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A proven track record of 2-4 years of relevant experience selling a portfolio of contract manufacturing services including upstream and downstream process development, cell/virus banking, GMP biologics manufacturing, GMP aseptic filling, QC release and stability testing, etc., to biopharmaceutical clients is required.
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Maravai companies are global leaders in providing products and services into 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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Knowledge and experience with HCP Elisa, Residual DNA testing, Protein A testing, method development for biologics, and method validation and transfer. A solid foundation in biologics manufacturing process development and exposure to biologic impurities within commercial manufacturing is preferred, but not required.
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BCBBS:Board Cert Biologics and Biosimilars Spec. Serves in specialized leadership function such as but not limited to Residency Program Coordinator, Pharmacist in Charge, entity stewardship or operational function or Investigational Drug Services at least 50% of the time.
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A deep knowledge of cancer biology and immune-oncology and drug development across different modalities - small molecules, biologics, gene, and cell therapy. We are supported in this mission by top Silicon Valley and New York venture firms that are leaders in the healthcare space with extensive experience in supporting precision medicine companies such as Foundation Medicine and Guardant Health.
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Familiar with current regulatory guidance and industry best practices for development and validation of bioanalytical methods for large molecule biologics. A minimum of 5 years of hands-on experience in the development and validation of quantitative immunoassays and immunogenicity assays for biologics (e.g. antibodies, proteins or peptides.
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Provide strong expertise in biophysical characterization techniques & instrumentations, such as SEC-MALS, CD, DSC/DSF, FT-IR, AUC, DLS, Raman, in-silico modeling for biologics characterizations.
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We are seeking a dynamic and results-driven Business Development Director to lead our efforts in selling Cell and Gene Therapy (CGT) and Biologics services. Business Development Director - CGT & Biologics Services.
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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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LOTTE BIOLOGICS entered the biologics CDMO business after acquiring Bristol Myers Squibb’s Syracuse biologics drug substance manufacturing site, as of January 1, 2023! We are LOTTE Biologics.
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AbbVie Director, Early Phase Analytical Development in North Chicago , Illinois The Biologics Analytical R&D (ARD) group develops antibody drug conjugates (ADC) and other therapeutic biologic medicines by developing analytical methods and providing analytical results to support drug substance and drug product process and formulation development.
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Just - Evotec Biologics' Bioreactor Process Development group is seeking an enthusiastic and hardworking team member who is passionate about expanding worldwide access to biotherapeutics through the advancement of continuous bioprocessing technology and mammalian cell culture processes.
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The Senior Associate Scientist position is part of the Global MSAT Pilot Lab Cell Culture team in the drug substance function within global Manufacturing Science, Analytics and Technology (MSAT) and is based at the biologics hub in Framingham, MA. MSAT's mission is to enable the reliable supply of Specialty Care (SC) medicines by providing expert technical and scientific support to their licensure, ongoing commercial manufacturing, and life-cycle management activities.
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This will include formulation and commercial process development for biologics (monoclonal antibodies, antibody drug conjugates, bispecifics and fusion proteins). The Biologics Drug Product Development group develops monoclonal antibodies, antibody drug conjugates (ADC), and other biologics using state of the art formulation and process technologies.
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The individual will play a hand-on execution role in the routine operation of the Biological pilot plant whose purpose is to produce material for preclinical, clinical, and commercial biologics drug substance to support Clients pipelines.
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