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Drive technology transfer activities, ensuring phase-appropriate process development and scale-up for seamless transition to manufacturing. As a key member of the team, you'll collaborate cross-functionally to ensure the seamless transition of processes from R&D formulation development phase to commercialization, while adhering to strict regulatory guidelines.
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Work with new equipment/develop studies with equipment that could improve soft chew manufacturing process and/or formulation. Cooperate with PD staff in preparation/execution of pilot batches and product scale up batches and gather data to support in-process parameters and finished product specifications.
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Biotech manufacturing, Cell Culture, depth and tangential flow filtration, column chromatography, protein purification and formulation, buffer and media operations, SOP. Knowledge of biotech manufacturing processes and equipment, including cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation, and buffer and media operations.
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Incumbent will partake in clinical scale cell processing including isolation, culture, and formulation, tissue culture using sterile technique and universal precautions and assays with primary human cells from study subject in support of cell and gene therapy clinical trials at the University of Pennsylvania as well as basic immune biology studies.
$37,220 - $57,335.4 a yearFull-timeExpandUpdated Today - UpvoteDownvoteShare Job
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Knowledge of biotech manufacturing process and equipment including cell culture, depth and tangential flow filtration, column chromatography, protein purification and formulation and/or buffer and media operations.
$28 - $32.2 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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From IND applications through commercial scale production, we provide formulation and compounding, fill-finish, and optional lyophilization services for a wide variety of liquid injectables.
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Demonstrated expert knowledge in DS and/or DP manufacturing and scale-up of small molecule compounds (organic chemical synthesis, crystallization, chromatography, filtration, precipitation, drying, API formulation, spray drying, milling & micronization, API physical characterization, blending, compaction, film-coating, encapsulation, tableting and typical analytical tests for OSD products.
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Ensure that CRO/CMO activities and other process development activities address drug substance needs for pharmaceutical formulation development, toxicology testing, clinical trials, and commercial launch.
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Working knowledge of CMC upstream process development, analytical development, formulation development, bioconjugation process development, technology transfer, and GMP quality requirements. Apply technical knowledge and expertise in downstream process development (chromatography purification, viral filtration, TFF, etc), unit operation scale up, and technology transfer to advance biological drug candidates across the product life cycle.
$131,500 - $195,500 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Hands on work will be required in small and large scale including, but not limited to, upstream, downstream, conjugation, formulation and lyophilization processes as needed. Assist technology receipt of Production, purification of Polysaccharides, proteins, bulk conjugates and vaccine formulation technology from R&D and their transfer to large scale manufacturing using different state of the art techniques.
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Coordinates strategic planning, new concept exploration as it relates to the NAS and NextGen, development, prototyping, demonstration, and initial requirement definition to support investment decisions, policy formulation, and full-scale development on future NAS systems with special emphasis on development of NextGen. Requirements Conditions of EmploymentUS Citizenship is required.
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The vice president of product development will be responsible for leading flavoring and formulation, as well as the program management to bring all products (line extensions, existing products, innovation) through commercialization (including scale up so that it is ready for manufacturing.
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Lead and oversee scientific, strategic, planning and execution of biologics formulation development, drug product development and validation including process selection and scale-up, packaging and labeling development, technology transfer, and drug product characterization.
$128,000 - $165,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Will play a key role in leading the design, optimization, and scale-up of manufacturing processes for cutting-edge drug products. Apply now to join our client's dynamic team as a Principal Process Development Engineer and embark on a rewarding career journey.
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Apply cross-functional problem-solving skills in regards to food formulation, new technology application (i.e. 3D printing), bench-to-pilot scale-up, and other types of food manufacturing machinery.
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