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Ideally experienced in 1 or more of the following: facilities and equipment startup, walk downs & troubleshooting, utilities (WFI, RO, HVAC) upstream, downstream, purification, recovery, building automation or other pharmaceutical manufacturing processes.
$87,100 - $94,600 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The Research Production team is responsible for the upstream enzymatic synthesis and downstream manufacturing of drug substance to support pre-clinical trials. Downstream experience with standard chromatography and/or DNA purification kits is a plus.
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A successful candidate will help with in-house manufacturing of key materials and optimize our production process to support manufacturing DNA gene therapy molecules. Directly assist in the planning and execution of laboratory experiments to develop manufacturing and purification of closed ended DNAs using the RES process.
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This position is part of the Downstream Hardware Modality located in Bioprocess and will be fully remote. The Downstream Hardware Field Application Specialist for Cytiva is responsible for providing technical expertise during pre-sales discussions, instrument demonstrations, customer training, post-sales support, seminars, and promotional events.
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The individual will execute relevant protocols to purify therapeutic oligonucleotides suitable for downstream in vivo studies. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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High level of downstream experience formulating a wide range of products such as creams, lotions, solutions, serums, mousses, surfactant systems, and aerosols. Support tech transfer to third party manufacturing facilities for scale-up and production, including identifying and generating appropriate product specifications.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Lead new sourcing and new manufacturing capabilities initiatives based on hardware product roadmap. Leverage DFM/DFA skills to influence product decisions and communicate the downstream operational impacts of design.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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We love experienced generalists, but if you’re a CQV SME in facilities, clean utilities, upstream and downstream biotech equipment, single use disposable, or aseptic fill finish manufacturing, we’d like to talk to you.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Demonstrated knowledge of cGMP manufacturing with knowledge in manufacturing operations in downstream processing utilizing single use technology (SUT). Review production documentation and perform quality walk-throughs during manufacturing events.
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Responsibilities: Lead event investigations to adequately identify root cause and implement appropriate corrective and preventative actions to prevent reoccurrence, Lead CAPA investigations and at times manage the implementation of CAPA. Own manufacturing related change controls.
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Renewable Energy Semiconductor Manufacturing. 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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The Associate Director/Director Upstream Process Development and Technical Operations will be directly responsible for the process development and technical manufacturing elements of AVEO’s biologics drug substance programs.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Perform routine right-first-time cGMP manufacturing of cell and gene therapy products including but not limited to aseptic processing, cell isolation, selection, culturing, cryopreservation, upstream processing, downstream processing, aseptic fill finish and final product visual inspection.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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You'll collaborate closely with our Process Liquids Solutions Technical Sales Executives (TSEs) to identify and cultivate opportunities for custom cGMP process liquids manufacturing services, aimed at simplifying bioprocess workflows both upstream and downstream.
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Perform small-scale purification process including ultracentrifugation, column chromatography, cell lysis, clarification, AKTA and TFF unit operations, and depth filtration for manufacturing of LVV gene therapy vectors across multiple preclinical programs and disease areas to ensure on time delivery.
ExpandApply NowActive JobUpdated 8 days ago
downstream manufacturing jobs in Boston, MA
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