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Conduct all job activities in accordance with cGMP and EHS requirements. Knowledge of products and technologies including but not limited to: Emerson DeltaV, Rockwell Allen Bradley. Support the hardware operation of all GMP/ Non GMP manufacturing systems (Process Automation Systems and Building Automation Systems) in the Manufacturing facilities at Syracuse, NY.
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Ensure that packaging’s complies with hazardous materials transportation, FDA, EPA, cGMP, and ISO regulations and guidelines. Ensure compliance with applicable requirements for domestic and international multi-modal safe transport of listed hazardous materials products including the United States Department of Transportation (DOT), International Air Transport Association (IATA), International Maritime Dangerous Goods (IMDG), and United Nations (UN.
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Coordinate with external contractors to facilitate instrument maintenance and repairsAuthor Standard Operating Procedures for new instruments/softwareWhile working in a cGMP environment, he/she must maintain operational compliance with U.S. and international regulatory agencies (i.e. FDA, NRC, Health Canada, OSHA, etc.
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Maintain compliance with SOP, current Good Manufacturing Procedures (cGMP) and regulatory guidelines. With donation centers and team members throughout the U.S., Octapharma Plasma, Inc. collects plasma to create life-saving medicines for patients worldwide.
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Maintain all work areas in a well-organized, clean and tidy manner at all times in compliance with cGMP requirements. Engage in cage movement, maintain product segregation, retrieve and organize raw materials, and ability to learn fork truck operation.
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Certified in operation of at least one high speed manufacturing equipment efficiently and effectively, in some cases highly automated, using HMI/SCADA interfaces. Must be able to push a wheeled cage that can weigh up to 600 lbs fully loaded.
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Hairnet, clean room gowns and/or lab coats are required. 1-2 years' experience in FDA regulated manufacturing environment and GMP is desired. Normal working hours for this position are 2nd Shift Monday - Friday from 2:00pm - 10:30pm.
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Working knowledge of cGMP facility construction, remodelling, electrical, HVAC, compressed air mechanical and plumbing for facilities. Virbac Animal Health is seeking a Construction and Facilities Manager for our Maintenance Team. The Construction & Facilities Manager is responsible for managing the construction activities, ensuring building maintenance and supporting utilities maintenance.
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Work with the department Associate Team Leaders and Team Leaders to ensure compliance with all cGMP, ISO and FDA guidelines for warehouse activities. Experience with the safe and efficient use material handling equipment such as a floor jack, hand truck, order picker, and forklift is preferred.
$17.5 an hourFull-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Follow Current Good Manufacturing Processes (cGMP). On the job training & great hourly pay + 401K with Company Match, Profit Sharing, Health Insurance, Employee Assistance Program, Life Insurance, Paid Time Off, Direct Payroll Deposit, Tuition Reimbursement, 30% Employee Discount, Employee Referral Bonuses.
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The QC Analytical Scientist’s primary responsibility is to perform routine to complex QC testing pertaining ELISA testing and Cell Based Assays in accordance with cGMP regulations. Extensive knowledge of GMP regulations in a cGMP manufacturing environment.
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Service HPLCs and similar analytical instrumentation utilized in pharmaceutical ingredient and finished product testing and release produced under cGMP conditions. CONSIDERED EXPERIENCE INCLUDES: Metrologist Maintenance Calibration Technician Metrology Analytical Laboratory Instrumentation Validation Chromatography Mass Spectrometry HPLC UPLC GC MS GC/MS Chemistry Analyzers #DiedreMoire #JobSearch #JobHunt #JobOpening #Hiring #Job #Jobs #Careers #Employment #fieldservicejobs #technicianjobs #LabTechnicianJobs #MetrologistJobs #CalibrationTech.
ExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Inspection, Quality inspection, Visual inspection, cgmp, Production, Assembly, gmp, fda compliance. Inspection,Quality inspection,Visual inspection,cgmp. They will also inspect finished products while following cGMP guidelines and company packaging standards.
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General quality / quality control / production experience in a cGMP facility required. 1 or more years of relevant quality / quality control / production experience in a cGMP facility required.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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The Training and Development Coordinator shall be held accountable for the enforcement of compliance requirements, including cGMP, housekeeping and documentation. The Training and Development Coordinator is expected to fully comply and enforce all cGMP guidelines, as well as with the standards and policies of Legacy Pharma Solutions.
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cgmp job in Hazelwood, MO
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