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OPEN POSITION

Manufacturing Quality Engineer

Join Nolato GW at our Bethel, Vermont plant! We are looking for a Manufacturing Quality Engineer,  who will be responsible for ensuring the quality of all products, quality system documentation, manufacturing process quality and customer problem resolution.

Nolato GW is a global leader in precision injection molding and contract manufacturing for the world’s most successful healthcare, automotive, and industrial OEMs.

Join an organization that is respected throughout the industry for our advanced technology, quality, and innovation – all while enjoying the benefits of stable ownership, a collaborative culture, professional development, continuing education, global opportunities, and an exceptional benefits package.


JOB TITLE:

Manufacturing QualityEngineer

 

DEPARTMENT:

Bethel Operations

REPORTS TO:

Quality Assurance/Continuous Improvement Manager

 

DESCRIPTION:

The Manufacturing Quality Engineer is responsible for ensuring the quality of all products, quality system documentation, manufacturing process quality and customer problem resolution.

 

SPECIFIC RESPONSIBILITIES:

  • Participates in product design reviews and Engineering hand-off approval.
  • Resolves internal product quality problems to reduce defects/scrap.
  • Champions product customer complaint cause and submits corrective action plans in the 8D or customer format.
  • Participates in and assists in resolving customer on-site quality issues and/or quality reviews.
  • Oversees and supports Quality Technicians.
  • Performs specific quality training for Quality Technicians, IPI’s, and MQT’s.
  • Develops and maintains QAR’s (part specific work instructions).
  • Performs daily 5S and process audits of select injection molding machines against the Master Process and Control Plans.
  • Verifies and validates reports after mold repair, including capability studies, gauge R & R’s, first article reports, etc.
  • Annually revalidates medical/automotive components per customer requirements.
  • Develops and maintains SPC database for medical components.
  • Performs daily inspection of product/process 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.
  • Minimum of 5 years quality engineering experience, with specific experience in medical devices/components desirable.
  • Knowledge/experience with measurement equipment.
  • Computer literate in programs such as Word, Excel, and PowerPoint.
  • Solid statistical knowledge and practical experience.
  • Knowledge and experience in control plan development, product print and specification understanding, and customer interface experience.
  • Knowledge of molding process and procedures desired.

Location

Bethel, Vermont, USA

Apply by

March 01, 2024

Contact person

Cathy Tempesta [email protected]