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2 days
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$11.82/hr - $17.98/hr (Estimated)
<p>Apply</p> <p>Description</p> <p>CytoSorbents is seeking a Manufacturing/Production Associate to work 1st shift (6:00am - 2:30pm) in Princeton, NJ. The Manufacturing/Production Associate will perform GMP activities associated with producing, cleaning, and packaging of CytoSorb, a unique blood purification medical device used to control deadly inflammation in life-threatening illnesses in the ICU and cardiac surgery. Come join us in saving lives!</p> <p>Responsibilities</p> <ul> <li>Manufactures product according to company processes, procedures and GMP requirements </li><li>Controls equipment units or system that processes chemical substances into specified products </li><li>Observes chemical reactions; monitors gauges, signals, and recorders </li><li>Handles hazardous materials and hazardous waste in compliance with local, federal, and company guidelines </li><li>Receives notifications from the Shift Supervisor or designee to make specified operating adjustments </li><li>Practices appropriate clean room operations while assembling and handling the CytoSorb device </li><li>Records operating data such as process conditions, test results, and instrument readings </li><li>Draws samples of products for laboratory analysis </li><li>Performs activities associated with packaging products and materials for storage or shipment </li><li>Conducts packaging/shipping operations and inspects containers to verify conformance to specification </li><li>Inspects products prior to packaging/shipment and reports rejected products to the production department </li><li>Other duties as assigned </li></ul> <p>Requirements</p> <ul> <li>High School graduate with 3+ years of manufacturing experience in pharmaceutical or medical device cGMP compliant production/pilot plant or recent college graduate with 0 years of experience. </li><li>Good written and verbal language skills and ability to follow SOPS </li><li>Basic math skills </li><li>Ability to lift up to 50 pounds </li><li>Flexibility and attention to detail </li><li>cGMP and clean room experience is a plus </li></ul>
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