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As the chief clinical training site for the Lewis Katz School of Medicine at Temple University, the hospital provides a dynamic environment for high-quality care, teaching, and cutting edge research.
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Our Quality Assurance (QA) department is currently on the hunt for a QA Associate supporting the development, manufacture, and testing of viral vectors for early phase clinical trials. Quality Assurance Associate (Gene Therapy Program.
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Serve as QA lead for quality system elements including Document Control, Training, Deviation Management, Internal and External Inspection, Supplier Management, Risk Management, Complaints, Recalls, etc.
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SageSure, a leader in catastrophe-exposed property insurance, is seeking a Director, Quality Assurance. In this pivotal role, you will ensure the quality of work we deliver to the market, communicate the appropriate quality metrics to stakeholders at various levels, and drive best practices for quality in collaboration with colleagues across the organization while simultaneously leading and managing a team of onshore and offshore professionals.
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The Quality Control Environmental Monitoring Associate I is responsible for performing sampling and testing in support of manufacturing and validation activities, under the direction of a Supervisor or higher.
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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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The Quality Manager is also responsible for clinical privilege development and management of the TUHS Medical Staff Affairs Department, internal Credentialing Verification Organization (CVO) which oversees the credentialing of TUHS physicians and APPs working in non-licensed TUHS facilities.
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The QA Supervisor will provide Quality Assurance support for the Quality Inspectors on the production floor, incoming material quality, and/or distribution quality, including quality oversight for material management of materials at Catalent-Philadelphia.
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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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Interact with MFG management to provide quality perspective on routine operations and support systems. Acts as the Primary Quality Assurance Representative for designated clients. Participate in quality and process improvement initiatives, and project teams.
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Responsible for the product quality lifecycle of respective products within drug delivery (e.g. Change Control, Deviations, Complaints, CAPA.) Provides leadership over the Quality Operations teams that are involved in batch record creation, batch record review, product release, deviation management, change controls, and customer interactions.
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Gathers and manages field quality information (including Technical Reports from field, warranty claims, telematics data, Customer Advocacy Department [CAD] data, web forum information, National Highway Traffic Safety Administration [NHTSA]-Vehicle Owner's Questionnaire [VOQ], etc.
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Join us here at Liberty Coca-Cola Beverages LLC. Summary Quality assurance technicians perform various functions in ensuring quality standards and batching within their company’s production facilities while ensuring the safety of our people, workplace and environment and meeting all company, legal and other requirements.
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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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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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Title: quality Company: Incendia in Philadelphia, PA
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