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Title: Postdoctoral Associate- Alzheimer's Gene Therapy. We are developing gene therapy for Alzheimer's disease targeting the earliest stages of dementia. Discovers, discusses, and deploys new research ideas towards the goal of making gene therapy a reality for neurological disease.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Experience in molecular, cellular, circuit-based, epigenetics or gene therapy approach. The primary purpose of this position is to identify a Addiction Psychiatrist/Physician Scientists with expertise in Psychopharmacology or Non-invasive neural stimulation and a program of research intent on developing reserach grounded in conducting Phase IIB or Phase III randomized clinical trials.
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1+ years of experience within the biotech/biopharma industry in cGMP Operations, preferably within cell and gene therapy. We are seeking an innovative and highly motivated Cell Therapy Manufacturing Associate to join our Process Sciences team who will contribute significantly to the development and manufacture of our advanced cell therapy manufacturing platform.
$20 - $45 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Ongoing projects are related to the identification of solute carriers for small molecule drugs (tyrosine kinase inhibitors, platinum chemotherapeutics, and tubulin poisons) involved in drug uptake into hepatocytes, renal tubular cells, and normal cells affected by therapy; design of preclinical and clinical studies to evaluate pharmaceutical agents as modulators of side effects associated with tubulin poisons.
$48,000 - $55,000 a yearFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Placed in the forefront of our leading- and cutting-edge Cell and Gene Therapy business enabling clients to cure genetic, rare, and otherwise untreatable diseases. At Cell Therapy (CTx) a division of Thermo Fisher Scientific we deliver, from process development through commercial supply, we offer the expertise and resources necessary to help clients deliver innovative gene therapies.
$31 - $42 an hourFull-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Drug Substance or Drug Product manufacturing of advanced therapies (Biotech, Cell and/or Gene Therapy) is preferred. Previous experience directly supporting pharmaceutical operations (e.g., drug substance, parenteral drug product), preference for support with cell or gene therapy.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Experience with early clinical stage cell/gene therapy programs preferred. The ideal candidate brings broad QC experience in early- and late-phase clinical environment, Cell Therapy experience, excellent communication skills, a collaborative can-do mindset, and an agile hands-on approach.
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Experience with cell and/or gene therapy analytical technique (e.g. flow cytometry, qPCR). It is preferable that the candidate have experience working in an aseptic manufacturing facility, preferably in quality assurance, manufacturing compliance, clinical quality, or cell therapy.
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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.
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Our Engenious gene therapy platform is the first to precisely engineer any or all hematopoietic and immune cells with a one-time, off-the-shelf in vivo treatment. We believe the future of medicine lies within us - and this bigger, bolder vision for gene therapy needs incredible people to make it a reality.
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Market knowledge in mAb manufacturing and gene therapy market. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
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We are looking for an enthusiastic, highly organized, and motivated individual who will work on-site within the Gene Therapy Process Development-Process Analytics team at the Burlington, MA, location.
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Strong understanding and knowledge of life sciences markets and processes (fermentation, cell / gene therapy, API, blood products, purification, fill / finish, medical devices, etc) Strong understanding and knowledge of life sciences markets and processes (fermentation, cell / gene therapy, API, blood products, purification, fill / finish, medical devices, etc.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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The Business Development Manager role is designed to establish and grow new partnerships with Cell and Gene Therapy and adjacent Life Science customers by working alongside them at their facilities and identifying potential improvements to ensure regulatory compliance, improve product quality and identify safety and operational efficiency opportunities.
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This position is part of the Cell Culture Product Management team located in Logan, UT, USA, or Marlborough, MA, USA, and will be onsite or hybrid. The Director of Cell Culture Commercial Strategy for Cytiva is responsible for facilitating cell culture innovation initiatives and formulating business strategy while providing insights that enable the leadership team to gain a comprehensive understanding of market trends, growth expectations, competitor intelligence, and voice of our customer.
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