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Manufacturing Quality Engineer
•12 days ago
| Hours | Full-time, Part-time |
|---|---|
| Location | Manchester, Vermont |
About this job
Job Description
Job Description
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 & Rs, 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)
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 & Rs, 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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