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6+ years cGMP experience in biologics, pharmaceutical and/or vaccine manufacturing operations, including experience in cell culture, recovery, purification, and bulk formulation. Coordinate daily operations and lead on the floor manufacturing employees to complete production activities safely and compliantly in accordance with OSHA and cGMP guidelines.
Full-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Strong knowledge of regulatory requirements and guidelines (e.g., cGMP, GLP, ICH) governing pharmaceutical manufacturing and testing. Overview : The QA/QC Analyst at AstraZeneca is likely responsible for ensuring the quality and compliance of products and processes within the company's pharmaceutical manufacturing or research facilities.
TemporaryExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Chromatography, depth filtration, TFF, cGMP. Experience in manufacturing and cGMP environment. Knowledge of end to end biopharmaceutical manufacturing from upstream processing to fill finish, specialization in downstream processes such as chromatography, depth filtration, TFF, and sterile filtration is highly preferred.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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This position is responsible for performing activities to support analytical testing programs to ensure compliance with cGMP standards including in-process, product release and stability testing.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The role requires knowledge and experience of scientific concepts, practices, and procedures within the biopharmaceutical field and a cGMP environment. Scientist I: Bachelor of Science (MS preferred) in a Life Sciences discipline with 1-3 years of relevant experience working in a Quality Control work environment, preferably in the pharmaceutical industry with knowledge of cGMP is a plus.
$26 - $36 an hourExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Experience with cGMP and/or ISO certification highly preferred. Contribute to process improvement, assay and process development for manufacturing. o Experience with MRP/ERP and JDE systems preferred.
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Job responsibilities include supporting the QE Director in site Technical Operations (TechOps) processes related to cGMP such as Commissioning, Qualification and Validation (CQV), Computer System Configuration Management and Computer System Validation (CSV.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Experience with MRP/ERP and JDE systems preferred. This may include the production of coated plates, chemical buffers, and biological diluents/reagents and/or assembled kits for customer order fulfillment.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Assess client Requests for Proposals (RFP), participate in technical and strategic RFP discussions with the client, and design a technical scope of work for mRNA and/or LNP process development and cGMP manufacturing to support customer strategy.
$129,000 - $193,000 a yearFull-timeRemoteExpandApply NowActive JobUpdated 20 days ago - UpvoteDownvoteShare Job
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We are seeking an Associate Scientist to join our Downstream Process Development group in Gaithersburg, MD. Qualified individuals will be responsible for hands-on execution of downstream chromatography and filtration processes in support of process development, scale-up, process characterization activities, and technical support of cGMP manufacturing for proteins, nanoparticles, and virus-like particle (VLP) based vaccines.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Bachelors degree ORAssociates degree/High School Diploma or equivalent with relevant cGMP experience. As Gene Therapy Manufacturing Supervisor, you will play a critical role in helping to establish REGENXBIOs first internal GMP BDS and FDP clinical and commercial AAV gene therapy manufacturing capability.
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Considerable expertise relevant to QC analytical methods used for cell therapy manufacturing including qPCR/dPCR, ELISA, flow cytometry or cell-based assays in a GMP environment. The QC Scientist will focus on supporting the routine operation of the GMP facility in analytical development, batch release, and stability studies, etc.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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To accomplish this, we continue to be deeply rooted in science and academic research while also having built a fully integrated, global immunotherapy company with cGMP and GMP manufacturing facilities anchored around deep expertise in immunology and complemented by an expanding set of capabilities.
InternExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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1-3 years of relevant experience working in a Quality Control work environment, preferably in the pharmaceutical industry with knowledge of cGMP is a plus. We operate a state-of-the-art facility in Rockville, Maryland with five GMP suites in order to augment its global research and development capabilities and to support clinical development of multiple cell therapy platform technologies in the US.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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This position responsible for supporting the site Technical Operations (TechOps) processes related to cGMP such as Commissioning, Qualification and Validation (CQV), Computer System Configuration Management and Computer System Validation (CSV.
Full-timeExpandApply NowActive JobUpdated 7 days ago
cgmp job in Gaithersburg, MD
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