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The QA Specialist is responsible for all aspects of Quality Assurance related to internal processes and manufacturing activities that will take place within the DFI cGMP Facility. The Duchossois Family Institute (DFI) at the University of Chicago seeks a Quality Assurance Specialist for our current Good Manufacturing Practices (cGMP) facility.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Responsible for development, execution & analysis of validation projects to demonstrate equipment, utility, and facility cGMP/QSR compliance. This position is responsible for development, execution, & analysis of validation projects to demonstrate facility, utility, equipment, and process consistency and cGMP/QSR compliance.
ExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Selection of suitable plasmapheresis donors by performing physical examinations and taking medical histories on all donors through the use of FDA approved Standard Operating Procedure (SOP) Manual, current State and Federal guidelines, OSHA, CLIA, CGMP, all internal company procedures and personal education and experience.
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Assists in the transfer of technology from Process Development to cGMP Manufacturing. Completes Batch Records and other cGMP documentation accurately and in a timely manner. Must comply with Kashiv BioSciences policies, procedures (SOP), FDA current Good Manufacturing Practices (cGMP), and any other government requirement.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Maintain compliance with SOP, current Good Manufacturing Procedures (cGMP) and regulatory guidelines. Maintain compliance with SOP, current Good Manufacturing Procedures (cGMP) and regulatory guidelines.
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Manage incoming inspection of raw material for cGMP use. Prior experience with CMC regulatory activities and/or agency (FDA) interactions in the development of advanced biologics. This facility will be a first of its kind, state-of-the art, adaptable microbiome manufacturing center embedded at the interface of a world-class microbiome sciences research team and patient-centric medical center aimed at translating innovation at the bench to investigations in the clinic.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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The Bio-Processing Engineer is responsible for all aspects of microbiome drug substance process development that will take place within the DFI cGMP Facility. The Duchossois Family Institute (DFI) at the University of Chicago seeks a Bio-Processing Engineer for our current Good Manufacturing Practices (cGMP) facility.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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The company focuses on producing cell culture products, instruments, and solutions that help customers streamline their discovery, development, and production processes, and by making custom cGMP bioprocess liquids that radically simplify customers' manufacturing workflows - regardless of batch size.
RemoteExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Learn and maintain thorough familiarity and compliance with all state and federal regulations, U.S. Food and Drug Administration (FDA)-approved Standard Operating Procedure Manual, Occupational Safety and Health Administration (OSHA), Clinical Laboratory Improvement Amendments (CLIA), Current Good Manufacturing Practice (cGMP) and internal company procedures.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Sr. Supervisor, Manufacturing Operations (Chicago, IL): Be responsible for oversight of pharmaceutical manufacturing processes; producing high quality pharmaceutical products in accordance with regulatory requirements to achieve the operations production plan; as well as oversee daily supervision of personnel on the efficient use of equipment and materials to produce quality products under cGMP in accordance with the production plan, including scheduling and resource coordination.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Degree) in Pharmacy, Pharmaceutics, Pharmaceutical Science or related with knowledge of IQ, OQ, PQ, preparing standard protocols & reports for testing & analyzing Injectable products; as well as overseeing & managing regulatory compliance.
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Ensures documentation meets facility audit as well as cGMP or GLP requirements. Background in HPLC and other analytical techniques (GC, AA, UV, TLC, and wet chemistry) desirable. Job Summary The Associate Scientist is responsible for performing entry level chemical testing to support raw material, in-process, stability, and finished products as required for Quality Control.
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Ensure all calibration and thermal mapping activities comply with relevant industry regulations (e.g., FDA, cGMP). Strong understanding of regulatory requirements (FDA, cGMP, CFR part 210/211, CFR part 820, etc.
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Complies with cGMP, EHS guidelines and all working procedures assigned to the position. Sets up and operates lathe, drill press, grinder, and other metalworking tools to make and repair parts.
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With donation centers and team members throughout the U.S., Octapharma Plasma, Inc. collects plasma to create life-saving medicines for patients worldwide. There are so many ways Octapharma Plasma can enhance your life and your career.
ExpandApply NowActive JobUpdated 6 days ago
cgmp job in Chicago, IL
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