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Knowledge of cGMP for pharmaceutical and/or vaccine manufacturing, Lean Six Sigma Methodology, Root Cause Analysis, Failure Mode Effects Analysis, knowledge in reliability engineering (including asset life cycle management.
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6+ years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, and bulk formulation. As Gene Therapy Manufacturing Supervisor, you will play a critical role in helping to establish REGENXBIO's first internal GMP BDS and FDP clinical and commercial AAV gene therapy manufacturing capability.
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The Vaccine Manufacturing Facility Production Associate is an excellent opportunity for experienced individuals that are interested in working in vaccine production and manufacturing operations.
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You will provide day-to-day engineering support for assigned area which may include vaccine bulk manufacturing, filling, lyophilization, packaging, and/or mechanical support utilities including power, HVAC, steam, WFI and controlled temperature units.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Join FDB and help create the next vaccine, cure, or gene therapy in partnership with some of the most innovative biopharma companies across the globe. The Manufacturing Supervisor may be assigned to work directly with Upstream, Downstream or Buffer Preparation Unit Operations.
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Responsible for supervising daily manufacturing activities and staff, including hiring, performance, evaluations, coaching, mentoring, disciplinary actions, termination recommendations, training, development, etc.
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Seqirus has an exciting opportunity to join our expanding team in Holly Springs, NC. With an advanced manufacturing facility and expertise in influenza science we are one of the world leaders in the production of the influenza vaccine.
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Bachelor of Science in Chemical Engineering, Biotechnology, Mechanical Engineering, Biochemistry, Protein Chemistry, or related field with at least 5 years of experience in vaccine and/or biopharmaceutical Development, Process/Product Development, and/or Biological manufacturing or closely related field.
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This position will support Quality Control clinical testing activities for cell and gene therapy clinical trials to treat patients with cancer and HIV supported by the Clinical Cell and Vaccine Production Facility (CVPF) at the University of Pennsylvania.
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Under limited supervision, the Technician II/III, Process Maintenance executes advanced maintenance activities for assigned vaccine manufacturing equipment such as: cell culture and fermentation tanks, pumps, chromatography skids, ultra-filtration skids, centrifuges, CIP / COP units, glass washers, autoclaves, freeze dryers, depyrogenation ovens/tunnels, vial fillers, high-speed labeling and packaging systems, and other equipment.
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Experience with vaccine upstream process development. Characterization studies for tech transfer to manufacturing partners. Meet’s partnered with an East Coast-based vaccine pharmaceutical company on an exciting new search for a.
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These instruments are essential tools in the research, development, and manufacturing for several key areas including Cell and Gene Therapy, Infectious Disease, Virology and Vaccine Research, Immunology, Immuno-oncology, and Immunotherapy, as well as Next Generation Sequencing, and Pre-Natal Disease Detection.
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Possesses working knowledge in downstream processing for vaccine production, e.g. Lyophilization, Tangential Flow Filtration, Centrifugation, Emulsification, Filling, etc. Possesses working knowledge in vaccine antigen production processes, e.g. Tissue Culture, Fermentation, Chicken Embryo Origin Processes, etc.
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Working knowledge of statistical methods for DOE design and data analysis, statistical process control (SPC), multivariate analysis (MVA), and/or process analytical technologies (PAT) techniques for manufacturing processes.
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Experience in media development in biopharma, cell & gene therapy and vaccine manufacturing. Knowledge of cGMP & regulatory standards for biopharma manufacturing. Experience in media development in biopharma, cell & gene therapy and vaccine manufacturing.
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