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Nolato GW Tucson Manufacturing Quality Engineer

Nolato GW Tucson is looking for a Manufacturing Quality Engineer who will be 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.

Nolato GW is a part of the Nolato group. Nolato is a Swedish publicly listed group with operations in Europe, Asia and North America. We develop and manufacture products in polymer materials such as plastic, silicone and TPE. Nolato GW Plastics is a global leader in precision injection molding and contract manufacturing to the world’s most successful companies. Join an organization that is respected throughout the industry for its advanced technology, quality, and innovation – all the while enjoying the benefits of stable ownership, a collaborative culture, professional development, continuing education, global opportunities, and an exceptional benefits package.


 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, IPI’s and MQT’s.
 Audit of injection molding processes against the Master Process & Control
 Development and maintenance of QAR (Quality Assurance Report) books.
 Manage Tucson quality assurance operations during QA Manager’s 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.
 Awareness and compliance to ISO 14000 requirements per company policies
and procedures.
 Operate various inspection instruments and hand held gauges

 Engineering or Science degree desired, but will consider candidate’s 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, CMM experience highly desirable.
 Knowledge and experience in control plan development, product print and specification understanding, (understanding of Geometric Tolerancing).
 Customer interface experience.
 Knowledge of molding process and procedures.
 Experience in molded product quality control desired.
 FDA/ISO/TS quality system knowledge and experience necessary (any or all).
 ASQ certified Quality Auditor and/or Quality Engineer highly desirable.
 Good communication skills.
 Ability to lift up to 50 lbs.
 Ability to travel when needed.
 Other duties as may be required or requested.


Tucson, USA

Apply by

September 23, 2022

Contact person

Cathy Tempesta [email protected]