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Analysis of silicone raw materials, intermediate formulation mixes and final formulations using various state-of-the-art analytical techniques including but not limited to GPC, HPLC, GC, rheometer, UV-vis and others.
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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 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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External US Key responsibilities for this role include:Responsible for testing and approving raw materials, intermediates, and final products following company processes and procedures via use of lab equipment (eg: GC, Karl Fischer titration, ICP-MS, NVR.
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Routine analysis and evaluation of raw materials and products at all stages of the development process under stringent quality and time requirements with GC, HPLC, GCMS, or NMR. GC, analytical chemistry, wet chemistry, batching, sample preparation.
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Iovance is seeking an Analyst II, Quality Control (QC) Raw Materials, who will be responsible for the sampling, release testing, data review, and vendor qualification, for all raw material lots received for use in the manufacturing of product at the Iovance iCTC site.
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Author Standard Operating Procedures for new instruments/software Perform routine testing to support the release of finished product, raw materials, API Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.
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The role of QC Biochemist/Analytical Chemist II is responsible for supporting the operations and manufacturing process by performing routine and non-routine analytical testing raw materials, in-process, finished formulations, stability samples, method development and/or transfers, and cleaning validations.
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The Quality Lab Associate I will be located at the Drug Delivery Chemistry Laboratories, Round Lake, IL. The Position encompasses the biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) through all stages of the manufacturing process from incoming raw materials to finished goods, and environmental monitoring programs.
$28 - $32 an hourFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The Chemist II, under general supervision, performs QC laboratory chemical analyses of raw materials, in-process materials, stability, and finished products, and testing to support process validation.
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The candidate will interface with MFG team to perform failure analysis at different stages of modulator manufacturing and the Nematic Curvilinear Aligned Phases (NCAP) and will be responsible in qualifying new raw materials and understand the complex interaction between cross-linkers, polymers, defoamers to produce consistent polymer-liquid crystal devices.
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Responsible for sampling incoming raw materials for analysis, including lifting 50lbs repeatedly. Perform daily testing of all raw materials, intermediates, and finished products.
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QC Chemist Perform release, stability and special request testing of finished products and raw materials following Standard Operating Procedures (SOPs), in-house test methods, and/or compendial methods.
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Perform assigned sampling, physical, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemicals, physical and instrumental techniques (HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments) as per as per USP monograph / In-house / any other Compendial monographs.
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The Quality Control Analyst is an integral part of the CURIA team, contributing to our success by testing raw materials, intermediates, finished goods and bulk pharmaceuticals, as well as in-process production testing in compliance with the requirements of CURIA. The QC Analyst is expected to provide fast, accurate and efficient analytical support to the department's customers, both internal and external.
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