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Handles Return Material Authorization (RMA) process to include tracking, contacting (internal) customers regarding returns, metric reporting, disposition with QA and coordinating with freight companies.
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Performs QA / QC procedures as assigned. Investigates specimen status and report disposition. Responsibilities: All duties of a Specimen Processor including:- Answers phone inquiries.
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Contribute to process improvement of batch records and turnaround times to ensure turnaround times and QA batch disposition deadlines. Legend Biotech is seeking QA Batch Disposition Specialist as part of the Quality team based in Raritan, NJ.
Full-timeExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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The QA Reviewer is responsible for a variety of Quality activities to ensure compliance with applicable quality objectives and regulatory requirements in the cGMP Quality organization. Thorough knowledge of and competence in quality processes, including but not limited to material disposition, deviations, investigations, and CAPA management.
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Closely partner with QA peers for rapid disposition of mRNA. This role involves actively participating in a collaborative team to execute manufacturing operations using disposable technologies and automation, adhering strictly to cGMPs and standard operating procedures, while demonstrating a keen understanding of bioprocess unit operations and contributing to the production of GMP mRNbased medicines for human clinical trials.
$31 - $33 an hourFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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This includes developing QA specific procedures related to product disposition, line clearance and review and approval of GMP documentation including but not limited to Batch Records, Validation Protocols/Reports, and Calibration/Work Order Records and new equipment enrollment.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Liaison between other QA co-packer staff and QA staff members in determining acceptability and disposition of subpar product. Must be able to work independently, manage multiple priorities, and interact with different plant members as well as QA staff.
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You'll complete QA processes including batch record review, sampling and inspection of incoming materials, product disposition and quality issue resolution to maintain the flow of products and documents to meet site objectives.
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Provide day-to-day support and guidance on control testing, including participating in walkthrough meetings, reviewing documentation and assessing the adequacy, and leading final disposition meetings.
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The QA Technician provides direct quality support to the production area. Handling of nonconformities (NCR), including root cause analysis, corrective & preventive actions, e.g. rework/repair, or disposition decisions (Scrap, Release to Customer, Return to Stock.
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The QA Manager may also support calibration and validation document reviews when necessary. The QA Manager role is a key leadership role responsible for leading a team of QA specialists to ensure products are delivered on time and to drive continuous improvement.
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Those functions may include but is not limited to the oversight and approval of laboratory protocols and reports, data review, batch record review, deviations, product complaints, change controls, and CAPAs using the quality management system.
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The Senior Specialist of Quality Assurance (QA) Lot Disposition is a full-time position located at the BMS Cell Therapy Manufacturing Plant (Jump) in Bothell, WA. The primary focus for this role is to ensure final drug products and incoming raw materials are released to market following all internal procedures and cGMP requirements.
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Hands-on experience with batch record review and product disposition is preferred. The primary focus of the QA Associate role is to support commercial production to ensure consistent compliance with regulatory and industry expectations.
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After QA representative and Manufacturing Engineer do MRB each week, they give the blue copy of the tickets to the Material Handlers and they process the transfer from RJ-WIP to RJ or scraps the parts depending on the disposition of the parts and take the blue tickets to Leah Bailey in QA. The parts are then moved to RJ in receiving or the dispositioned location on the ticket.
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