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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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The primary function of a method development/validation chemist is to support analytical chemistry method development and validation projects for raw materials including Active Pharmaceutical Ingredient (API) and finished products.
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The Weigh and Dispense Associate position is responsible with assisting and executing in the set-up, and weighing of raw materials, solvents, and solutions used in GMP manufacturing at FDBN. This role will interact with manufacturing personnel in both Drug Substance and Drug Product teams as well as Warehouse for commercial operations and tech transfer activities required from the Weigh and Dispense operations.
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Manages Raw Materials and Component inventory to ensure maximum up-time of manufacturing within IOS and amongst CMO and other partners. They are responsible for operations involving Material and Component Planning, Materials Logistics, and Inventory Management in a cGMP environment.
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The Materials Technician receives, ships, stores and distributes raw materials, intermediate and marketed products in compliance with cGMP and company SOPs. Ship materials as requested using any of the major carriers: FedEx, UPS, DHL or US Mail.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The Position encompasses 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.
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This position will focus heavily on utilizing analytical instrumentation, stability testing of raw materials and drug products, as well as other tasks as assigned. Performing in-process, Release and Stability testing of Raw materials and Drug products.
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Job Summary: Performs a variety of chemical analyses and GMP review of raw materials, packaging components, ancillary solutions, in-process samples, finished product and stability samples in accordance with cGMP, GLP, DEA and company policies and procedures.
$34ExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Conduct critical chemical and physical analysis on raw materials, initial, in-process and final products, and samples collected from the environmental monitoring programs at the Round Lake manufacturing facility.
$25 - $30 an hourExpandApply NowActive JobUpdated 4 months ago - UpvoteDownvoteShare Job
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Coordinates the ordering of raw materials used in the production processes with Materials Management. This individual exhibits model behaviors in accordance with environmental, health, safety, and cGMP guidelines.
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Lead the design and execution of studies to qualify new components and raw materials for use in cGMP manufacture. Lead the design and execution of process optimization studies for cGMP manufacture.
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Our products are derived from renewable raw materials found in nature for use in jam, fruit and milk drinks, confectionery products as well as industrial applications. We work across the whole value chain from natural raw materials to customers’ end products.
$80,000 - $106,000 a yearFull-timeExpandApply NowActive JobUpdated 14 days ago - UpvoteDownvoteShare Job
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Operate expansion and production reactors, conduct harvest operations, and order and account for consumption of raw materials and components. Operate bioprocess equipment under strict adherence to cGMP, OSHA and required policies and regulations.
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This position requires working collaboratively with the QC raw materials, QC Analytical, QC Microbiology, Quality Assurance and Manufacturing groups. The incumbent in this position will ensure Instrument validation activities are performed and maintained in a safe and cGMP compliant work environment and comply with company policies and regulatory/industry standards.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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The Lab Technician working in the stability lab will timely analyze and / or test under cGMP and as per the Quality Department SOPs and Specifications, a variety of materials including API (Active Pharmaceutical Ingredients), raw materials, intermediates and finished products for Nutritional Supplements applying validated or compendia methods for the stability testing.
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