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Previous experience with GMP manufacturing equipment prep, formulation, filling, and visual inspection. Previous experience with Manufacturing Execution Systems (MES) or electronic batch records.
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Work with site leadership team to build subject matter expertise across functions in the areas of compounding, sterilization, and single-use assemblies for filtration and filling, device assembly, and visual inspection.
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Routinely performs tasks in relation to cGMP, ISO, and Quality requirements including, but not limited to: Following basic and/or advanced Standard Operating Instructions, ensuring proper batch segregation, performing quality inspections, filling out paperwork accurately and timely.
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Filling activities in non-controlled areas: tube and bottle manufacturing. We have a contract opportunity for a 3rd Shift Manufacturing Filling Operator in Lombard IL. This is a contract position with a real possibility of going contract to hire.
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Initiate and complete or assign investigations and CAPAs related to Manufacturing departments (Formulation, Equipment Prep, Sterile Filling, Autoclave, Inspection, Packaging, Facilities and Engineering.
$89,100 - $95,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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As the Specialist QA II you will be responsible for shop floor monitoring, clearance, and record review during aspects of parenteral manufacturing which includes, but is not limited to raw material release, compounding, aseptic filling, lyophilization, inspection, labeling, and packaging.
$46,265 - $110,500 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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6) Work with the site leadership team to build subject matter expertise across functions in the areas of compounding, sterilization, and single-use assemblies for filtration and filling, device assembly, and visual inspection.
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In this position, you’ll drive quality execution across the sterile operations including manufacturing, filling, packaging and inspection, and associated non batch specific activities in for both commercial and product development services products.
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Perform Filling activities in non-controlled areas: tube and bottle manufacturing. Perform packaging activities including but not limited to: label generation, visual inspection, heat sealing, and utilizing packaging equipment.
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Responsible for performing assembly and packaging operations and assisting in visual inspection/filling operations, if required. All events are to be recorded in the batch record and brought to the attention of the production supervisor for further action.
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Author Batch Records and Specification sheets for Formulation, Filling, Inspection and Finishing. Operational knowledge of Cytiva/Vanrx SA25 or other robotic filling isolator is a plus.
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Will perform a variety of processing duties according to the Batch Production Records (BPRs) and Standard Operation Procedures (SOPs) in the Manufacturing Department including, but not limited to the cleaning / recovery of classified area and workspaces, components preparation, weighing of the raw materials, compounding/formulation, filtration of solutions, aseptic filling, inspection, labeling and packaging.
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Maintains and adheres to safe work habits and all applicable PCI safety procedures and guidelines Demonstrates general knowledge of aseptic techniques Prepares solutions, aseptic filling and labeling of vials under sterile and non-sterile conditions, routine solution and filtration, vial and component preparation and sterilization Assembles, disassembles and operates aseptic filling equipment and lyophilizer equipment in classified cleanroom and controlled non classified environments.
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Calculates percent defective on inspection results and reconciles components on batch record. Job SummaryResponsible for visually inspecting filled product off the filling line following Standard Operating Procedures (SOP) and current Good Manufacturing Processes (cGMP.
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The client is a world leading manufacturer of Medical Diagnostic Devices to test for infectious diseases. Knowledge of good Manufacturing practices (GMP) a plus. Visit to contact us if you are an individual with a disability and require accommodation in the application process.
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filling inspection batch jobs
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