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Description: The QC Chemist III (internally titled Scientist III, Quality Control) is responsible to perform testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculate and report results on applicable specification documents, participate in method transfer activities within departments or between facilities or organizations.
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The Lead, QC Chemist performs specific routine analysis of samples of raw materials, in process, and finished products according to established (official and/or in-house) test procedures.
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Unload hazardous and non-hazardous raw materials received via rail and truck into storage tanks. Unload packaged hazardous and non-hazardous raw materials into warehouse storage.
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The Quality Control (QC) team is responsible for testing products, raw materials and the manufacturing environment to ensure the Safety, Quality, Identity, Purity and Potency produced by the Catalent Madison Biologics facility.
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The QC Analyst II is responsible of performing incoming raw materials, in-process samples, intermediate products, final products, and stability samples analytical analysis per approved internal and customer specifications following associated procedures to support both product manufacturing and commercial product release.
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The QC Analyst I activities include but are not limited to developing and implementing testing, sampling, and inspection procedures on raw materials, equipment, in-process materials, and/or finished products to ensure that product specifications and company and regulatory requirements are met.
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Perform routine quality control testing on raw materials, process intermediates, and final cell therapy products using established protocols. The Senior Scientist/Associate Director, QC will have both quality control and method validation experience; specifically, experience leading both early phase qualification and late phase validation.
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Knowledge of raw materials, production process, quality control and costs preferred. Reporting to the Operations Manager you will support and supervise the processes and procedures in the plant in order to maximize quality, safety, productivity, and profitability.
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Support bioassay testing for raw materials, drug substance and drug product, including generation of testing data to support clinical studies. Quality Control, Bioassay Associate 1.
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Assess process quality parameters and food safety and quality systems daily, including cross checks, raw materials, calibration, maintenance, procedures, food safety, training, auditing and oversight of analytical testing performed in control rooms.
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Test to positively release incoming bulk and packaged raw materials, such as vegetable oils, lecithin, white mineral oil, and create the related lot numbers and COAs. Complete all other duties as assigned by Quality Control Supervisor/Manager.
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Reporting into the Quality Manager, the Quality Technician position will be based out of our King of Prussia, PA site and will be responsible for performing QC duties of an experienced technician on standard products, intermediates and raw materials, under supervised conditions.
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Make disposition on all raw materials, components and finished products as directed by the Quality Systems Manager. The Quality Systems Supervisor will assist in the direction and maintenance of all daily operations of the Quality Assurance/Quality Control department at a Kleen Test Products location.
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Assist the Quality Systems Manager in the direction of all activities of Quality Department personnel. Assist the Quality Systems Manager as deemed necessary to manage and coordinate the investigation of Out of Specification results for analytical and microbiological tests.
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The Quality Control organization responsibilities include bioanalytical, chemical, microbiological, and in vivo testing of raw materials, in-process materials and finished products.
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raw materials quality control jobs
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