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Performs analytical testing of raw materials, finished products, and in-process samples within a cGMP/cGLP environment utilizing instrumentation (HPLC, GC, ICP, FTIR, UV) and wet chemistry.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Review and disposition of incoming raw materials. Some working knowledge of quality systems cGMP standards applicable to clinical biologics DS and DP. Some working knowledge of quality systems cGMP standards applicable to clinical biologics DS and DP.
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As the Analytical Laboratory Supervisor, you hold a pivotal position in conducting essential testing for raw materials, finished bulk products, and third-party product releases. Assign work tasks and ensure timely completion and release of raw materials, bulk products, and third-party products.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Counts physical inventory of all raw materials and finished goods in the warehouses and coolers. Work with the department Associate Team Leaders and Team Leaders to ensure compliance with all cGMP, ISO and FDA guidelines for warehouse activities.
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The QC Analyst will set up and execute daily testing of final API product and raw materials. Sample raw materials per the material specifications and perform in-house testing.
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We work in the local plant connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products. Experience Required: •Capable of working alone, and managing work loaded that is directed •Computer skills are required, should be proficient in standard laboratory techniques and laboratory data management systems Preferred Skills: •Lab data management systems •Microbiology and aseptic technique is advantageous and raining will be provided •cGMP •Previous laboratory work •Proficient in standard laboratory techniques and laboratory data management systems.
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They support the production groups by ensuring the suites are appropriately stocked with raw materials and consumables, assemble and autoclave assemblies for use, clean soiled parts, perform daily/weekly maintenance on analytical equipment, and complete scheduled cleaning requirements that are not fulfilled by Client’s contracted cleaning staff.
Full-timeExpandApply NowActive JobUpdated 12 days ago - UpvoteDownvoteShare Job
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The QC Associate Operations position is responsible for executing sample management activities, which include control, receipt, and distribution of product, intermediates, raw materials samples, sample retention, reference samples, and stability samples at Fujifilm Diosynth Biotechnologies California (FDBC.
$30 - $34 an hourTemporaryExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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As the Senior Manager, R&D Team Leader you will be required to have knowledge, experience and skills to manage an analytical group for an AR laboratory operation in a solid controlled release dosage pharmaceutical team, focusing on instrument/equipment validation/qualification and repair supporting release testing, raw materials testing, in process testing for finished products and the corresponding lab investigations.
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HPLC Wet Chemistry GMP Performs microbiological or analytical chemistry examination testing on raw materials, finished products, environmental monitoring (air, water, surface) and stability samples in accordance with approved Standard Operating Procedures (SOPs) or USP methods, where applicable.
$38 - $43 an hourExpandApply NowActive JobUpdated 24 days ago - UpvoteDownvoteShare Job
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This includes, but is not limited to; production, testing and disposition of Biological Drug Substance (BDS) or Antibody Drug Intermediate (ADI), raw materials and cell banks at. Provide quality oversight to internal/external organizations for the manufacture and analysis of BDS or ADI, raw materials, cell banks and critical.
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Perform chemical, physical and microbiological tests of raw materials in progress and final product. Responsible for performing routine release testing for finished goods and raw materials.
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Accurately weighing raw materials and active ingredients and combining them into a blend. Participates in the completion of work orders, including batch record documentation per cGMP (current good manufacturing process.
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This role is responsible for maintaining adequate inventory levels, stocking the production supply rooms, processing incoming raw materials, managing materials in the ERP system, and completing annual physical inventories.
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Perform a large variety of routine and complex analytical procedures in the analysis of pharmaceutical products and raw materials by various testing techniques including but not limited to Wet Chemistry, GC, HPLC, UV-Vis, FTIR, ICP, GFAA and Dissolution etc.
ExpandApply NowActive JobUpdated 30 days ago
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