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Experience in Manufacturing and/or Electro-Mechanical Medical Device risk assessments. Coordinate activities through the Quality Engineering Manager and report regularly on the progress of activities.
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Evaluate proposed preclinical, clinical and manufacturing changes for regulatory filing strategies. Role: Regulatory Affairs Associate. Evaluate proposed preclinical, clinical and manufacturing changes for regulatory filing strategies.
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Participate with the Manufacturing Supervisor/Manager in setting and monitoring individual goals and cell performance metrics that continuously seek to improve the quality of operations. Be able to clearly communicate ideas, problems and solutions to all levels of manufacturing management in both written and oral form.
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Qualification: BE Any Engineering Please feel free to reach me at 732-355-7404 or email me at Required 5-7 years of experience as Manufacturing engineer from Aerospace/Medical device/Oil & Gas industry.
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Designing and improving equipment/processes, collaborating with vendors, preparing documentation, leading equipment design reviews and FAT, and driving continuous improvement using lean manufacturing tools.
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Must have knowledge on product design and med device manufacturing processes (swiss machine, injection moulding, assembly, extrusion, braiding, etc). - Must have some technical background to be able to interpret the technical nature of the component as well as any challenges they might be having during the process the process of manufacturing and delivering those time schedules.
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Familiarity with a variety of manufacturing processes (machining, injection molding, additive manufacturing, sheet metal, welding, etc.) This is Vydehi from Intellectt Inc. We currently have an opening for a Systems Engineer with one of our medical device clients.
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Works with Section Manager, Manufacturing Engineer and Team Lead. Works with Section Manager, Manufacturing Engineer and Team Lead. Assist with containment of Supplier Quality Non-Conformances. Analyze Scrap and Rework Data.
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Apply lean manufacturing tools to minimize waste and process variation, driving continuous improvement initiatives. Minimum of 1 year of manufacturing experience, preferably in Medical Device or Electronics industries.
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The manufacturing site is plastic injection mold. Bachelor’s degree is REQUIRED – NO EXCEPTIONS. (Preferred in Industrial or Manufacturing Engineering but will be open.) The manufacturing site is plastic injection mold.
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Plan, coordinate and control interdepartmental activity within quality assurance, manufacturing, procurement, engineering, production and logistic. Conducts daily, weekly, and/or monthly parts/material audit and physical cycle count and verifies alignment with SAP (parts number verification, batch number verification, proper part physical location.
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Provide assistance to subject matter experts (SME) for responsible product/project within the overall manufacturing and processing of pericardial tissue heart valve assembly, including leveraging of key knowledge of quality engineering principles.
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Develop material requirements from BOM's, monitor inventory levels, and coordinate the timely delivery of critically need hardware. Coordinate and expedite flow of materials meet production requirements.
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This is Vydehi from Intellectt Inc. We currently have an opening for a Manufacturing Engineer with one of our medical device clients. Minimum of 4-6 years of experience in the medical device and/or pharmaceutical manufacturing environment.
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Knowledge of and adherence to Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing. Knowledge of and adherence to Environmental Health and Safety and Quality guidelines as they relate to department clean room medical device manufacturing.
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manufacturing job Company: Intellectt Inc in Peoria, Arizona
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