C. R. Bard, Inc.

  • Supplier Quality Engineer

    Posted Date 3 weeks ago(7/27/2018 5:02 PM)
    Job ID
    2018-11949
    Career Level
    experienced
    Division
    BOC Reynosa
    Relocation
    no
    Location
    MX-Reynosa, Tamaulipas
  • Overview

    Supplier Quality Engineer

    • Maintain Supplier Management Program.
    • Develop the Supplier audit schedule and ensure supplier audits are completed as scheduled.
    • Timely follow-up on supplier quality issues.
    • Maintain control of quality costs for the supplier management program including incoming sampling and personnel costs.
    • Ensure full compliance with policies, procedures, QSR and ISO.
    • Solve the manufacturing and Quality problems to support de manufacturing operation related with the supplier issues and responsible for follow up of the Quality improvements with them.

    REQUIREMENTS:

    ü Bachelor Degree in Engineering. Master degree desired or equivalent in experience.

    üMinimum 6 years in the related area.

    ü Excellent oral and written communication skills

    in English

    üKnowledge in any of the following areas (preferred):

    ISO 13485: 2003 “Medical Devices” Quality Management Systems Requirements for Regulatory Purpose”. 

    Additional Desirable Qualifications Skills and Knowledge

    Supplier Quality Engineer

    • Maintain Supplier Management Program.
    • Develop the Supplier audit schedule and ensure supplier audits are completed as scheduled.
    • Timely follow-up on supplier quality issues.
    • Maintain control of quality costs for the supplier management program including incoming sampling and personnel costs.
    • Ensure full compliance with policies, procedures, QSR and ISO.
    • Solve the manufacturing and Quality problems to support de manufacturing operation related with the supplier issues and responsible for follow up of the Quality improvements with them.

    REQUIREMENTS:

    ü Bachelor Degree in Engineering. Master degree desired or equivalent in experience.

    üMinimum 6 years in the related area.

    ü Excellent oral and written communication skills

    in English

    üKnowledge in any of the following areas (preferred):

    ISO 13485: 2003 “Medical Devices” Quality Management Systems Requirements for Regulatory Purpose”. 

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