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At least 5 years of QA or Manufacturing experience in a GMP manufacturing environment with a Bachelors Degree in Biology, Chemistry, Chemical engineering, Biomechanical engineering, Bioengineering, Biomedical Engineering, Biochemistry or related field.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Manage the QA communication and lot disposition process with CDMO client base. Perform batch disposition of all GMP materials for release into clinical trials encompassing batch record review, change control and investigation.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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3 years' experience of Quality Assurance oversight of aseptic manufacturing and all production stage batch record review and disposition. Provide training to all QA Associates and Specialists on surveillance oversight and on-the-floor Batch Record review requirements.
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Keywords: GMP, GLP, GXP, GCP, batch record management, batch record review, full-process manufacturing, cell therapy, deviations, junior role, maintenance, calibration, FDA, EMA, biopharmaceuticals, quality assurance, QA.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Specialist, QA Operations, is responsible for quality oversight of Cell Therapy Development Operations (CTDO) activities in accordance with BMS policies, standards, procedures, and Global cGMP requirements.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Performed by Maintenance or outside service providerProper disposition of discrepant machinesEmergent maintenanceAnnual machine calibrations in concert with QA departmentPlanner support related to technical clarity or material estimates as needed:Planning for and ordering the proper type and quantity of weld filler metal as requestedExperience and ability to program procedure driven parameters into applicable welding machines is preferred.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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We are seeking an experienced QA professional to join our QA/C group at the Senior Manager level to perform key batch record review and disposition tasks supporting Ionis clinical products.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Works in accordance with QA Supervisor to provide quality assurance oversight where the business is responsible for adhering to current Good Manufacturing Practices (cGMP) including warehouse, manufacturing processes, inspection, labeling and packaging, batch record review, batch disposition and product distribution as applicable.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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Knowledge and application experience with batch record review, product disposition/release, change control, Apply knowledge of quality processes, including batch record review, material disposition, triaging of deviations.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Specialist, QA Operations, is responsible for quality oversight of Cell Therapy Development Operations (CTDO) activities in accordance with Client policies, standards, procedures, and Global cGMP requirements.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Hands-on experience with batch record review and product disposition is preferred. Hands-on experience with batch record review and product disposition is preferred. Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing.
$29 - $35 an hourFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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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.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Ensures that critical materials used in the manufacture of cellular immunotherapies and gene therapies, are sourced appropriately, received and tested according to approved standards, and provides the disposition of these materials.
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The Supervisor, QA – Batch Disposition is responsible for managing a team within the Batch Disposition group (Quality Assurance) and ensuring timely batch record review and lot disposition to release product within prescribed timelines and in compliance with all applicable regulations.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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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.
$86,400 - $162,000 a yearFull-timeExpandApply NowActive JobUpdated 4 days ago
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