and experience.
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BlueRock Therapeutics, a wholly-owned and independently operated subsidiary of Bayer AG, is a leading engineered cell therapy company using its unique cell+gene platform to direct cellular differentiation and genetically engineer cells to create a new generation of cellular medicines that address large patient populations suffering from neurological, cardiovascular, and immunology diseases.
$120,000 - $125,000Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Experience with next generation sequencing (WGS, RNAseq, ChIP-seq), gene editing (CRISPR), and/or mouse cancer models (transgenic or xenograft models) are also desired. The candidate will lead the development and evaluation of cell therapy-based approaches with the goal of translating promising constructs into the clinic for the treatment of pediatric cancer.
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By bringing extensive knowledge of the vaccines, cell and gene therapy and biologics market in especially the fill and finish and drug product manufacturing area the candidate will contribute to the business growth.
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In depth knowledge of biologics, including vaccines, protein, cell and gene therapy, and their manufacturing and quality controls. Clean Biologics is an expert in quality control of Biologics, manufacturing of starting materials (Cells Banks & Virus banks), storage of biologics as well as development and validation of customized Bioassay.
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These include, but are not limited to, the FDA (Food and Drug Administration), state departments of health, state laboratories, blood and tissue regulators, Foundation for the Accreditation of Cellular Therapy (FACT) and CMS (Center for Medicare and Medicaid Services) / CLIA (Clinical Laboratory Improvement Act.
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Our studies encompass a wide variety of techniques, including mammalian cell culture, transfections, lentiviral/retroviral infection, western blotting, immunoprecipitation, RT-qPCR, ChlP-qPCR, immunostaining, and gene therapy using animal models of PAH. Apply today.
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BS/BA degree in Business, Science, Engineering or related field with 15+ years of experience in global supply chain from pharma, (preferably) biotech or cell & gene therapy companies. BS/BA degree in Business, Science, Engineering or related field with 15+ years of experience in global supply chain from pharma, (preferably) biotech or cell & gene therapy companies.
Full-timeRemoteExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Application specific knowledge of the biologics and gene therapy market would be highly beneficial but not essential. Experience in the biologics and gene therapy markets preferred.
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We provide biomanufacturing strategy and execution to start up and established gene and cell therapy, pharmaceutical, and biotechnology companies. Project Farma (PF) is the leading advanced therapy technical operations consulting company in the life science industry.
$96,000 - $135,000 a yearExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Deep understanding of upstream and downstream processing, cell and gene therapy manufacturing principles, and regulatory requirements. Strategic thinker with a vision to drive innovation and push the boundaries of technology in the RNA gene therapy space.
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Project Farma is a wholly owned subsidiary of Precision Medicine Group, LLC, a leading global life sciences company with over 2,000 employees. Precision Medicine Group is an Equal Opportunity Employer.
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Gene Therapy experience in a biotech company preferred. Liaise with Chief Scientific Officer and CSO Team regarding preclinical and nonclinical activities relevant to corporate pipeline and clinical development strategy.
$175Full-timeExpandApply NowActive JobUpdated 3 days ago
gene therapy jobs in New York, NY
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