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Tasks include prepare dosage medications for dispensing into bottles/containers and unit dose packaging/repackaging, counting pills/tablets, mixing medications that need to be reconstituted with water, preparation of oral syringes, compounding sterile preparations, filing, inventory, medication delivery to patient care units, filling/replenishing automated dispensing cabinets, and the collection, organization, and verification of patient information.
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Monitor the pasteurizing, separating, cooling or freezing, filling, mixing, clean-up, standardizing and storing operations to ensure that plant production and quality standards are met. Since 1914, Kemps has provided families with fresh, delicious dairy products, fresh milk, frozen yogurt, sour cream, cottage cheese and frozen novelty treats.
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Solid understanding of the various unit operations of aseptic manufacturing such as bulk freeze thaw, compounding/mixing, filtration, filling and lyophilization for liquid and lyophilized products.
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Engineering principles applied to the manufacturing process including mixing, coating, die-cutting, pouching, and filling processes. or food, or cosmetic manufacturing environment, or an equivalent combination of training and experience.
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In greenhouse, the work involves planting, maintaining and harvesting plants, collecting material for experiments, making crosses, mixing soil, filling pots, cleaning greenhouse. Greenhouse work: plant maintenance, keeping greenhouse organized and clean, seed harvest, washing pots, filling pots, planting seeds, transplanting seedlings.
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Must perform a diverse range of tasks related to operating a variety of manufacturing equipment utilized in the production of various products (i.e. opening, closing, mixing, filling, loading, inserting parts, capping products, tightening lids, sealing bags, etc.
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Knowledgeable in food product manufacturing including thermal process requirements, ingredient handling systems, control systems, CIP, heat and mass transfer, drying, dry mixing, pneumatic product transport, filling, packaging and validation procedures preferred.
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Plant Care: Employee will assist with activities on site that consist of filling pots operating a Pot Filler, Mixing soils, fertilizer, peat moss and other materials, Cleaning Pressure washing, Painting.
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Typical processes being developed / validated include mixing, filling, formulation, visual inspection and lyophilization. 5-7 years in Process Validation (formulation, filling, visual inspection and/or lyophilization.
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Consults and interacts with internal cross-functional teams and external clients and customers Operate equipment and apply analytical methodology utilized in the formulation development of parenteral dosage forms ( lyophilizers, compounding/filling equipment, mixing techniques, sterilization techniques, HPLC, KF, particulate matter, etc.
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Background in a wide variety of manufacturing processes and techniques, including material handling systems, mixing systems, gravimetric/volumetric filling systems, autoclave/sterilization techniques, robotic handling and assembly workcells, and industrial drying techniques.
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Apply fundamental engineering principles to the design, development, scale-up, and validation of processes for sterile drug product unit operations (e.g., refrigerated/frozen storage and handling of bulk solutions, dissolution of APIs, pooling and mixing, sterile filtration, filling, pre-filled syringe processing, lyophilization, and vial capping) for both small molecule and large molecule parenterals.
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Experience in applying fundamental engineering and scientific principles to the characterization of freeze/thaw, formulation/mixing, filtration, filling, lyophilization, capping, and visual inspection.
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Experience with Drug Substance and Drug Product Equipment (Aseptic Filling Lines, Visual Inspection Machines, Label/Pack Lines, Ultrafiltration, Chromatography, Mixing Skids, Single Use Mixers, Buffer Prep Vessels, Temperature Control Units, Clean in Place Skids, etc.
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Acts as single Point of Contact (POC) to drug product teams to provide expertise/knowledge of manufacturing site process capabilities and practices in drug substance freezing/thawing, formulation, filling vials/syringes/devices, lyophilization and visual inspection.
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