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3+ years of experience in the pharmaceutical industry within a GMP Quality Control role; experience with cell therapy products is a plus. Minimum of 2 years experience in the pharmaceutical industry working in a GMP quality control laboratory.
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Excellent knowledge of the Keystone STARS program and the performance standards including all relevant databases and supportive services available in the system such as the ECE PDO, EITA, IECMH, and local quality improvement programs.
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Morgan, Lewis & Bockius LLP, one of the world's leading global law firms, with offices in strategic hubs of commerce, law, and government across North America, Asia, Europe, and the Middle East, is seeking a Quality Assurance Test Manager to lead the execution of Morgan Lewis Information Technology Department's software test strategy to ensure that our Technology solutions, whether COTS or custom in-house applications, exceed our end users' expectations of quality and reliability.
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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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The Project Manager/Senior Project Manager is responsible for overall management of clients and projects including design, communications, personnel management, budgets, schedules, quality control, business development, and client communication & relationships.
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Oversee all phases of project management including mass excavation, site development, demolition, fine grading, pipe and drainage installation, traffic control, structure demolition and removal, underground utilities, erosion control, concrete work, steel work, and paving and milling.
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Quality control and operation of the Angiography System in a safe and competent manner supporting the ALARA principles and alerting the physician of intra-procedural dose thresholds and equipment trouble shooting.
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Support technical problem solving for issues pertaining to GMP Quality Control. Perform daily GMP Quality Control laboratory testing activities at the iCTC facility with minimal to no errors while ensuring testing is completed in compliance with all applicable procedures, standards, and GMP regulations.
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The CRU Regulatory Affairs Office seeks a full-time Regulatory Affairs Veeva Quality Assurance Specialist to participate in the review and migration of Phase I-V clinical trial investigator site files to the Veeva SiteVault platform.
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Tasks include performing systems engineering analysis to interface control systems with other new or modified shipboard systems, troubleshooting control system hardware issues at the Land Based Engineering Site/Test Facilities (Philadelphia, PA), and upgrading the cyber security features of the existing and future Control System (CS/IS) variants.
$74,500 - $130,400 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Perform Quality Control and Quality assurance activities to verify and maintain accurate and complete protocol metadata in Clinical Research Systems. Temple Health consists of Temple University Hospital (TUH), Fox Chase Cancer Center, TUH-Jeanes Campus, TUH-Episcopal Campus, TUH-Northeastern Campus, Temple Physicians, Inc., and Temple Transport Team. Temple Health is proudly affiliated with the Lewis Katz School of Medicine at Temple University.
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The Supplier Quality Specialist executes qualification, maintenance, and monitoring for WuXi suppliers with an emphasis on continuous improvement, global alignment, risk management, and supply chain reliability.
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Minimum three (3) years of experience in the pharmaceutical industry within a Quality Control roleExperience with two or more of the following: Flow Cytometry, Cell based ELISA, NC200. The Quality Control testing programs include, but are not limited to, in-process, final drug product, and stability testing with a focus on cell therapy products.
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Notify Infection Control Coordinator immediately of suspected or confirmed cases of communicable disease. Observe ambulatory care guidelines for infection control (hand washing, care of environment, use of safety syringes and sharps containers, use of personal protective equipment.
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The scope of work will encompass high level engineering designs ranging from 4kV - 500kV. Position will be responsible for development of physical layout of equipment, protection and control logic, elementary and wiring diagrams supervision of subordinate engineers and designers to assure the quality of design deliverables.
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quality control jobs Company: Cepheid in Philadelphia, PA
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