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Direct and oversee the downstream request for proposal (RFP) and bid process and prepare detailed scope of work documents for subcontractor and client contractor contracts, including bidder development, prequalification, evaluation, award recommendation, and selection.
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We’re driving the company’s digital transformation and expanding business capabilities using industry best practices and advanced technologies such as cloud, artificial intelligence and robotics process automation.
$100,000 - $160,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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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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Since its founding in 2016, Galehead has deployed its proprietary LandCommand® technology and specialized upstream platform to develop more than 15 GW of solar, storage, and wind projects under active development by Galehead and its Downstream Partners including Tyr Energy Development, EDF, Clearway, Rev Renewables, Steelhead, Engie, and Longroad.
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Experience with some or all of the following: cGMP manufacture and/or process development for CAR T, TCR, NK, cellular therapies, AAV, LV, RV.Advanced understanding of primary cell culture and experience with equipment such as CliniMACS Plus, CliniMACS Prodigy, LOVO, bioreactors (single-use and fixed-bed), chromatography skids, TFF (hollow-fiber and flat-sheet) and WAVE bioreactors such as Xuri, G-Rex system.
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Associate Director, Downstream Process Development. Associate Director, Downstream Process Development. Principal Scientist, Platform Technology. Associate Scientist II, Translational Biology.
ExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Prepare Request for Proposal (RFP), support detailed scope of work development, bid and selection process, and creation of contract documents for the purpose of subcontractor and client contractor selection and award.
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10+ years of experience in biologics process development with a strong understanding of antibody processing, including upstream and downstream processes. Job Overview: Looking for a driven and skilled manager to lead our client’s drug process development and manufacturing team, overseeing internal and external processes to support their clinical development portfolio and contribute to bringing new therapies to patients.
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Promote and develop process improvements for clinical sample lifecycle management including specimen collection, tracking and downstream storage and/or destruction. Prepare and review key study start up documents such as clinical study protocols, clinical kit development, lab manuals and consent forms, and to verify that biological samples are collected as specified in the protocol and related plans.
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Scientist - Downstream Process Development. We are seeking a highly skilled and motivated Scientist to come join our CMC, Process Development team and help drive our clinical trials to market.
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The ElevateBio ecosystem combines multiple R&D technology platforms including Life Edit, a next-generation, full-spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non-viral therapeutic delivery platform with BaseCamp, its end-to-end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics.
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The Director will be primarily responsible for scientific leadership and technical oversight of upstream and downstream process design, development, and scalability of unit operations necessary for supporting the Target product profile of the vaccine candidates in development.
$200,000 - $240,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Your primary role involves management and hands-on research including purification process development and analytical development / characterization of mRNA and circRNA, with the ultimate aim of producing therapeutic-grade material for in-vitro downstream assays and deliver scalable purification strategies to reduce immunogenicity and maximize in-vivo expression.
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Prepare Request for Proposal (RFP), support detailed scope of work development, bid and selection process, creation of contract documents for the purpose of subcontractor and client contractor selection and award.
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downstream process development jobs in Boston, MA
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