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Hyster-Yale Group, Inc. (HYG), a world-class manufacturer of industrial lift trucks, has an outstanding opportunity for an exceptional and talented Vehicle Validation Engineer based at our Greenville, NC Manufacturing Site.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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The Packaging Engineer will be managing the design, planning, validation, and implementation of new packaging technologies. DSJ Global is currently partnered with a leading Consumer Hygiene Products Producer who is looking to add a Packaging Engineer to their growing team.
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Perform system integration and validation testing to ensure compliance with specifications. Job Title: Automation Engineer. Strong programming skills in PLCs (Allen-Bradley, Siemens) and HMIs (Wonderware, FactoryTalk.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Knowledge of pharmaceutical manufacturing processes, validation, and investigational requirements. + Provide QA review and approval of validation protocols and reports for manufacturing process, cleaning process, equipment and facility validation activities, for new and existing procedures, change controls, deviations and investigations.
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Prepares, reviews and approves production, validation, audit reports and/or master batch record documents, procedures, and rationales. Establishes and supervises quality programs and plans (e.g. validation, QAT, supplier certification.
Full-timeExpandApply NowActive JobUpdated 23 days ago - UpvoteDownvoteShare Job
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Provide documentation to ensure the consistent manufacture of new products; including batch records, production instructions, validation and stability protocols in the development and commercialization of the products.
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The PositionThe Validation Engineer III, Equipment & CSV will provide direct validation support to pharmaceutical development and manufacturing operations. Under little to no supervision the Validation Engineer III, Equipment & CSV will perform quality functions to ensure accurate execution and documentation of all activities and projects as assigned.
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The Validation Engineer III, Equipment & CSV will provide direct validation support to pharmaceutical development and manufacturing operations. Validation Engineer III, Equipment & CSV.
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Assist in the implementation for improved site validation activities and the quality systems related to these activities. Author/Review process validation protocols and validation summary reports.
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This position is a Quality IT Systems Manager/Computer Systems Engineer that possesses knowledge of pharmaceutical manufacturing software platforms, focused primarily on the Salesforce platform and other hosted systems.
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Packaging Engineer | Greenville, NC Direct Hire-Full Benefits | Relocation Provided Job Summary: Manage the design, planning, validation and implementation of new packaging technologies, materials, line extensions, package/product improvement and technical service for Health Partners that meet product offering requirements.
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As a key contributor to OMRON America’s manufacturing operations, the Sr. Manufacturing Test Engineer is responsible for the development, validation, implementation, and maintenance of the manufacturing control, test and automation systems used in the manufacturing of our highly complex electromechanical products and their embedded systems.
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Participate as the validation representative in project team activities and process design to insure CGMP compliance and interdepartmental consistency within the validation program. Broad based knowledge of regulatory compliance requirements related to validation and relevant production controls.
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BS Chemical Engineering degree with 6+ years in combination of project/ process engineering, product/process development, and regulatory requirements in polymers, minerals, chemical, and/or food science industries.
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