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Comprehensive knowledge and understanding of protein/peptide chemistry, protein chemical and physical stability, folding, and structure-activity relationship. Principal Scientist Level: Ph. D. with 5+ years of experience or MS with 6-9 years of experience with degree in Pharmaceutics, Biochemistry, Chemistry, Pharmaceutical Chemistry, Molecular Biology, Bioengineering, Chemical Engineering or related disciplines.
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In-depth knowledge of analytical chemistry, with hands-on experience in chromatography techniques (HPLC, UPLC, 2D-LC) or electrophoretic techniques (CE-SDS, CZE, icIEF) for protein and nucleic acid analyses.
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BMS is looking for a Principal Scientist with a desire to contribute in the fast-paced early development matrix environment by supporting pre-formulation, physico-chemical characterization, and formulation development of oral and parenteral dosage forms for new drug candidates in support of preclinical and clinical studies.
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Established leadership skills, including management of individuals and teams working towards common clinical/scientific goalsConsistent track record of managing timelines and driving key results in a matrixed organizationExcellent communication, interpersonal, and written skillsPreferred Qualifications:R&D experience at a pharmaceutical company, biotech or partner organizationFamiliarity with drug discovery and clinical development processes.
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And minimum 7 years global Drug Safety/Pharmacovigilance clinical trial and post marketing experience in a pharmaceutical or biotechnology industry in positions of increasing technical and leadership responsibility.
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The successful candidate excels in a collaborative, cross-functional, matrix team environment to enable the development of new drug products for pharmaceutics, biologics, and emerging modalities such as, but not limited to, antibody-drug conjugates, gene therapy, oligonucleotides, and SiRNA nanoparticulate delivery.
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Ph. D. in engineering, pharmaceutical science, chemistry, biochemistry, physics or other quantitative area of study with 0-3 years of experience; M.S in engineering, pharmaceutical science, chemistry, biochemistry, physics or other quantitative area of study with 3-5 years of experience; or B.S. in engineering, pharmaceutical science, chemistry, biochemistry, physics or other quantitative area of study with more than 5 years of experience.
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The lab is hosted in the Institute for Quantitative Biomedicine, co-located with the RCSB Protein Data Bank. In addition to the Rutgers Cryo-electron Microscopy and Nanoimaging Facility, core facilities housed within the Institute include protein NMR spectroscopy, mass spectrometry, and hardware for high-performance computing.
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What differentiates Lilly IT is that we create new possibilities through tech to advance our purpose - creating medicines that make life better for people around the world, like data driven drug discovery and connected clinical trials.
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Data Management and Analytics: Oversee the collection, integration, and analysis of large-scale scientific data sets, from the lab to the trials, utilizing advanced analytics and machine learning to extract valuable insights for drug discovery and development.
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Qualifications:PhD or MS in Analytical Chemistry, Chemistry, Biochemistry, or another relevant field. Overview Within the Translational Bioanalytical Sciences (TBS) group of Clinical Development, the role focuses on LC-MS/MS of small and large molecule quantitative assay development of biological samples.
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Knowledge of quality control lab activities and procedures, technical knowledge of Analytical Chemistry. Or a doctorate from an accredited four-year college or University in chemistry, biochemistry, or a related scientific field with a preferred 1- 3 years of experience working in a laboratory in a manufacturing or academic setting.
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Biotechnology, biological science, sterile environment, sample collection, Histology, Pathology, Ascp, Immunohistochemistry, Tissue samples, Chemistry, Biology, biochemistry, Staining, Accessioning, Specimen processing, Sample preparation, embedding, sectioning.
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Lilly’s Purpose At Lilly, we unite caring with discovery to make life better for people around the world. Demonstrable experience in tools / platforms such as MES Syncade and Integration technologies enabling data flow with downstream systems (e.g. OSI PI, Data Lakes, Process Monitoring systems such as JMP, Tableau, Power BI)Your Basic Qualifications: Bachelor’s degree in Software Engineering, Computer Science, Computer Engineering, or a related field.
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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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protein chemistry drug discovery jobs in Somerset, NJ
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