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    Quality Engineer - Ocean Grove, United States - Medline Gruppe

    Medline Gruppe
    Medline Gruppe Ocean Grove, United States

    3 days ago

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    Description
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    Job Description - Quality Engineer | Neptune, NJ (QUA0101SY)
    Job Description
    Quality Engineer | Neptune, NJ

    (

    Job Number:

    QUA0101SY

    )
    Primary Location

    :

    US-NJ-Neptune
    Description

    JOB SUMMARY:
    Medline has an immediate opening for a Associate Quality Engineer supporting our manufacturing site in Neptune, NJ.

    This role us under broad supervision, responsible for independently setting basic quality standards for both in-process while leading efforts to develop methods for testing, sampling and training.

    Evaluate production process, recommend improvements, qualify and conduct vendor management, generate and maintain DMR's, product specifications, design control files, and CE technical files.


    MAJOR RESPONSIBILITIES:


    Manage the development and implementation of methods and procedures for process control, process validation, process improvement, testing, and inspection to ensure that products are ideal and functional.

    Design experiments to understand sources of variation affecting products and processes. Applies statistical process control (SPC) methods for analyzing data to evaluate the current process and process changes.
    Design and perform experimental product testing and analysis to maintain quality levels and minimize defects and failure rates. Generate and analyze reports and defective products to determine trends and lead corrective actions. Use concepts of probability and statistical quality control to guide decisions.

    Direct and collaborate with supplier representatives on quality problems, ensure corrective action implementation (CAPA, SCAR), and contribute to supplier quality improvement programs.

    Lead supplier qualifications.
    Provide Quality expertise in Product Development, Design Control activities, Risk Management, and CE Technical Files.
    Responsible for building appropriate product documentation (e.g. Device Master Records) in compliance with applicable regulations. Work with Regulatory Groups and Suppliers to produce 510K submissions, letters to file, etc., as required.
    Coordinate product testing with internal and external laboratories as required.
    Ensure compliance with domestic and international regulations associated with product lines and processes. Perform quality reviews of design documentation for compliance with stated requirements, including vendor quality documents and company quality records.
    Lead investigations of product and process non-conformances and out-of-specification results and develop effective corrective and preventive actions (CAPA).
    Qualifications

    Education
    Typically requires a Bachelor's degree in Engineering, Science, Math or other related technical field.
    Work Experience
    At least 2 years of experience in the Quality or Engineering.
    Knowledge / Skills / Abilities

    Experience developing ways of accomplishing goals with little or no supervision, depending on oneself to complete objectives, and determining when escalation of issues is necessary.

    Experience using time management skills to prioritize, organize, and track details in order to meet deadlines of multiple projects.
    Experience problem solving, overcoming obstacles, and reaching a positive and successful solution through mathematical or systematic operations.
    Experience using MS Office Suite products (Word, Excel, PowerPoint, Outlook ).
    Intermediate Skill Level in Microsoft Excel (for example:

    conditional formatting, tables, formulas, charting)
    Working knowledge of government and industry quality assurance codes and standards (e.g. 21 CFR 820, ISO13485).
    Position requires up to 15% travel.


    PREFERRED JOB REQUIREMENTS
    At least 2 years of industry experience in Medical Devices, Drugs, and/or fields directly related to the role.
    Medline Industries, LP is an equal opportunity employer.

    Medline evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status or any other legally protected characteristic.

    Medline is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to and let us know the nature of your request along with your contact

    VETERANS AT MEDLINE
    Medline recognizes the experience and dedication veterans bring to the workplace. We take pride in the career paths provided to our employees.

    Our military employees add tremendous leadership skills and a broad range of talents which help us drive the healthcare solutions needed for today and tomorrow.

    #J-18808-Ljbffr

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