The Manufacturing Quality Engineer (MQE) is responsible for ensuring the quality of all products. They will also be required to review/maintain our client's quality system documents and records. The MQE will also be involved in new mold/product validation, cross qualifications, and continuous improvement activities. The MQE will be assigned daily 5S and/or process audits.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
·       Participate in product design reviews
·       Resolve internal product quality issues to reduce defects/scrap
·       Participate on the Correction and Preventative Action (CAPA) team
·      Participate or assist in resolving customer on-site quality issues and/or quality reviews
·      Support      Quality      Assurance       Technicians        by     improving      gauging methods/efficiencies
·       Perform part specific quality training for Quality Assurance Technicians
·       Performs daily 5S and process audits as assigned
·      Verify and validate reports after mold repair, including capability studies, gauge R & R’s, first article reports, etc.
·       Develop and maintain statistical process control (SPC) database for new medical components
·       Performs daily inspection of product on the production floor
·       Supports Internal Audits, Customer Audits, and ISO/QS Audits
·       Assists in procedure development and/or maintenance
·      Responsible for MRB disposition of nonconforming products in the absence of the Quality Manager
·       Other duties as assigned
QUALIFICATIONS:
·       Engineering or Science degree desired
·       Knowledge/experience with measurement equipment (CMM desired)
·      Computer literate in programs such as Word, Excel, and PowerPoint and Minitab
·       Solid statistical knowledge and practical experience
·       Knowledge of injection molding process desired
·       ISO system knowledge and experience desired
·       Good communication skills
·       Ability to lift up to 50 pounds
·       Ability to travel when needed (less than 5% of the time)
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