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The successful candidate must have previous experience and be proficient in mouse husbandry, PCR-based genotyping, cell culture, flow cytometry, as well as DNA, RNA, and protein isolation and detection techniques.
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Primary responsibilities that include demonstrating proficiency to perform clinical release testing on cell therapy products, including but not limited to, immunophenotyping (Flow Cytometry), sterility, mycoplasma, viability, residual bead counting, and ex vivo culture assays.
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Experience with bacterial cell culture, molecular or biochemical assays (PCR, ELISA) and protein purification. 1-2 years academic or industrial experience maintaining cell lines and performing mammalian cell culture.
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A demonstrated proficiency in diverse cell biology and biochemistry techniques such as: mammalian cell culture, protein analysis and quantification, microscopy, gene expression analysis, and/or cell-based assays.
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Piper Companies is currently seeking a Sr. Regulatory Operations Specialist to support a growing and innovative cell and gene therapy company in Philadelphia, PA (Hybrid Schedule). Keywords: Regulatory, IND, CTA, SharePoint, Gene Therapy, Cell Therapy, Biotechnology, FDA, Pharmaceutical, Regulatory Submission.
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Tower climber, tower foreman, telecommunications, cell tower te. tower climber, tower foreman, telecommunications, cell tower te. The Tower Technician will be responsible for the performance of various construction tasks in the areas of tower erection, coaxial cable and antenna installation, antenna mount installation, RF testing and troubleshooting.
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The ideal candidate will have experience in cell culture and multicolor flow cytometry. Good understanding of cell culture and aseptic technique. Experience with cell culture (primary cells and immortalized tumor cells.
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Additional responsibilities are installation and maintenance of wireless radio communications systems including radio propagation modeling and prediction, microwave path analysis, interference analysis, frequency coordination, cell site equipment layout, parameter definition, and ancillary equipment.
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Experience with cell culture, aseptic technique, cell-based potency assays, and flow cytometry. 3+ years of experience in the pharmaceutical industry within a GMP Quality Control role; experience with cell therapy products is a plus.
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Tissue culture of a variety of mammalian cell types, especially iPSCs. Prior experience in any of the following is preferred: molecular cloning, DNA sequencing, PCR, Western analysis, flow cytometry, and cell based assays.
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Skills & Abilities: Extensive scientific HLA knowledge and technical skills in the following areas preferred: HLA serology and molecular genetics, HLA antibody screening /identification of HLA antibody specificity, cross matching techniques to support stem cell transplantation programs and platelet transfusion therapy and other areas in the field of Histocompatibility and Immunogenetics.
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Detail-oriented with expertise in FDA submission requirements and familiarity with cell and gene therapy regulatory standards in major markets like the US and EU. Compensation & Benefits for the Sr. Regulatory Operations Specialist.
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Scientists performing stem cell, immunology, cancer, regenerative medicine and cellular therapy research are among those who rely on our cell culture media, cell separation products, instruments, ancillary reagents and contract assay services.
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5+ years of hands-on Quality Systems experience working within a Cell and Gene Therapy or Biologics manufacturing environment. You'll be responsible for providing Quality Systems oversight and support for the development and operations of a commercial scale state-of-the-art cGMP cell therapy manufacturing and laboratory facilities.
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Cabaletta Bio (Nasdaq: CABA) is a clinical-stage biotechnology company focused on the discovery and development of engineered T cell therapies that have the potential to provide a deep and durable, perhaps curative, treatment for patients with autoimmune diseases.
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bioengineering cell culture jobs in Philadelphia, PA
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