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We are seeking a Principal Research Scientist II to conduct process research and development of antibody-drug conjugates from pre-clinical through clinical development. The successful candidate will have a strong understanding of process development, control strategy development, regulatory starting material strategies, specification setting, QbD principles, tech transfer and process validation requirements.
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The Scientist IV, Bioconjugation (ADC) Process Development, will have an opportunity to contribute to Exelixis' Antibody Drug Conjugates (ADCs) technology platforms. Develop Subject Matter Expertise in bioconjugation (ADC) process development and manufacturing in support of CMC activities.
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Must possess broad analytical chemistry knowledge in HPLC, GC, UV, FTIR and other related analytical technologies and/or broad knowledge of development and manufacturing of MDI/DPI/Nasal products.
$43.27 - $48.08 an hourExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Working with the Safety Support Personnel in the development of the NEPA, ISO and Pollution Prevention and Waste Minimization forms and any other environmental components of the SARS package. Support document drafting, sharing, organizing, and archiving to support RIC SME engagement on the IPT. Documents will include:Technical specifications and requirementsSafety program documents (plot plans, process flow diagrams, hazard charts, process and instrumentation diagrams, and others)Acquisition related items including vendor quotes, sole source justifications, acquisition requirements, and othersOther documentation required by the IPT to fully execute its functions.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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VCGT is seeking a Cell Therapy Process Development Scientist for the T1D drug substance group. Scientist, Process Development Engineering. The focus of this position is to drive embryonic stem cell process development, process characterization, and verification.
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CBP OPR seeks a team in support of the Reporting and Development Program (RDP) which will review OPR’s current business and workflow processes and collaborate with CBP JICMS developers, OPR leadership and end users to identify and implement modernization enhancements which close process and data gaps while ensuring quality assurance of reported data.
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The Scientist-In Vitro ADME is responsible for performing a variety of technical procedures and experimental execution in support of sample analysis, method development, and validation. ;General awareness of the drug development process and the interaction of method development in that process.
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Experience with: HPC and distributed large model training; GPU performance optimization; or end-to-end model development, particularly in LLMs. Projects may include any area of the quant research process with the potential from business-wide application.
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Responsible for route scouting, process development and manufacture of intermediates and target compounds up to 100 L reactor scale. 0-3 years of industry experience in chemical process development and manufacturing.
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Process Development Scientist (Formulation & Drug Product Development) In this vital role you will support Formulation & Drug Product Development at Amgen's site in Rockville, MD. This group is responsible for drug product formulation and process development for biologics in Amgen’s Rare Disease Business Unit. Working closely with a team of scientists and engineers, the successful candidate will apply scientific and engineering principles to advance the technical aspects of Amgen’s drug product and process development.
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As a Food Scientist , reporting to the R&D Manager on our Food Service Frozen Meals team, you will work on innovation and product development for our frozen multi-serve meals for our internal brands as well as key national accounts.
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This position requires an individual with scientific knowledge of HEOR and its application throughout development process, business insight, and interpersonal skills. The Senior Scientist reports to the Asset Lead, Oncology Outcomes Research, and will be responsible for leading the execution of health outcomes and real-world strategies and studies on a global and US market level.
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We are seeking an Applied Scientist / Data Scientist with deep expertise in machine learning, artificial intelligence, including the development and deployment of large language models.
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Provide directions and energy, carbon footprint assessment leading to optimum technology selection for low carbon Ammonia, urea development, and technology configuration of the process. Lead/Staff Scientist Life Cycle Assessment is expected to have demonstrated expertise in estimating the LCA of various products including Ammonia, Urea and Enhanced Urea from Cradle to Grave.
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If applicable, supports the clinical drug development process as a BDS Product Owner up to the level of substance/assets. Supports the clinical drug research and development process by providing strategic planning and execution, including data transformation and all aspects of descriptive, diagnostic, predictive and prescriptive analytics of data related to clinical projects like actual trial data, registries and real-world data bases.
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