C. R. Bard, Inc.

  • Quality Engineer I

    Posted Date 6 days ago(10/9/2018 11:45 AM)
    Job ID
    Career Level
  • Overview

    Bard has joined BD, together advancing the world of health.  BD Urology & Critical Care, formerly Bard Medical, is looking to fill the position of Quality Engineer I located in Covington, GA.

    Summary of Position with General Responsibilities

    This position performs various quality-engineering functions and associated support tasks in developing knowledge and experience in the areas of Quality Assurance/Document Control/Design Control.  This includes working to support Design Control projects as well as other duties in support of the Quality System, Design Control System, Document Control, Manufacturing, and the R&D/Product Development departments.

    Essential Job Functions


    • Represents the Corporation, Division and Quality Department in a professional manner
    • Participates on Project Team as Quality Representative. Ensures that principals of Design Control are applied to Product and Process Changes and New Product Development
    • Creates and reviews Quality System Documents
    • Creates and reviews Product Documents
    • Creates and reviews Test Methods and addresses Test Method Validation
    • Creates/reviews Protocols, Process and Product Validations, Stability Protocols
    • Provides guidance to test technicians/quality inspectors as required
    • Creates and reviews documents required for Design History File
    • Creates and reviews Risk Assessments such as FMEA, FMECA or FTA
    • Performs Internal or Supplier Quality System Audits
    • Ensures compliance to Department and Division procedures
    • Participates and has membership in trade and/or professional organizations to ensure that state-of-the-art industry standards are communicated into the division in an efficient, timely, and accurate manner
    • Interfaces with manufacturing facility or other Division Facilities
    • Supports root cause investigations and other steps of the CAPA process
    • Travels as required by the above duties and responsibilities

    Basic Qualifications


    To perform this job successful, an individual must be able to perform each essential duty satisfactorily.  The requirements listed in this section and below are representative of the knowledge, skill and/or ability required.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. 

    • Ability to perform detailed engineering work under direction of a Senior Engineer or Quality Management. May require consultation and direction to complete the essential duties and responsibilities
    • Understands basic applied statistics
    • Ability to participate on teams and maintain positive work environment with those teams.
    • Good communication skills (verbal, written, and presentation)
    • Understands Basic Fundamentals of Engineering Principles
    • Ability to effectively manage time
    • Ability to handle multiple task assignments
    • Ability to translate quality requirements into product specifications
    • Ability to interpret Regulations, Corporate, Division and Department Procedures


    Education and/or Experience

    • BS in Engineering, Engineering Technology, Science a minimum
    • American Society of Quality (ASQ) certification (CQE, CQA, CQM, etc.) preferred
    • Minimum 1 years of experience with FDA regulated industry

    Physical Demands

    Employee may be required to sit, bend, stoop, use keyboard, see, talk and hear.  May occasionally lift objects of 10 to 25 lbs.  Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

    Work Environment

    • Office and manufacturing environments
    • May include visits to clinical sites or hospitals
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