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Extensive management experience in a cGMP testing laboratory environment, with knowledge of regulatory and compendial guidelines as related to cell-based assay requirements, aseptic processing, and biosafety of cell therapy products.
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Empowering researchers to perform single cell sequencing with unprecedented scale and ease, our pioneering approach has enabled groundbreaking discoveries in cancer treatment, tissue repair, stem cell therapy, kidney and liver disease, brain development, and the immune system.
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Preferably one of the following ASQ Certifications: CMQ/OE Certified Manager of Quality/Organizational Excellence, CQA Certified Quality Auditor, CQE Certified Quality Engineer, CRE Certified Reliability Engineer, CSSBB Certified Six Sigma Black Belt. Strong knowledge of regulatory requirements for cell and gene therapy products, ISO-7 cleanroom, and clinical trials is preferred ( eg.
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Arcellx isa public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. Join us in our quest to reimagine cell therapy and destroy cancer.
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Generates and analyzes data to support lab services: ADME Toxicology, Ion Channel, Translational Biology, Cell and Gene Therapy, and Large Molecule Services. Experience in recombinant cell line development, primary cell line isolation, tissue digestion.
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The purpose of the Facility and Reliability Engineer is to development and implement a Reliability Centered Maintenance (RCM) strategy to support client Summit West Cell Therapy Operations and to maintain a qualified and compliant facility operation status.
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The Quality Control Laboratory Manager, Potency Assays will manage quality control testing operations for cell-based potency assays at Iovance’s integrated Cell Therapy Center (iCTC.
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Our faculty and attending physicians provide deep competency across all specialties, including transplantation, stem cell therapy, congenital heart disease, women’s heart health, valve disorders, arrhythmia and hypertension.
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We are seeking a Senior Researcher to join the Department of Bone Marrow Transplant and Cellular Therapy (BMTCT) in our Flow Cytometry and Cell Sorting Core. A reasonable estimate of the current salary range is $60,320 - $105,040 per year for the role of Senior Researcher in Flow Cytometry and Cell Sorting Core.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Thorough working knowledge of in vivo techniques and animal model used in a biopharmaceutical R&D setting, including familiarity with various therapeutic modalities such as small molecule therapeutics, cell therapy, and gene therapy.
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Strong preference for experience within Sickle Cell Disease and autologous cell & gene therapy. Create and conduct Apheresis and Cell therapy lab on-boarding, assessments, training, and collection support and other areas as needed.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Since 1962, the trusted Gibco brand continues to innovate and meet customers' needs in the biotherapeutic, vaccine, biosimilar, cell therapy, and viral vector production markets. Offering the world's largest cell culture media network, we provide services and products for the customer's workflow in both cell culture and cell therapy.
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Daytime, Swing, & overnight openings Overnight pay differential Consistent Hours (no billable hour) Stability and growth opportunities of working with a national agency What were looking for: Bachelors degree; Human Service field degree is preferred (Social Work, Psychology, Sociology, Human Service, Education, Counseling, Family Relations, Nursing, Physical Therapy, Occupational Therapy, Therapeutic Recreation, Speech Language Pathology, Behavioral Sciences, Art Therapy, etc.
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Pursue independent research projects, including the impact of cell based therapy on red cell rheology in SCD, and the effects of vitamin D supplementation on HbF levels and clinical outcomes in SCD.
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The CMC project manager (PM) in Oncology Cell Therapy Tech Ops (CTTO) will build project plans, coordinate delivery of CMC activities in line with project requirements, plan and monitor resources and expenses for product development and clinical manufacture.
$40 - $45 an hourExpandApply NowActive JobUpdated 4 days ago
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