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    Business Process Analyst - Fort Worth, United States - Rose International

    Rose International
    Rose International Fort Worth, United States

    3 weeks ago

    Default job background
    Upper Management / Consulting
    Description

    Date Posted: 05/17/2024

    Hiring Organization: Rose International

    Position Number: 464305

    Job Title: Business Process Analyst

    Job Location: Fort Worth, TX, USA, 76177

    Work Model: Onsite

    Employment Type: Temporary

    Estimated Duration (In months): 10

    Min Hourly Rate ($): 35.00

    Max Hourly Rate ($): 41.00

    Must Have Skills/Attributes: Business Analysis, FDA, Project Management



    Job Description



    **Only those lawfully authorized to work in the designated country associated with the position will be considered. **



    **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements. **



    Required Education and Experience:


    • At a Minimum: Bachelor's + 7 years relevant experience, MS + 4 years relevant experience, PhD + 3 years relevant experience



    Qualifications:


    • Project management expertise with proven results in multiple areas


    • Possess significant leadership skills to effect change


    • Has proven ability to develop/implement advanced processes, techniques related to product development and/or critical systems


    • Proven leadership track record of results


    • Capability to motivate complex teams cross-functionally; directs strategic and business goals


    • Expert knowledge of ISO, FDA, MDD and regulations applicable to the design and development of medical device/science/technology


    • Provides expert input to develop solutions to complex problems that require the regular use of creativity, and originality


    • Robust process management, problem solving skills and superior presentation capabilities



    Business Process Analyst Responsibilities:


    • Author Risk Management documentation for Class II & III Medical devices in compliance with ISO 14971 & EUMDR


    • Lead the development of Design History Files for class II & III Medical Devices in compliance with ISO 13485, EUMDR, MDSAP, and other standards/regulations relevant to medical Device Design & Development


    • Author Critical Design History File Documents, and lead cross-functional discussions to ensure alignment through the entire Design & Development Team


    • Serve as the representative for Design Control Team at cross-functional core team meetings


    • Lead design reviews, assign and review action items or delegate these tasks


    • Works with wide latitude for unreviewed action or decision and represents the corporate direction in science and technology. Key functional expert who manages, direct and coordinates the activities of a specific area


    • Strategic and/or management interface


    • Supports engineering or scientific decision making by providing advice and recommendations to global project teams


    • Develop concepts and propose approach, to address identified ophthalmic medical device/science/technology needs


    • Originate and apply complex concepts and propose new and unique approaches, methods, procedures and designs with regular use of creativity and originality to research and/or development



    Benefits:

    For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.



    California Pay Equity:

    For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.

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