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The site features inhaled powder spray drying, as well as multiple commercial-scale lines for capsule filling and blister packaging. On-site spray dryers include best-in-class GEA Niro SD1, SD4 and SD7, the latter being the largest CGMP unit of its kind for DPI in North America.
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This position is responsible for performing operations related to the manufacturing and/or packaging of pharmaceutical products through equipment set-up, operation, clean-up and maintenance in compliance with all regulatory cGMP requirements and company policies and procedures.
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Assist in the bulking/filtration process prior to aseptic filling. Perform facility cleaning of critical aseptic environment as required to maintain a cGMP environment and in accordance with Standard Operating Procedures.
$19.36 an hourExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Provides services for the prompt and accurate filling, packing, and shipping of customer orders. Knowledge of cGMP requirements as it pertains to FDARP as applicable to the facility. Assuring quality of blended products, accuracy of weight/quantity of repackaged products, accuracy and promptness of filling orders, cleanliness of warehouse and product.
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Operate and maintain highly automated bottle handling, filling, vision inspection, conveying, or process batching equipment in a cGMP compliant manner, using HMI/SCADA interfaces. The Line 4 Technical Lead position is responsible for front line troubleshooting, process improvement oversight / execution, basic to intermediate maintenance, and as needed operation of high speed equipment used in the production of BacT/ALERT bottles in a cGMP compliant manner.
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Knowledge of cGMP for pharmaceutical and/or vaccine manufacturing, Lean Six Sigma Methodology, Root Cause Analysis, Failure Mode Effects Analysis, knowledge in reliability engineering (including asset life cycle management.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Understanding of cGMP, SOPs, and regulatory requirements in pharmaceutical manufacturing. job summary: Responsibilities:Execute manual and automated Fill/Finish operations, including equipment preparation, aseptic filling, product inspection, and packaging.
$17 - $18 an hourFull-timeExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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GMP, Contract Manufacturing, inspection, quality assurance, Aseptic Technician, Aseptic, Sterile, Sterile Injectables, Injectables, Document control, Compliance, Quality control, Filling, Aseptic technique, kitting.
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The Production Supervisor responsibilities are to coordinate the filling lines, assembly, and packaging activities to ensure proper timing, efficiency and quality for cGMP-regulated products.
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JOB DUTIESHas ownership for the daily formulation activities to ensure scheduled all scheduled tasks/events are completedIs responsible for critical steps in the formulation process including but not limited to, lab setup and process flows, in-process testing, API dissolution and final QS while ensuring safety, batch integrity and prevention or errors that could lead to product and or finical lossInitiate the production of batch documentation used for engineering and cGMP production.
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Under the supervision of a Senior Specialist or Associate Director, the Engineering EM&U Specialist is responsible for providing technical manufacturing support in the field of engineering, maintenance and utilities (EMU) and provides day-to-day engineering support for assigned area which may include vaccine bulk manufacturing, filling, lyophilization, packaging, and/or mechanical support utilities including power, HVAC, steam, WFI and controlled temperature units.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Production Associate – Fill (10:45pm – 6:45am) Every Friday and 2+ Week Nights Your role at Baxter: The Production Associate, Fill is an Hourly Non-Exempt position which contributes to our mission of saving and sustaining lives by inspecting, printing, filling, and sealing flexible containers which hold IV therapies, premixed drugs, renal therapies and other sterile solutions.
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Commissioning and qualification of liquid nitrogen supply systems, DI Water, autoclaves, isolators, filling and capping equipment, and airflow visualization studies. Skills; cGMP, commissioning, freezers, Validation.
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The External Manufacturing Specialist coordinates all aspects of contract manufacturing operations (filling, assembly, packaging) including day-to-day operations, ensuring timely completion of associated operations/documentation and assisting in the monitoring of cGMP compliance.
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Prior experience with biopharmaceutical, cell or gene therapy manufacturing across Upstream, Downstream and filling operations is a plus. Execute end to end unit operations for the manufacture of viral vector products in a cGMP environment using proper aseptic technique, good documentation practices, and sound scientific methods.
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filling cgmp jobs
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