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Join FDB and help create the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. Degree in Biology, Microbiology, Chemistry, Biochemistry, Engineering or related field.
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Partnering with AmplifyBio for manufacturing cell therapy, gene therapy, mRNA, plasmid, or other modality is quite different from a typical CDMO experience. with a track record of success in GMP environments who understands biologics processes (i.e., cell & gene therapy, aseptic environments, reagent control, contamination control.
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Minimum of 12 years of related experience with a Bachelor’s degree, 8 years and a Master’s degree, or a PhD with 5 years experience, or equivalent experience, with at least 3 years of experience directly in the cell and gene therapy field; degree in Chemical or Biological Engineering, Molecular Biology, Genetics, Virology, or related disciplines.
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Within Ginkgo, the Mammalian Engineering team consists of a set of scientists and engineers with subject matter expertise across cell therapy, gene therapy, rna therapeutics, and biologics.
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Understanding of molecular biology techniques related to gene therapy. The Associate Director, Regulatory Affairs will establish and grow internal CMC regulatory activities, providing strategic management and content plans to support Vyriads gene therapy product development, registration, and post-approval strategies.
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The position will be responsible for crafting and assuring development and execution of regulatory strategies for biological drug products and combination products globally, providing direction on the interpretation and application of global CMC regulations and guidance related to gene therapy.
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5+ years of hands-on Quality Systems experience working within a Cell and Gene Therapy or Biologics manufacturing environment. This is an exciting opportunity to lead GxP Quality Systems within a promising Cell & Gene Therapy company revolutionizing cancer immunotherapies.
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Voyager’s TRACER™ AAV capsid discovery platform has generated novel capsids with high target delivery and blood-brain barrier penetration at low doses, potentially addressing the narrow therapeutic window associated with conventional gene therapy delivery vectors.
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GenScript's businesses encompass four major categories based on its leading gene synthesis technology, including operation as a Life Science CRO, enzyme and synthetic biology products, biologics development and manufacturing, and cell therapy.
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Gene editing and cell therapy are dramatically changing how we treat cancer and other major illnesses. Crop science and synthetic biology are producing sustainable and ethical food.
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Calibr-Skaggs is seeking a talented Research Scientist in gene and cell therapy/immuno-oncology to join our effort to create a transformational gene and cellular therapy approach.
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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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In this role, you'll be a key player in developing high-impact marketing assets and web content that effectively communicate our brand message and propel our commercial success in the Cell & Gene Therapy market.
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3) Experience in the areas of gene therapy, drug delivery, cellular/molecular biology, mechanical/bioengineering highly preferred. 3) Experience in the areas of gene therapy, drug delivery, cellular/molecular biology, mechanical/bioengineering highly preferred.
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In-depth knowledge of immunology, particularly in cancer biology and T-cell therapy. Global Life Science Hub is proud to partner with a cutting-edge biotech company dedicated to revolutionizing cancer treatment through innovative gene therapy modalities.
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