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They will drive scientific, technical, and executional excellence in the development and technology transfer of assays (immuno-, molecular, cytometry, and cell-based assays) used in the characterization and quality control of our TCR T cell therapy products and intermediates.
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To support product/process development and submission, site transfer, validation, equipment qualification and packaging studies. 4-7 years of Pharmaceutical Manufacturing or Technical Services/Validation/Process Development related experience.
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Just - Evotec Biologics' Bioreactor Process Development group is seeking an enthusiastic and hardworking team member who is passionate about expanding worldwide access to biotherapeutics through the advancement of continuous bioprocessing technology and mammalian cell culture processes.
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Advance enabling technologies to accelerate pharmaceutical development and to improve sustainability and process efficiency, including advances in biocatalysis, high-throughput technology, flow chemistry, and AI/machine learning.
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Engineering Facilities operations, technology development, or process technology transfer. As the Electrical, Instrumentation and Controls Area Manager , you will be responsible for the safe, reliable, and cost-effective operations of the Oregon development factories, the development of new enabling, hardening, or energy conservation projects related to the electrical disciplines, the successful transfer of technologies to HVM sites within the network, and the support of construction ramps in Oregon and receiving factories.
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Strong understanding of QMS business processes, Manufacturing, Development Technology Transfer process, Computer System Validation. Additional Experience in the following would be preferred but not required: o Veeva Vault Quality, Trackwise, Veeva Quality Docs, Kneat Validation Execution, Metric Stream, Process PLM in Manufacturing and Qualityo Manufacturing Execution System (MES) or manufacturing systems integrations i.
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Transfers and Introduces technology of cell therapy-based and therapeutic protein processes into manufacturing collaborating extensively with Scorpion’s Process Development group to develop cGMP-compliant, clinical-scale production processes.
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Incorporates product and process changes in Tech Transfer documentation. You'll be able to make a big contribution to our work at the nexus of technology, farming, and the global food industry - and we're only getting started.
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Strong business acumen with an understanding of financial implications of new process technology development, scale up, process improvement, and risk. Lead monthly reviews of operations (Incinerators, Refineries, Transfer Storage/Disposal facilities, Wastewater Treatment, and Landfills) key programs/initiatives to drive timely development and execution.
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Providing routine troubleshooting and maintenance of process development instruments including reactors, HPLCs, purification skids and UF/DF manifolds. Successful candidates will be a part of a dynamic and enthusiastic team responsible for development, scale up and tech transfer of the ECO Synthesis™ platform.
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Sound knowledge of cGMP practices as applicable to process development, scale up, technology transfer, formulation development, and Manufacturing. This role will support the tech transfer and process development through the application of processes, procedures and technologies in the development of best-in-class vaccine scale up and manufacturing.
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Knowledge of biologics regulatory guidelines including FDA/ICH on risk management, technology transfer and process validation. This position will report to the Head of Purification Process Development and Manufacturing.
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Responsible for management of complex Process Development and Good Manufacturing Practices (GMP) Manufacturing projects spanning from initiation of technology transfer through commercial operations, enabling successful project execution throughout the project life cycle, and accountable for providing mentorship to junior project management professionals who maintain a portfolio of Process Development and GMP Manufacturing projects.
$115,000 - $125,000 a yearExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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As a Thin Film Process Development Engineer in our Technology Development Group, you will join an existing team of engineers responsible for developing, characterizing, and transferring process solutions for advance DRAM applications.
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Provide front line and independent process development expertise for clinical and commercial drug product manufacturing operations during sterile processing, process characterization, tech transfer, process validation, and on-going commercial manufacturing.
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