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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