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Hands on proficiency and with protein analysis using HPLC, CE-SDS, Western blotting, Spectroscopy, etc. , CE-SDS, PicoGreen, Capillary Western(Jess), A280, mass spectrometry, etc.
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E.g., HPLC, FPLC, Western Blot, SDS-PAGE, Protein Simple Wes and other analytical tools. Responsible for day to day running of experiments and data analysis in the protein chemistry laboratory.
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3-5 years of analytical experience in protein/peptide separations by CE-SDS and/or cIEF in pharmaceutical or biotechnology companyScientific and practical knowledge of protein characterization for protein therapeutics including monoclonal antibodies and glycoproteinsAbility to take initiative in problem solving and consistently bring independent, scientific approach to method developmentThe duties of this role are generally conducted in an lab environment.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Proficiency running analytical methods a plus; such methods may include SDS-PAGE, Endosafe, UV spectroscopy, and HPLC. Strong protein purification knowledge and experience, including familiarity with AKTA Pilot (or Avant) chromatography systems and UNICORN software.
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Knowledge of a variety of analytical techniques including SEC, AEX, RP-HPLC, CE-SDS, icIEF, ELISA, GC, and mass spectroscopy. The position is responsible for analytical development, analytical technology transfer and validation, and overall management of CMC activities related to external QC testing/release and stability of antibody drug conjugates and intermediates.
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Working closely with protein biochemist: Assess protein inventory, check the quality of our proteins in activity assays, characterize purity and post-translational modification using different techniques (Western Blot, SDS-PAGE, Size-Exclusion Chromatography, HPLC); optimize buffer and additive conditions for protein screening by thermal stability (nanoDSF, TSA.
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Lead analytical development activities for the characterization of antibodies and/or synthetic peptides utilizing HPLC, LC-MS, Capillary Electrophoresis, peptide mapping, Mass Spectrometry, SDS-PAGE, ELISA, gel electrophoresis and modern glycoprotein & carbohydrate characterization techniques.
$166,700 - $241,325 a yearFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Antibody characterization/QC by SDS-PAGE, HPLC-SEC, and Gator to determine antibody quantity and quality. Support antibody expression construct generation by molecular cloning, DNA sequencing, and plasmid DNA purification.
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A strong background in protein chemistry will be essential to perform and troubleshoot techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays.
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The person will be responsible labeling of reagents (protein and antibodies), purification and characterization including concentration estimation, SDS-PAGE, SE-HPLC, endotoxin estimations etc.
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HPLC, ELISA, SDS-Page, Gel Electrophoresis experience preferred. Catalent Biologics is a fast growing business within Catalent Pharma Solutions focused on providing innovative technologies and solutions to help more and better biologic treatments get to patients.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Demonstrated success working with techniques such as HPLC, SDS-PAGE, cell-based bioassays, capillary electrophoresis, SDS-PAGE, ELISA, and standard compendial assays. One block east of the Chicago White Sox Stadium.
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Hands-on experience with at least two techniques, such as HPLC, capillary electrophoresis, ELISA, or SDS-PAGE, used for analysis of recombinant proteins. QC Analyst 2 will contribute to the success of the operation by providing accurate, GxP-compliant analyses of clinical biopharmaceutical products and by participating in assay qualification and validation studies.
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At least 2-4 yrs working experience in a cGMP Quality Control, analytical development, analytical transfer or validation department in a FDregulated industry. The individual will contribute to the success of the operation by providing accurate, GxP-compliant analyses of clinical Biopharmaceutical products and by participating in assay qualification and validation studies.
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Hands on experience with downstream analysis techniques including, but not limited to, HPLC, SDS-PAGE, Western Blots, ELISA, and ddPCR. Knowledge and experience with large scale protein purification, nucleic acid purification, and other chromatography application processes.
Full-timeExpandApply NowActive JobUpdated 17 days ago
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