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Sourcing Strategy Development - Co-develop and implement sourcing strategies with the business unit to enable development and commercialization of cell and gene therapy products.
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The ElevateBio ecosystem combines multiple R&D technology platforms – including Life Edit, a next-generation, full-spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non-viral therapeutic delivery platform – with BaseCamp, its end-to-end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics.
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Job DescriptionDirector, R&D Quality, GCP - Cell Gene Therapy (CGT)The Director of R&D Quality, GCP - Cell Gene Therapy (CGT) reports directly to the Head of RDQA and is a trusted advisor and partner to clinical and quality stakeholders and business partners and supports the program and study level quality leads in key quality related clinical activities and deliverables for all CGT programs across the Vertex clinical portfolio.
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You will be working with the Cell Therapy Process Development team and will be a qualified DD&T leader to drive CMC digitalization technologies and endpoints across Takeda pipeline and platform activities.
$209,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Director of R&D Quality, GCP - Cell Gene Therapy (CGT) reports directly to the Head of RDQA and is a trusted advisor and partner to clinical and quality stakeholders and business partners and supports the program and study level quality leads in key quality related clinical activities and deliverables for all CGT programs across the Vertex clinical portfolio.
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Our clinical research and development team is dedicated to tailoring cell and gene therapies to individual patients, specifically working on treatments for hematological cancers using chimeric antigen receptor (CAR) T cell technology.
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The incumbent will supervise routine cGMP manufacture of multiple cell and gene therapy types/products at our state-of-the-art BaseCamp facility such as autologous/allogenic cell therapies and other advance therapies including mRNA and/or Lentiviral Vector (LLV.
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This client is a growing international full-service CDMO/CRO within the biotechnology space looking to aggressively expand its footprint in the US. The company has a strong base of API/Small Molecule, Biologics, Clinical Research, Bioanalytical Sciences, DMPK, Cell and Gene Therapy and other capability centers across the US. This business has developed a fantastic brand in the US through exceptional service which drives repeat business.
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The Manager of Strategic Communications & Thought Leadership is a dynamic role designed to enhance both internal and external communication efforts within the Cell Culture Cell Therapy business.
$130,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Providing advice on regulatory issues for both marketed and pipeline products; actively collaborates with management, Global Regulatory Lead and cross functional colleagues within Alexion (i.e., commercial, research, clinical development, medical affairs, business development, legal, manufacturing, quality, portfolio management, financial, human resources, etc.
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These facilities encompass Product Analysis and Development, Cell Therapy Analytical, and Nucleic Acid Process Development laboratories, and will also support future state GMP Operations in Cell Therapy.
$180,000 a yearFull-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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This role involves identifying new business opportunities, forging strategic partnerships, and expanding our client base in the gene therapy manufacturing sector on the east coast. Understanding of cell and gene therapy research.
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Lead development and execution of the commercial and business strategy in the Cell Therapy Franchise. Acts as day to day commercial and business escalation for Cell Therapy within RESILIENCE, serves active role in governance of customer relationships and site on respective PAD and manufacturing SLT (s.
$235,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Extensive experience in the medical/regulatory writing field gained in a pharmaceutical/biotech industry or Contract Research Organisation environment, particularly in Immunology Cell Therapy.
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In depth knowledge of biologics, including vaccines, protein, cell and gene therapy, and their manufacturing and quality controls. This position is a Business Development role within the newly formed and growing BD Lab under Archimed, focusing on driving business in the US market for our portfolio company, Clean Biologics.
$150,000 a yearFull-timeExpandApply NowActive JobUpdated 1 month ago
business development cell therapy jobs in Cambridge, MA
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