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Performs batch record review, EWI (Electronic Work Instruction) revisions, and work order generation. Demonstrates general knowledge of automation systems (INFOR, MES, ERP, DeltaV.
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Minimum of [X] years of experience in batch record review within a pharmaceutical or biotech manufacturing environment. Contribute to continuous improvement initiatives to enhance batch record review processes and efficiency.
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The Supervisor will provide overall Quality Assurance support inclusive of but not limited to review and approval of room qualification protocols/reports, line clearance, ongoing environmental monitoring/ cleaning documentation, APV’s / PPQ’s, routine production, batch record review and release of iPBMCs∯*∯ The successful candidate will support and manage the internal team and be on site.
Full-timeExpandApply 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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Hands-on experience with batch record review and product disposition is preferred. Ensure that all required documents are accurate, including all batch related deviations. Piper Companies is currently seeking a QA Specialist based in Fort Washington, Pennsylvania for work at a leading consumer testing company.
Full-timeExpandApply NowActive JobUpdated 19 days ago - UpvoteDownvoteShare Job
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Field QA Specialist is responsible for quality activities for the Single Use Facility in accordance with Client policies, standards, procedures, and Global cGMP. Functional responsibilities include ensuring manufacturing compliance with applicable procedures and batch records, providing real time review of manufacturing batch record documentation and logbooks, and working with operations to resolve manufacturing issues.
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Maintains current database records related to batch record review, storage, and archival. Coordinate the storage and retrieval of all batch records from the batch record archives.
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You have previous QA operations experience, particularly with batch record review / MES design, implementation or training. Review and approval of documents including executed Batch Records and SOPs (electronic and paper-based.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Duties include purposeful presence on the shop floor, electronic batch record creation, batch record review, SOP revision approval, work order approval, and quality approval of minor deviations and CAPA records.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Strong experience with executed batch record review and in-depth knowledge of quality and regulatory requirements for the disposition of pharmaceutical products. Perform review of batch records and test data and perform product dispositions.
$175,000 - $207,000 a yearExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Quality Assurance support areas include but are not limited to Batch Record Review, Product Release, Standard Operating Procedures, Investigations, CAPA, Change Control, Shop Floor Audits.
$24.2 - $29.2 an hourExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Performs activities for manufacturing (i.e., batch record review, packaging line clearances and manufacturing room clearances, deviations, etc. Perform in-process testing and inspections as required by Master Batch Record (weighing, visual inspection etc.
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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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The Quality Controls Manager will monitor and control the daily activities of quality inspections of incoming, in-process, final, and batch record review and release. Schedule and prioritize quality inspection, testing, and batch record review and release to support Operations and release of product.
$100,000 - $125,000 a yearFull-timeExpandApply NowActive JobUpdated 15 days ago - UpvoteDownvoteShare Job
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Specific responsibilities include but are not limited to Quality support/oversight and leading initiatives related to: tech transfer and facility start-up, floor operations, QMS record review, MBR and SOP generation/revision, training, materials management, equipment management, and maintenance at the Editas Waltham and Editas Devens GMP manufacturing facilities.
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