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5+ years of Specialty Sales experience in Pharmaceutical, Biopharmaceutical, Biologics or Medical Device sales experience. Infusion/rare disease sales experience in both the Outpatient Infusion setting and Specialty Pharmacy channel with a strong understanding of pricing and reimbursement.
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For more than 70 years, we have been at the forefront of neuroscience research. Lundbeck is a global pharmaceutical company specialized in brain diseases. Our research programs tackle some of the most complex challenges in neuroscience, and our pipeline is focused on bringing forward transformative treatments for brain diseases for which there are few, if any therapeutic options.
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10+ years of experience implementing biosafety and EHS programs: biosafety, biologics manufacturing, hazardous waste determination and management, occupational health, IH, environmental permitting, DEP, DOT, and OSHA.
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BRC builds the biologics pipeline in collaboration with Novartis Biomedical Research (NBR) Disease Areas and Platforms via a breadth of technologies for discovery of antibody, protein, gene therapy and RNbased therapeutics.
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You are a dynamic Computational Scientist who will work with other scientists to apply cutting-edge computation, Machine LearningDeep Learning approaches to revolutionize our large molecule computational tools by contributing to accelerating and improving the process of design and engineering of novel biologics drug candidates.
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Territory boundaries include: Southern Chicago, Tinley Park, Downers Grove, Bensenville, IL & La Porte, Valparaiso, Merrillville, Michigan City and Remington, IN. Are you a results-driven pharmaceutical sales professional looking to be part of a collaborative, agile and patient-focused organization.
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5+ years’ experience in GMP Quality or Manufacturing in biopharma/biologics/pharma industry. We are looking for a Manager/Senior Manager of Quality Operations to help provide quality oversight for our biologics commercial and clinical development programs.
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Experienced Senior Process Development Associate will be responsible for independently executing bench-scale experiments to develop, characterize, and optimize manufacturing processes involving production of protein biologics and plasmid DNA. The Senior Associate will work with scientists, engineers, operators, and other associated groups to optimize, implement, and tech transfer new processes and to troubleshoot any process-related problems.
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Biologics Process R&D Senior Scientist page is loaded. Biologics Process R&D Senior Scientist. Beyond process development for pipeline biologics, we innovate and build next generation biomanufacturing technologies.
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Biologics process development experience, particularly designing and scaling up of bioreactor and purification processes for protein therapeutics. Process Engineering also partners with Biologics CMC Development and Aesthetics R&D functions to provide active engineering support to enable robust process scale-up and manufacturing of biologics drug substances and drug products including toxins and cosmetic active ingredients (CAIs.
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The latter two together form our Biologics' Process Development (BPD) group. Work with a collaborative, cross-functional team of talented scientists and engineers to advance the biologics pipeline from early- to late-stage development.
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Successful candidates will have a familiarity with upstream and downstream biologics manufacturing, tissue culture, column chromatography and other purification processes. Must have experience in mammalian cell culture, tangential flow filtration, and/or column chromatography required Experience in biologics manufacturing preferred.
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SummaryThe Veterinary Biologics Science and Policy Advisor is in the Office of the Director, Center for Veterinary Biologics (CVB), and provides policy and scientific advice in planning, organizing, and evaluating broad biologics programs, particularly involving tools and systems for the prevention, detection, treatment, and control of diseases which threaten the nation's livestock resources.
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We are global leaders in providing products and services within the fields of nucleic acid production and biologics safety testing to many of the world's leading biopharma, vaccine, diagnostics, and cell and gene therapy companies.
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The U.S. Pharmacopeial Convention (USP) USP is an independent scientific organization that collaborates with the world's top experts in health and science to develop quality standards for medicines, dietary supplements, and food ingredients.
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