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Represent Drug Product team in CM&C teams and support the formulation and process development of protein, peptide, oligonucleotides and other novel modalities in clinical development.
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Great working knowledge of formulation development, drug development and clinical development. Work with formulation development groups and provide support for activities related to formulation development, dissolution testing, in vivo-in vitro correlations and biowaivers for pre- and post-approval formulations.
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Ph. D. in pharmaceutical sciences, chemical engineering, physical-organic chemistry, or related field, and three years of experience in pharmaceutics, solid dosage formulation development, drug delivery technology, and processing technologies.
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Pharmaron is a premier contract research organization that offers a broad spectrum of R&D and manufacturing service capabilities throughout the entire drug discovery, preclinical, clinical development and commercialization process.
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AnTolRx, Inc. is seeking a highly motivated Scientist/Senior Scientist to join its research team in Cambridge, MA. The ideal candidate has a strong background in lipid nanoparticle formulation and drug delivery, is a self-starter, and is looking to make a significant impact on our cross-disciplinary team.
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The successful candidate will be a member of the Genomic Medicine Drug Product Development group within Injectable DPD. This individual will have a direct impact on a dynamic and growing group of scientists and engineers developing adeno-associated virus (AAV) based gene therapy products within the larger Alexion Rare Disease Business Unit organization.
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Establishing cross-functional relationships with Sarepta Analytical Development, Formulation Development, and Process Development groups. Designing, performing, and/or overseeing the execution of stability studies of critical materials, intermediates, drug substance and drug product related to the company's AAV gene therapy and RNA PMO product pipelines.
$180,000 - $225,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Experience in formulation development of lipid nanoparticles and other Client drug delivery systems is preferred." We seek an outstanding candidate to join the formulation screening efforts in the Synthetic Molecule Analytical Chemistry Development.
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Experience working with mRNA technologies, HPLC analysis, and pre-clinical to clinical drug development is a plus. D. in Drug Delivery, Nanoparticle formulation or related discipline with 0-2 years research experience in an industry environment.
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As an expert in the areas of preformulation and formulation development studies, drug delivery technologies, and product development, this position will be responsible for providing guidance, oversight, and mentoring to a team of scientists.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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An individual at the level of Principal Scientist, Oral Formulation Development will lead projects as an individual or build a team focused on oral formulation development for small molecule or peptide drug products and amorphous intermediates.
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Lead formulation development of mRNA drug targets entailing: LNP formulations for in vitro/in vivo studies. Work closely and build relationships with select CROs with focus on in vivo studies, drug carrier design/development, assay development.
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Calibr-Skaggs supplements the discovery process with the required disciplines for drug development which include chemical library screening, medicinal chemistry, in-vivo model optimization, formulation development, pharmacokinetic and toxicologic expertise, and early clinical development.
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We focus on bringing client drug compounds from discovery to the clinic with services that include analytical development, pre-formulation testing, formulation development, GMP manufacturing and stability storage and testing as well as Clinical Supply Services.
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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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