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Provide training to all QA Associates and Specialists on surveillance oversight and on-the-floor Batch Record review requirements. Senior QA Specialist - Batch Review.
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Performs audits of manufacturing and support areas, including in-process batch record review for adherence to internal procedures and Good Documentation Practices. This leadership role is primarily responsible for adherence to defined timelines as it relates to the development, support and executions of programs/governing procedures including Quality on-the-floor oversight of manufacturing activities, batch review, deviations, CAPAs, and change controls.
$125,000 - $186,000 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Ideal candidates will be local, with 8+ years of relevant experience supporting Batch Record Review and Product Disposition. Strong background in Batch Record Review experience required.
ExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Perform batch record review and release for finished product, raw materials, intermediate solutions, and services. Experience working in a Quality Department/Life Sciences-Regulated environment, including experience independently conducting internal audits, document review from a technical and quality perspective, batch release, incoming inspection.
$75,000 - $110,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Performs SAP transactions required to document Batch Record review. Batch record review experience. Looking for GMP/PHARMA/BIO-PHARMA profiles with batch record documentation experience.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Manage the Product Release Program, batch record review process, metrics, and customer CofAs. As the Quality Systems Manager, you will play a pivotal role in championing daily activities for quality excellence.
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Quality Control, Documentation, Sciences, Batch Record Review, GMP, Biology, IQ, PQ, FATs, SATs, Cleaning validation, equipment calibration, pharmaceutical. Quality Control, Documentation, Sciences, Batch Record Review, GMP, Biology, IQ, PQ, FATs, SATs, Cleaning validation, equipment calibration, pharmaceutical.
$25 - $30 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Apply knowledge of quality processes, including batch record review, material disposition, triaging of deviations, investigations, CAPA, risk management, change control, and product complaints.
$36 - $39 an hourExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Perform batch record review on daily quality control line paperwork. GMS and QMS site leader. Perform batch record review on daily quality control line paperwork. Pharmaceutical packaging experience is a plus.
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Manage all aspects of a cGMP manufacturing campaign, including batch record review, safety evaluations, material procurement, equipment ordering/set up/cleaning and execution of the chemical operations.
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Completes batch record review at the final stage of the manufacturing process with minimal assistance and approves their final release once it has been determined that all compliance and procedural requirements have been met.
$33 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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There are over different products/SKUs and ingredients, so there will be a lot of details to learn and pay attention to as far as labels, codes, packaging, lot numbers and batch record review.
$25 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Location/Division Specific Information St. Louis MO / Pharma Services Group This is a non-supervisory role, reporting to the QA Supervisor Batch Record Review and Release at the Thermo Fisher St. Louis site.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Production, Gmp, Cleanroom, Packaging, batch record review, sop, General labor, General production, mathematics. Team members executive a variety of simple and complex tasks per written procedures, Batch Records and GMP processes which may include handling of controlled substances and potent drugs.
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Batch Record Review of drug substance. Review of QC Analytical and Microbiological data. Active participation at the Deviation Review Board, Site Quality Council and other relevant forums pertinent to product quality review.
ExpandApply NowActive JobUpdated 14 days ago
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