<ul> <li>Investigation of product complaints </li><li>Troubleshooting manufacturing processes </li><li>Product inspection / testing, data collection and basic analysis </li><li>Review device history records for accuracy and lot traceability </li><li>Review of documentation for correctness & accuracy </li><li>Assist ongoing product development and manufacturing </li><li>Provide support to quality instrumentation and calibration system </li><li>Assist in generating required documentation for Product Development deliverables. </li><li>Assist in writing technical report. </li><li>Data entry </li></ul> <p>Qualificationsarrow_right</p> <ul> <li>Quality experience, preferable in medical device or similar industry that has similar requirements for lot history control (regulated industry). </li><li>MS Word/Excel </li><li>Blueprint reading </li><li>Good math skills </li><li>Instrumentation and calibration experience </li><li>Willingness and eager to learn </li></ul> <p>The Freudenberg Group is an equal opportunity employer that is committed to diversity and inclusion. Employment opportunities are available to all applicants and associates without regard to race, color, religion, creed, gender (including pregnancy, childbirth, breastfeeding, or related medical conditions), gender identity or expression, national origin, ancestry, age, mental or physical disability, genetic information, marital status, familial status, sexual orientation, protected military or veteran status, or any other characteristic protected by applicable law.</p>