Engineer 1, Manufacturing

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    "datePosted": "2026-04-13T04:00:00.000Z",
    "description": "<h2>Overview</h2>\n<p>The Manufacturing Engineer plans, directs, and coordinates manufacturing processes for medical device products, and supports Operations in a way to assure a quality product is produced in a timely manner. The Production Engineer works with Operations, Quality Assurance and Regulatory Affairs to improve existing product designs and processes to increase throughput, decrease operational costs, or improve quality.</p>\n<h2>Responsibilities</h2>\n<p>- Work with Operations Managers and outside Vendors to create methods/machines to help with capacity of products.- Work with Product Development Engineers to develop processes for new products.- Work with Operations, Accounting, and Global Product Managers to increase profit margins of current products which do not meet company requirements.- Train all relevant personnel on new processes.- Document cost savings.- Write and execute validation protocols.- Assure projects follow design controls established by QSPs (Quality System Procedures).- Provide support to the calibration department in writing/performing calibration procedures.- Work with Quality Assurance and Product Development to verify/validate critical processes or products.- Work with management to establish project timeliness,and project justification.- Act as resource for operational departments for materials, equipment and process upgrades.- Must maintain all training requirements for the position, while seeking out opportunities for continuous development and growth.- Prepare and maintain accurate documentation consistent with the requirements of pertinent regulations and Cook’s Quality Management System where applicable.</p>\n<h2>Qualifications</h2>\n<p>- Bachelor’s Degree in Engineering (Biomedical, Mechanical, Production, or Manufacturing Engineering preferred)</p>\n<p>- Preferred knowledge of process validation, design for manufacturing, statistics and lean manufacturing principles</p>\n<p>- Preferred knowledge of medical device quality standards ISO13485/FDA practices,GMP and similar regulated industry standards.</p>\n<p>- Preferred knowledge of 3D Modeling software (Creo, Solid Works, etc)</p>\n<p> </p>\n<p><strong>Physical Requirements:</strong></p>\n<p>- Works under general office environmental conditions.- Sitting for extended periods, utilizes close visual acuity for working with computers, equipment, etc.- Frequently required to sit, stand, walk, and communicate</p>\n<p> </p>\n<p><strong>**Qualified candidates must be legally authorized to be employed in the United States.  Cook does not intend to provide sponsorship for employment visa status (e.g., H-1B or TN status) of this employment position.**</strong></p>",
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