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PM Group is currently engaged in the delivery of multiple Life Science projects in the USA. Together we will all be sharing knowledge, learning, growing and continuing to be an integral part of supporting PM Group’s ongoing expansion in the US. You will be executing cutting-edge projects for Cell & Gene Therapy, Biologics, and Pharma facilities – from feasibility through to qualification – for both US and international clients.
$75,000 - $210,000 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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SonoThera technology holds a promise to revolutionize gene therapy by targeting hard to reach organs. “The promise of SonoThera’s technology and approach to gene therapy is inspiring.
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This is a multidisciplinary role & this individual will further interface across many parts of the company to support novel products used in the cell and gene therapy world. We are seeking an innovative and highly motivated individual to join our team as the Manager of Quality Control at our GMP manufacturing facility located in South San Francisco, CA. This position will work with the Quality Control team in supporting our efforts in the GMP manufacturing of cellular therapy products.
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Our client, a leading force in the Cell Therapy space, is committed to providing development and clinical scale services for both gene and non-gene modified cell processing. Recently inaugurated, a cutting-edge cell therapy center now serves as the hub for a broad portfolio of solutions and clinical and commercial services, supporting various partners in achieving their goals.
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We develop, manufacture and sell instruments, biosensors, reagents, and consumables for antibody, gene and cell therapy development. Coordinate sales efforts with Field Application Scientist (FAS) and the Service team for successful product demonstrations, sample workups, and post-sales support.
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GenScript ProBio is the subsidiary of GenScript Biotech Corporation, proactively providing end-to-end CDMO service from drug discovery to commercialization with proactive strategies, professional solutions and efficient processes in cell and gene therapy (CGT), vaccine, biologics discovery and antibody protein drug to accelerate drug development for customers.
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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 Today - 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 Today - 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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Responsibilities Develop bioanalytical assays including analyzing samples from in vivo studies, Developing and validating assays and managing outsourcing activities for biomarker clinical assays gene therapy products.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Plan and execute in vitro safety screens to lead optimize small molecules, ASOs and gene therapy vectors. Experience working across diverse therapeutic modalities, including small molecules, biotherapeutics, nucleic acid therapeutics, and gene therapy is highly desirable.
$265,200 - $439,300 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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As a Senior Director Gene Editing Technologies within the Analytical Development department, you will report to the Vice President Head of Analytical Development and lead a function accountable for establishing deep characterization and knowledge of gene editing technologies used in the manufacture Sana’s cell therapy products.
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In collaboration with UCSF Alpha Clinic and the Living Therapeutics Initiative, the program is committed to driving rapid innovations in academic cell and gene therapy development. In support of cellular and gene therapy programs at UCSF, manage the necessary documentation, submissions, and communications with the FDA for successful IND submissions and in support of clinical studies.
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Based on our innovative approach to developing genetic medicines, as well as our industry-leading internal manufacturing capability and expertise, we have become the Astellas Center of Excellence for their newly created Genetic Regulation Focus Area. We are currently exploring three gene therapy modalities: gene replacement, exon skipping gene therapy, and vectorized RNA knockdown, with plans to expand our focus and geographic reach under Astellas.
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Experience working with or at a cell and gene therapy CDMO for early to pivotal phase products or in a tech transfer role. This will include coordinating with the Analytical Development (AD) team and providing onsite training and assay transfer support at the CDMO for Sana’s cell therapy programs.
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gene therapy jobs in South San Francisco, CA
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