Cytosorbents Medical Inc
Process Operator/Production Associate - 1st Shift
Cytosorbents Medical Inc, Princeton, New Jersey, United States, 08540
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!
Responsibilities
Manufactures product according to company processes, procedures and GMP requirements Controls equipment units or system that processes chemical substances into specified products Observes chemical reactions; monitors gauges, signals, and recorders Handles hazardous materials and hazardous waste in compliance with local, federal, and company guidelines Receives notifications from the Shift Supervisor or designee to make specified operating adjustments Practices appropriate clean room operations while assembling and handling the CytoSorb device Records operating data such as process conditions, test results, and instrument readings Draws samples of products for laboratory analysis Performs activities associated with packaging products and materials for storage or shipment Conducts packaging/shipping operations and inspects containers to verify conformance to specification Inspects products prior to packaging/shipment and reports rejected products to the production department Other duties as assigned
Requirements
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. Good written and verbal language skills and ability to follow SOPS Basic math skills Ability to lift up to 50 pounds Flexibility and attention to detail cGMP and clean room experience is a plus
Responsibilities
Manufactures product according to company processes, procedures and GMP requirements Controls equipment units or system that processes chemical substances into specified products Observes chemical reactions; monitors gauges, signals, and recorders Handles hazardous materials and hazardous waste in compliance with local, federal, and company guidelines Receives notifications from the Shift Supervisor or designee to make specified operating adjustments Practices appropriate clean room operations while assembling and handling the CytoSorb device Records operating data such as process conditions, test results, and instrument readings Draws samples of products for laboratory analysis Performs activities associated with packaging products and materials for storage or shipment Conducts packaging/shipping operations and inspects containers to verify conformance to specification Inspects products prior to packaging/shipment and reports rejected products to the production department Other duties as assigned
Requirements
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. Good written and verbal language skills and ability to follow SOPS Basic math skills Ability to lift up to 50 pounds Flexibility and attention to detail cGMP and clean room experience is a plus