---
title: Quality Engineer at Custom Wire technologies
description: Custom Wire technologies is hiring for the Quality Engineer role in Port Washington,
  WI. Full-time role. See the full description and apply.
type: job
url: https://www.foundrole.com/jobs/quality-engineer-at-custom-wire-technologies-01a13448-fcff-7fcb-8a58-187c8aed8894
date: 2026-11-15T01:26:44Z
og_description: Join Custom Wire technologies as Quality Engineer in Port Washington, WI. Pays
  $75K–$95K per year. Full-time role.
og_image: https://www.foundrole.com/og/ld8iky.png
breadcrumbs:
  - label: Home
    url: https://www.foundrole.com/
  - label: Search
    url: https://www.foundrole.com/jobs
---

| | |
|---|---|
| **Company** | Custom Wire technologies |
| **Location** | Port Washington, WI |
| **Salary** | $75K/yr - $95K/yr |
| **Type** | Full Time |
| **Posted** | Oct 12, 2026 |

## Is this job real?

**Ghost job check:** A- · Low risk. Probably a real opening.

## Visa sponsorship

- **H-1B:** No H-1B sponsorship on record for Custom Wire technologies.
- **E-Verify:** No E-Verify enrollment on record for Custom Wire technologies.

## Pay for similar jobs

Most similar jobs pay $85,000 – $123,000 a year (median $102,000).

## Description

**Drive Quality Excellence in Medical Manufacturing**

Custom Wire Technologies (CWT) is a growing, family-owned manufacturer of precision medical components and devices. For more than 50 years, we've partnered with leading medical technology companies to produce high-quality components used in life-changing medical products.

 

We're looking for a **Quality Engineer** who enjoys solving problems, improving processes, and working closely with manufacturing teams to ensure the highest levels of product quality. If you're looking for a stable company where your work matters, your ideas are valued, and you can make a direct impact on product quality and customer satisfaction, we'd love to hear from you.

**Why Join CWT?**

- Family-owned company with nearly 25 years of success
- Stable and growing business serving the medical device industry
- Small-company environment where your contributions are recognized
- Opportunity to work on a wide variety of quality, validation, and process improvement projects
- Collaborative team culture with direct access to leadership
- Competitive benefits package, 401(k) employer contribution, and profit sharing
- Proudly located in Port Washington, Wisconsin

**Position Overview:**

Reporting to the Quality Manager, the Quality Engineer helps ensure our products and processes meet customer requirements, ISO 13485 standards, and CWT quality expectations. This role partners closely with manufacturing, engineering, and quality teams to improve processes, support product validation activities, investigate quality issues, and drive continuous improvement initiatives.

**Key Responsibilities****:**

- Lead and support equipment, process, and product validations (IQ, OQ, PQ)
- Develop, implement, and improve quality procedures and work instructions
- Program and operate vision inspection systems
- Analyze quality data and identify opportunities for process improvement
- Perform process capability studies and recommend corrective actions
- Investigate quality concerns using root cause analysis techniques
- Support corrective and preventive action activities
- Ensure compliance with ISO 13485 and company quality standards
- Collaborate with manufacturing teams to improve product quality and efficiency
- Assist with new product introductions and process development
- Support audits and quality system initiatives
- Regular physical attendance is required.

**Qualifications:**

- Bachelor of Science degree - Engineering or related field preferred, or equivalent experience.
- 3+ years related quality experience in ISO manufacturing environment; med tech and ISO 13485 experience preferred.
- Strong problem-solving and analytical skills.
- Ability to read and interpret engineering drawings and specifications.
- Proven ability to manage multiple projects and priorities.

**PREFERRED:**

- Medical device manufacturing experience
- ISO 13485 experience
- ASQ quality certification (CQE, CQT, or similar)
- Experience with Keyence or Micro Vu inspection systems.
- Statistical analysis and process capability experience
- Experience working in a job shop or custom manufacturing environment.

**Schedule:**

This position is primarily scheduled Monday through Friday during normal business hours, typically between **8:00 a.m. and 5:00 p.m.**

Occasional schedule flexibility may be required to support manufacturing operations and business needs.

**Benefits:**

CWT offers a comprehensive benefits package including:

- Medical
- Dental
- Vision
- Life and disability
- Paid Time Off
- 401(k) with employer contribution
- Profit Sharing
- Paid Holidays

**Work Authorization:**

Applicants must be authorized to work in the United States on a permanent basis. CWT does not provide employment sponsorship now or in the future.

 

 

At this time, we are not considering candidates that need any type of immigration sponsorship now or in the future to work in the United States.
## Skills

- Medical Device Manufacturing
- Quality Management System (Qms)
- Inspection
- Plant Operations
- Analytical Skills
- Quality Standards
- Technical Drawings
- Problem Solving
- Statistical Analysis
- Root Cause Analysis
- Medical Devices
- Keyence
- ISO 13485
- Process Improvement
- Continuous Improvement Process
- Statistics
- Medical Furniture
- Visual Inspection
- Process Development
- Corrective And Preventive Action (Capa)
- Master Quality Manager
- Data Validation
- Medical Technology
- New Product Introduction (Npi)
- Quality Assurance
- American Society for Quality (Asq) Certification
- Process Capability
## Benefits

- Paid Time Off (Pto)
- 401(k) Plans
- Employee Stock Options (ESOs)

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