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Check and document weight of all powder blends when received from Blending Department Copress/Encapsulate product as specified in the batch Manufacturing Records. Job Summary The Manufacturing Operator reports to the Shift Supervisor and is responsible for learning and performing various pharmaceutical manufacturing techniques including dispensing, blending and granulation, compression, encapsulation, and coating.
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The QA/QC Field Engineer will champion the quality control efforts on site, including document review during preconstruction and construction. The QA/QC Field Engineer will champion the quality control efforts on-site, including document review during preconstruction and construction.
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Select required cutting tools, tool grades, and proper speeds and feeds from programming document. Clark-Reliance is a world class manufacturing company, serving customers in over 120 countries in the power generation, refining, gas processing, and chemical industries.
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The full-time, multi-disciplinary position will have the opportunity to potentially work in a wide variety of sectors including agriculture and forestry (AFOLU), CFCs/HCFCs, chemical, coal mine methane, livestock (dairy and hog farms), manufacturing, oil & gas, renewable energy, transportation and waste.
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Read and interpret process sheets, gage, Deburr and clean parts, make minor offset changes (if required), change set ups and document information on check sheets, keep dimensional data on run charts, frequently utilize measuring devices and assess product acceptance based on blueprint specification(s), run all equipment in the entire work loop and produce product per standard work.
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Requires Experience in manufacturing software (ERP, MRP, MPS, WMS) Streamline the document management flow (BOL's, scan folders, archives, etc.) Document processes and continuously improve Distribution Center Processes.
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The Quality Assurance Document Control Specialist role is an exempt position responsible for supporting the document management process within a cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment.
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Tube Supply clients are leading oil and gas service companies, OEMs, and manufacturing centers spanning as far as Canada and Mexico in addition to the United States. High level computer and document processing skills.
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Develop, optimize, and document manufacturing processes for carbon fiber composite rifle stocks, ensuring adherence to quality standards, safety regulations, and production goals. The Composite Process Engineer will play a vital role in the development and improvement of the manufacturing process for carbon fiber composite rifle stocks.
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Order materials, verify materials and production specifications, perform quality checks, monitor and respond to KPI data prompts, set up machine for various product styles, and classify finished product through direct interaction with advanced Manufacturing Execution System and Document Management System, and other computer applications as appropriate.
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Minimum of 12+ years of experience in implementing Siemens PLM and Mfg solutions with extensive Teamcenter Product Knowledge in the areas of CAD Mgmt, Item & BOM Mgmt, Document Mgmt, Change Mgmt, and ERP integrations.
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Design, document and implement methods and procedures for inspection and test Improving plant quality performance, and customer satisfaction through process improvement techniques such as SPC, FMEA, DOE, Lean manufacturing etc.
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Experience implementing Lean Manufacturing and Six Sigma methodologies including statistical analysis techniques (Design of Experiments, Statistical Process Control (SPC), etc) preferred. Sanmina Corporation (Nasdaq: SANM) is a leading integrated manufacturing solutions provider serving the fastest-growing segments of the global Electronics Manufacturing Services (EMS) market.
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Conduct and appropriately document aseptic production of radiopharmaceutical drug product and radioisotopes via strict adherence to manufacturing batch records and affiliated SOPs. Aseptic production of radiopharmaceutical drug product and radioisotopes in accordance with established manufacturing batch records.
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This position supports the development of Operational Excellence by increasing team members’ awareness of the manufacturing plant’s continuous improvement program and by leading core management systems programs including corrective action, internal audit, and document control.
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