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As part of Our Company's Manufacturing Division, within the Manufacturing System Design & Commercialization, the Biologics Process Development & Commercialization department provides the technical process leadership and laboratory capabilities in support of late stage pipeline and commercial manufacturing processes for biologics (therapeutic proteins.
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Cross-train on and provide support for upstream and downstream process development operations. Support viral vector process development and production by designing and performing fast and robust assays for the characterization of AAV.
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The Senior Scientist I will play a key role in the developing downstream purification process development for various modalities such as mAbs, ADCs, bio-specifics, gene therapy, etc.
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Lead an integrated process development, analytical development, and manufacturing team across upstream and downstream functions for mRNA production. This position will play a critical role in ensuring the supply of mRNA that meets quality requirements for use in manufacturing Cartesian's mRNA cell therapy programs at multiple stages of clinical development.
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10+ years Downstream Process Development experience related to biochemical engineering and/or protein biochemistry, scale-up principles, and manufacturing of Biopharmaceuticals (cGMP.
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As a Process Development Scientist II, you will help our clients to deliver lifesaving and life changing therapies to patients in need. Knowledge of gene therapy product and/or process development preferred.
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Support tech transfer of new products and processes to ensure smooth transition from process development/clients into GMP manufacturing. Partnering with Process Development and Operations to meet the production schedule, ensure product supply and uphold quality standards.
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Hands-on protein purification and downstream process development at scales from 0.1-50 L. The Research Associate III is a part of the Downstream Bioprocess Development department and responsible for designing, performing, and analyzing experiments to establish, understand, and optimize enzyme purification processes.
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Prior experience with mRNA upstream and downstream process development. The incumbent will be responsible for the mRNA synthesis, purification, formulation, and analysis to support the process development of mRNA production in various scales.
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And with proteins expressed in mammalian cells with oversight of both upstream and downstream process development. Principal Scientist, Protein Production and Process Development.
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BPR&D includes three lab-facing technical functional areas: Process Cell Sciences (PCS), Upstream and Downstream Process Development & Engineering. Beyond process development for pipeline biologics, we innovate and build next generation biomanufacturing technologies.
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Executes experimental studies to develop, optimize, or characterize cell line development, upstream or downstream processes for therapeutic protein candidates under supervision (60-70%) The development intern is responsible for performing assigned experimental tasks to support the development or optimization of upstream or downstream processes for Alexion’s therapeutic protein candidates.
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The latter two together form our Biologics’ Process Development (BPD) group. Biologics Process Research & Development (BPR&D) within our Research Laboratories is on a mission to rapidly deliver diverse biotherapeutics to patients by efficiently developing innovative, robust manufacturing processes and technologies.
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Novavax is seeking a Senior Scientist to join our Downstream Process Development group in Gaithersburg, MD. Qualified individuals will play a leading role in downstream process development and process characterization activities, new technology evaluation, and technical support of cGMP manufacturing for proteins, nanoparticles, and virus-like particle (VLP) based vaccines.
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The Engineer/Scientist, Protein Development is responsible for research and process development in our enzyme program using conventional fermentation and purification methods. Development of new and optimization of existing industrial enzyme fermentation, downstream processing (DSP), and formulation processes based upon quality by design (QbD.
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