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  • Quality Manufacturing Engineer

    Cook Medical (Spencer, IN)



    Apply Now

    Overview

     

    The Quality Engineer serves as the lead quality representative of certain product lines within product development, manufacturing, post-market surveillance, and/or CAPA.

    Responsibilities

    - Perform work per external and internal quality standards.- Interface with internal and external groups on quality-related issues.- Support product development and transfer to manufacturing.- Facilitate development and implementation of production controls. (e.g. qualification, process capability, sampling plans, validation, etc.)- Perform investigation of product non-conformance/complaints, root cause analysis, monitoring/trending of process and product, and escalation of identified issues.- Plan, review, and approve change requests.- Execute risk assessment as needed and facilitate development and completion of risk file documentation.- Conduct Risk-based decision making and effective resolution of issues.- Lead or support CAPAs as necessary.- May interface with internal or 3rd party audits. (e.g. FDA, Notified Body, etc.)- Drive continuous improvement efforts through facilitating, leading, and collaborating with cross function teams including quality, engineering, production, clinical, and regulatory affairs.- Provide leadership in the understanding of medical device regulations and best practices.- Manage conflict resolution as it relates to technical situations.- Must maintain all training requirements for the position, while seeking out opportunities for continuous development and growth.- Adhere to the Quality Management System and its processes to meet FDA 21 CFR 820, ISO 13485, and other applicable regulatory requirements.

    Qualifications

    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.

     

    - Bachelors Degree in Engineering or a Technical Life Science Degree.- Demonstrates knowledge of medical device regulation (ISO 13485, 21CFR) and risk management (ISO 14971)- Professional certification (e.g. ASQ, Six Sigma, etc.) preferred.- Proficiency in statistical, quality and continuous improvement methods and tools.- Proficiency in the Microsoft Office suite of products (Word, Excel, PowerPoint, and Outlook) is required.- Strong organizational skills.- Critical thinking and attention to detail required.- Excellent verbal communication skills and technical writing.

     

    Requisition ID2025-16669

     

    Posting Date1 week ago(7/24/2025 8:55 AM)

     

    Job Location(s)Spencer IN United States

     

    Job LocationsUS-IN-Spencer

     

    TravelLess than 10%

     

    Position TypeFull Time

     

    CompanyCook Inc - Spencer

     

    CategoryQuality

     


    Apply Now



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