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Experience with GMP quality systems, including document management, change control, deviations, and CAPA. Strong analytical and problem-solving skills, with the ability to interpret and apply complex regulatory requirements.
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Direct knowledge of design and troubleshooting with GMP Biopharmaceutical Production facility equipment/systems such as cell culture reactors, chromatography, filtration, as well as other equipment needed to support these processes such as autoclaves, clean in place (CIP) systems, washers, clean steam, etc.
$43 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Keywords: Chemistry, Chemist, HPLC, GC, Gas Chromatography, Mass Spectrometry, Karl Fischer, cGMP, GMP, GLP, LIMS, Laboratory Technician, Quality Control, Pharmaceutical, SCM, pH, Dissolution, Disintegration, Compendial, Method Transfer, Method Verification, Method Validation, Quality Control, We Chemistry Analytical Technique, Analytical Equipment.
$71,000 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Work under the Production Department director to support production by performing GMP radiochemistry processes in a safe, efficient and timely manner. Maintain physical inventory of all material assigned to GMP Suites.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Direct knowledge of design and troubleshooting with GMP Biopharmaceutical Production facility equipment/systems such as filling, isolators, lyophilization, cappers, inspection as well as other equipment and utilities needed to support these processes such as autoclaves, clean in place (CIP) systems, washers, tunnels, clean steam, water for injection, etc.
$138,188 a yearFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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We offer extensive facilities including PET/MRI, PET/CT, SPECT/CT, multiple medical cyclotrons, and GMP radiopharmaceutical preparation supporting cutting-edge clinical care and translational research.
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Establish and manage production department KPI’s related to performance and throughput of GMP radiopharmaceutical operations. The Director of Production will set vision and drive a culture of compliance and teamwork in a GMP radiopharmaceutical environment.
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Key Placement Activities Experience of key analytical techniques and processes, aligned to the characterisation of drug substances or pharmaceutical dosage forms, including HPLC, GC, dissolution, MS, NMR, vibrational spectroscopy, Karl-Fisher, automated methods and platforms, method validation, stability testing, batch analysis testing and documentation, performed in environments compliant with Good Manufacturing Practices (GMP.
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Complete and comply with the Master Sanitation Schedule (MSS), Daily Routine List (DRL), HACCP procedures, Good Manufacturing Practices (GMP), Integrated Pest Management (IPM) compliance. The company’s portfolio includes beloved brands such as Honey Bunches of Oats®, PEBBLES®, Grape-Nuts® and Malt-O-Meal® cereal, and Peter Pan® peanut butter, as well as Rachael Ray® Nutrish®, Kibbles ‘n Bits® and 9Lives® dog and cat food.
Full-timeExpandApply NowActive JobUpdated 13 days ago - UpvoteDownvoteShare Job
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Organize process auditing and process auditing controls to bring visibility to PM quality, time allocation of maintenance resources, cost control, and adherence to safety and GMP standardsPossess a high degree of initiative and flexibility to meet commissioning and operational needs post-commissioningPerform additional assignments made by the corporate engineering team / Site Director.
$120,880 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Analytical Development (AD) / Quality Control (QC) team at the Center for Bioinnovation and Manufacturing (CBM) seeks an AD/Quality Control Associate II (QCA II) to support in-process and release testing for GMP Manufacturing and analytical development of gene and cellular immunotherapy products.
$32 - $48.82 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Direct the efficient maintenance and improvement, installation, and safe operation of food processing equipment in compliance with company, State, and Federal policies; procedures, and regulations including OSHA, FDA, SQF, AIB, EPA, GMP, NFPA, NEC and other code and regulatory agencies.
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RadioMedix Inc., a biotechnology company located in Humble, Texas, is looking for an experienced Manufacturing Associate to work at its newly constructed GMP radiopharmaceutical manufacturing facility.
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The Manufacturing Associate is responsible for execution of manufacturing processes within a GMP-compliant facility specializing in cell and gene therapy production at AmplifyBio’s Manufacturing Enablement Center ( AMEC ) Facility.
Full-timeExpandApply NowActive JobUpdated 30 days ago - UpvoteDownvoteShare Job
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Manages the Maintenance Supervisors, Maintenance Planner/Scheduler, Storeroom Clerk, and the MRO Purchaser. Drives Plant asset integrity and reliability program, including proactive maintenance programs, such as predictive maintenance programs, Total Productive Maintenance (TPM), maintenance scheduling, root cause analysis, improvement through Lean Six Sigma techniques and other best practices.
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gmp job Company: Genoskin
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