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Quality Engineer AZ 60 - 75k (J#26739)

GENERAL RESPONSIBILITES
The Manufacturing Quality Engineer is responsible for the quality assurance of all products, quality system management, and manufacturing process quality and customer problem resolution. The MQE is also responsible for supporting continuous improvement activities.

SPECIFIC FUNCTIONS:
Program CMM for part measurement during part validation and ongoing quality control inspections.
Responsible for product design reviews and mold transfer process.
Resolution of internal Automotive/CI/Medical component quality problems.
Customer complaint cause and corrective action analysis.
Customer on-site quality resolution and/or quality reviews.
Specific production quality training for QA Auditors, IPIs and MQTs.
Audit of injection molding processes against the Master Process & Control Plans.
Development and maintenance of QAR (Quality Assurance Report) books.
Manage Tucson quality assurance operations during QA Managers absence.
Internal Audits, Customer Audits, and ISO/TS Audits.
Assist in procedure development and/or maintenance, quality validation after mold repair, including capability studies, gauge R&R, first article reports, etc.
ECN Approval for Automotive/Medical products.
MRB disposition of components.
Development and maintenance of the SPC database.
Member of Internal Auditing Team.
Develop measurement methods and design simple fixtures to enable accurate measurement of parts.
Operate various inspection instruments and hand held gauges
QUALIFICATIONS:
Engineering or Science degree desired, but will consider candidates work experience in the appropriate fields.
Minimum of 5 years quality engineering experience, with specific experience in medical devices/components desirable.
Strong measurement skills, including hands-on experience with calipers, micrometers, tool scopes, optical comparators and vision system.
Computer literate in programs such as Word, Excel, PowerPoint.
Strong analytical skills necessary.
Strong SPC knowledge and working experience.
Fluent in CMM programming, PCDMIS experience highly desirable.
Knowledge and experience in control plan development, product print and specification understanding, (understanding of Geometric Tolerancing).
Knowledge of molding process and procedures.
Fluent in ISO 13485 requirements
ASQ certified Quality Auditor and/or Quality Engineer highly desirable.
Ability to lift up to 50 lbs.
Ability to travel when needed.
Flexibility to work overtime and weekends.
Good safety record.
Other duties as may be required or requested.

Please e-mail your resume to parkwoodgroup@outlook.com in a WORD document.
 
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