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    Senior Design Quality Engineer - Andover, United States - TransMedics Group, Inc.

    TransMedics Group, Inc.
    TransMedics Group, Inc. Andover, United States

    1 week ago

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    Description

    JOB DESCRIPTION

    Position:
    Sr. Design Quality Engineer

    Reports to:
    Senior Director, Quality Assurance

    ESSENTIAL JOB RESPONSIBILITIES AND DUTIES INCLUDE:

    • Responsible for the overall health of design control process. Responsible for assuring NPI and sustaining projects meet customer expectations, and regulatory requirements.
    • Partner with Development and Engineering departments and ensure that design control requirements are being met in an effective manner in order to achieve quality by design, including those for design verification, validation, specification and procedure development, risk management, and design review
    • Provides input to design and manufacturing engineering project DHF deliverables including material specifications, drawings, inspection procedures, and manufacturing procedures, to ensure that the resulting products can be adequately manufactured and tested. Review DHF files for accuracy and completeness and provide guidance on FDA compliance and procedures.
    • Review and approve design control related Change Notices (CNs) within the documentation system as applicable.
    • Create processes and process improvements to ensure consistent implementation of internal requirements and external regulations and standards.
    • Represent the design quality functions for the review and approval of designated design outputs.
    • Act as a subject matter expert on design control process and Quality Engineering. The Quality Engineering subjects are Risk Management, Test Method Validation (TMV), Statistics, Reliability Engineering, Process Validation (PV).
    • Support the quality management system as required.
    • Perform other TransMedics task and duties as required.

    REQUIREMENTS:

    • BS in Engineering with 8 years of related experience or equivalent combination of education and experience.
    • Medical device development control experience required.
    • Working knowledge of Software development lifecycle desired.
    • Working knowledge and practical application of 21 CFR Part 820, ISO 13485, ISO 14971.
    • Practical knowledge and experience using Minitab or other statistical analysis tools.
    • Understanding and application of Gage R&R and Measurement System Analysis desired
    • Process validation experience including IQ/OQ/PQ desired.
    • Ability to communicate ideas and information clearly, effectively and concisely.
    • Highly detail oriented with strong organization and prioritization skills.

    EDUCATION:

    • BS in Engineering or other technical discipline
    Notice of Recruitment Fraud

    It has come to our attention that individuals who are unaffiliated with TransMedics are posing as representatives and engaging with candidates regarding fake job opportunities.

    These fraudsters may request payment and/or financial information from you. These opportunities are not authorized by TransMedics.

    Please note that our recruiting process does not include asking candidates for payments of any kind and/or financial information under any circumstances.

    For individuals in the United States, the following link may be useful in protecting yourself: Please note that TransMedics is not responsible for the content of this website.

    For individuals outside of the United States, please check with your local authorities.

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