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Perform batch disposition of all GMP materials for release into clinical trials encompassing batch record review, change control and investigation. Prior experience with batch record review and releasing batches.
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DPS Group is seeking a qualified Senior Quality Assurance Operations professional to perform batch disposition, batch record review, deviation, CAPA and change control support at the Norwood, MA client site.
Full-timeExpandApply NowActive JobUpdated 7 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. Full lifecycle review and disposition of parenteral manufacturing Batch Records (Formulation, Filling, Inspection, & Packaging) for Media Fills and Drug Product.
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Supports disposition activities for manufactured products in support of Commercial/Clinical Product, including Master Batch Record review, Executed Batch Record review, resolution of comments/issues and Certificate of Analysis review.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Understanding cell culture, cryopreservation, purification, aseptic processing or lab technique, Packaging, Shop floor quality, batch review, or disposition preferred. Working knowledge of Electronic Batch Records (EBR), Review by Exception (RBE), and MES Recipe object lifecycle management preferred.
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Familiarity with MES infrastructure, HP ALM, Electronic Document Management Systems, Change Management Systems, and middleware WebMethods preferred. If you are ready to challenge yourself, accelerate your career, and give new hope to patients, theres no better place than here at BMS with our Cell Therapy team.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Hands-on experience with batch record review and product disposition is preferred. 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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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.
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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 18 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 1 month ago - UpvoteDownvoteShare Job
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Key Duties and Responsibilities Oversee - all aspects of external (CMDO) quality control operations including specifications, stability, data review, investigations, batch disposition, and analytical method qualification and validation.
ExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Experience in FDA/EMA regulations in biopharmaceuticals or cell therapy manufacturing. This is a second shift/night time opportunity. Piper Companies is currently seeking a Environmental Monitoring Associate based in Durham, North Carolina for work at a leading pharmaceutical company.
$29 - $35 an hourFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Traitement des alertes techniques - Traitement des incidents - Prise en charge des livraison des composants Techniques - Surveillance du stockage - Surveillance de l’espace disque (dont batch techniques associés) - Assistance Technique Editique & Output Manager - Administration des Traitements techniques EOS et OUTPUT MANAGER - Evolutions (Industrialisation incluse, JCL, REXX.
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Ensuring accurate and timely review, as well as maintaining, clinical manufacturing GMP/batch related. " Perform Real time review /approval of executed batch records and Chain of Identity verification.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Conducts record review of executed batch records, QC testing data, and associated batch file documentation to ensure timely disposition of patient lots. The Sr. Quality Assurance Specialist will be responsible for supporting quality functions such as line clearance, batch record review, label issuance, raw material release and facilitating timely release of production lots.
ExpandApply NowActive JobUpdated 4 days ago
disposition batch jobs
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