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Keywords: clinical supplies, biologics, vaccines, electronic batch record review, batch record, cGMP, SOPs, specifications, labeling, regulatory submissions, SAP, Trackwise, Midas, Veeva, QMAS, QA, Quality Assurance.
Full-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Manager will be looking for the following skills: cGMP experience / Clean room experience / 5yrs minimum within the pharma industry - NO FOOD INDUSTRY / Deviation Management experience / Technical skillsets - (engineering, etc) / Extensive documentation experience (not batch record review - not a good fit) / Validation experience - good fit.
ExpandApply NowActive JobUpdated 1 month ago - 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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Complete production batch record review (post- Production) Perform a thorough review of batch records and related GMP documentation, identifying and resolving discrepancies in a timely manner and implementing corrective actions to improve the batch record execution/review process.
Full-timeExpandApply NowActive JobUpdated 10 days 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 18 days ago - UpvoteDownvoteShare Job
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Familiarity with manufacturing batch records is a key skill necessary for success in this position; prior batch record experience is a strong plus. Familiarity with computer systems (SAP, LIMS, electronic batch records) is a plus.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Will review Batch Records. Must have GDP review experience. The position will interact with other departments including Manufacturing, Packaging, Quality Laboratories, Quality Systems, Validation, Engineering, Maintenance and other departments as it relates to site Quality Assurance responsibilities.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Perform QA tasks related to the manufacturing of diagnostic test kits including batch record review, packaging/finished product forms, and additional required documentation. biology, batch record review, quality assurance.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The position is responsible for providing daily Quality Assurance support to the manufacturing site to ensure internal and regulatory cGMP and CFR requirements are met. SAP and LIMS is helpful. cGMP/ GDP/ Pharma Quality Analyst (ONSITE.
ExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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GMP, Batch records. GMP, Batch records. Must have cGMP exp. Communication Skills, Knowledge in Automation and Previous Experience in a similar position. What would you consider to be the top 3, non-negotiable skills that you will be looking for hen reviewing candidate resumes.
ExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Quality Assurance Associate, QA, Pharmaceutical, West Point, PA, Pennsylvania, FDA, GMP, Batch Record, Manufacturing, GDP, cGMP, Batch Records, Regulatory Review, Comprehensive Benefits Package, Health, Vision, Dental, #LI-ONSITE #LI-DF #Pando.
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