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Quality Engineer

Welch Fluorocarbon, Inc.

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Dover, NH
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Job Description

As posted by the hiring company

Job Overview:

Description

  

Welch Fluorocarbon, Inc., a UFP Technologies Company is currently looking to fill the role of Quality Engineer. Since 1985, Welch Fluorocarbon has specialized in providing thermoformed and heat-sealed products to a variety of customers utilizing the best, thin, high-performance films. Our corporate culture is a true team environment where there is a presence of clear purpose, the strength of real community and the celebration of individual creativity. The foundation of our culture is based on the core ideology of balance.  


Essential Responsibilities:

  • Responsible for managing the quality aspects of materials and services provided by external suppliers.
  • Conducting supplier audits, and collaborating with suppliers to address quality issues.
  • Conduct root cause analysis and implement solutions for defective materials.
  • Ensure suppliers adhere to regulatory and compliance requirements.
  • Lead root cause investigations with Engineering and Manufacturing Teams, see a CAR from open to close.
  • Perform employee training on quality procedures and processes.
  • Assist Quality Team Leader with Quality Management System gap analysis, process mapping activities and other continuous improvement projects.
  • Work with Engineering to develop/change/improve measurement methods and production processes to implement Lean practices.
  • Statistical Analysis of Manufacturing Data (SPC from ERP system).
  • Implement additional capabilities within ERP system for quality processes.
  • Conduct Internal Quality Audits as assigned. 
  • Create and maintain quality documents (control plans, QMS docs, etc.).
  • Communicate with customers and suppliers as needed.
  • Back up Quality Technician.
  • Back up Quality Assurance Specialist. 
  • Additional projects or tasks requested by Team Leader as needed.


Requirements

  • Bachelor’s Degree in Quality Engineering or relevant discipline.
  • 2-5 years’ experience in a Lean Manufacturing Environment.
  • Medical device sector experience preferred.
  • Experience with ERP Manufacturing Systems, Document Control.
  • Proficient in MS office with heavy us of word and excel.

Physical Requirements:

  • Able to stand; walk; sit; lift.; bend; reach; carry; stoop; kneel.
  • Use hand and fingers to handle, or feel objects, tools or controls; use fingers and hands to type or write; speak; or hear. 
  • To have sufficient visual acuity (with correction if necessary) to see small parts, part defects, and read computer monitors/documentation.
  • Noise level is moderate to high.
  • Able to work in conditions of high heat and humidity for several hours at a time.

Eligibility to Work:

  • Must be able to verify identity and eligibility to work in the United States and to complete the required employment eligibility verification form.
  • Must be able to pass a Background Check.