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The Associate Scientist s expected to design, develop, and execute purification processes to meet early-stage process development objectives and timelines. Summary of the group: The Biopharmaceutical Development group is a multi-disciplinary scientific function providing expertise in Process/Analytical/Formulation/Devices Development and Characterization with integrated Bioprocess Engineering, Clinical Manufacturing, and Supply Chain and Logistics operations.
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Research in Upstream Process Development centers on the identification and optimization of process parameters to support and control the growth of a mammalian or microbial cell line in a production bioreactor.
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Research Associate, Downstream Process Development - Contract - Gaithersburg MDProclinical is seeking a Research Associate to support a temporary surge in Downstream Process Development.
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We are seeking a talented and experienced Scientist III/Principal Scientist to join our Upstream Cell Culture Process Development Team. The ideal candidate will lead technical aspects of cell line development and upstream cell culture activities for antibody-based pipeline programs with a specific focus on antibody drug conjugates (ADCs), bispecifics, and fusion proteins.
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EchoStar has an exciting opportunity for a Process Engineer - Surface Mount Technology (SMT) with our Hughes Network Services Manufacturing division. Work with managers and supervisor to improve process for Surface Mount Technology and Box Build Departments.
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Assure product and process quality by designing test methods, testing finished product and process capabilities, establishing standards, confirming manufacturing processes. Our complete array of food packaging serves a variety of markets, including fruit, vegetables, dairy, fish, meat, ready meals, pet food, infant milk powder and other dry food products.
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Qualified individuals will be responsible for hands-on execution of downstream chromatography and filtration processes in support of process development, scale-up, process characterization activities, and technical support of cGMP manufacturing for proteins, nanoparticles, and virus-like particle (VLP) based vaccines.
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10+ years of experience in process engineering preferred, with at least 10 years in a leadership role within the biotechnology or pharmaceutical industry with a focus on cell therapy or biologics.
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Act as subject matter expert in Upstream Process Development of biologics including, but not limited to vaccines, viral vectors and recombinant proteins. + Teaching others in their area of expertise, and assists with work being performed by other members of the Upstream Process Development group.
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The Manager is responsible to follow and direct the requirements of TMC Quality System related to engineering and process control systems; including but not limited to: process controls, calibration and maintenance practices, document/data control, change control practices.
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Experience in leading large-scale process development, hindsight and training workshops. Partner w/GTM and Marketing Leadership to create process development roadmaps which prioritizes new projects in context of pre-existing workload, available resources and timing requirements.
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Working knowledge of the broad range of biologic CMC disciplines (upstream & downstream process development, purification, formulation & delivery technologies). Applies a fundamental understanding of mammalian cell culture operations to support upstream bioprocess development activities including technology development, yield and process optimization, and process characterization studies.
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The Process Development Scientist I – Upstream is responsible for studying properties of mammalian cell culture, developing new assays, and exploring new methods for viral vector production within the department of Process Development.
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2+ years of experience improving process for Surface Mount Technology and Box Build Departments. Conduct system tests to verify efficiency, accuracy and production process is successful.
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Support improvements using lean/six sigma principles to enhance quality, additive, and assembly process. Ability to relentlessly triage multiple process root causes simultaneously. Knowledge of Process Certification/Process Robustness.
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Title: robotic process in Germantown, MD
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