---
title: Quality Engineer 1st Shift at EPTAM Precision Solutions
description: EPTAM Precision Solutions is hiring for the Quality Engineer 1st Shift role in
  Lakeville, MN. Part-time role. See the full description and apply.
type: job
url: https://www.foundrole.com/jobs/quality-engineer-1st-shift-at-eptam-precision-solutions-01a154a1-a59d-731d-b34b-438b9de676df
date: 2026-11-15T01:26:44Z
og_description: Join EPTAM Precision Solutions as Quality Engineer 1st Shift in Lakeville, MN.
  Pays $65K–$72K per hour. Part-time role.
og_image: https://www.foundrole.com/og/haljqf.png
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---

| | |
|---|---|
| **Company** | EPTAM Precision Solutions |
| **Location** | Lakeville, MN |
| **Salary** | $65K/hr - $72K/hr |
| **Type** | Part Time |
| **Posted** | Nov 02, 2026 |

## Is this job real?

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

## Visa sponsorship

- **H-1B:** EPTAM Precision Solutions sponsors H-1B visas. It filed 1 H-1B petition (FY2026 Q1 – FY2026 Q4).
- **E-Verify:** No E-Verify enrollment on record for EPTAM Precision Solutions.

## Pay for similar jobs

Most similar jobs pay $76,000 – $102,000 a year (median $85,000).

## Description

**EPTAM Precision Micro-Machining** is looking for a **Quality Engineer** **– 1st Shift** to join our team in **Lakeville, MN**. Join us as we create medical devices that support our OEM partners in creating life-saving parts and positive outcomes for their patients.

**EPTAM Precision Micro-Machining** in is a world-class manufacturer specializing in precision manufacturing of custom medical device components for original device manufacturers. We've established a strong reputation in providing custom implantable components across various medical sectors, including orthopedic, orthopedic spine, cardiovascular, vascular, endovascular, and pelvic health sectors. Our manufacturing operations support the Robot Assisted Surgery (RAS) and Minimally Invasive Surgery (MIS) industries, as OEM’s look for partners for the future of advanced interventions.

Our facility, compliant with FDA and ISO 13485 standards, is celebrated for its high-quality system and standards. Our ingrained culture of quality, combined with seamless collaboration between Engineering, Quality, and Manufacturing Operations, allows us to deliver the very best to our employees, customers, and the world.

**EPTAM Solutions**, our parent company with locations nationwide, is at the Heart of Manufacturing. We recognize our parts touch lives, and our teams assume this responsibility with vigor. Our minds never sleep. Join our incredible team at any one of our locations and reap the benefits of an employee focused company. We excel at what we do for our customers, our employees, and the world.

**Benefits Include:**

- Professional Development/On the Job Training
- Health and Wellness Benefits
- Clean, Friendly, Safe work Environment
- Recognition and Rewards Program
- Tuition Re-imbursement
- Competitive Pay/Merit Increases
- 401k w/ Company Match
- Employee Assistance Program (EAP)

**SHIFT DETAILS:**

**1st** **Shift**

Monday through Friday 6:00am to 2:30pm

**POSITION SUMMARY:** The **Quality Engineer** is primarily for the following:

- Assisting with monitoring and maintaining the Quality Management System (QMS) to ensure compliance with ISO 13485 and 21 CFR part 820 (Quality System Regulation).
- Providing focused, Quality Engineering support via communication to department managers of the Quality Management System including Complaint, CAPA, Risk Management, Supplier Quality and Document Control processes.

**ESSENTIAL FUNCTIONS:** *Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.*

- Ensure Quality Management System documentation and reporting of all Quality-related issues and projects are maintained.
- Identify and support Quality Manager by executing plans and actions to achieve assigned quality goals.
- Coordinate the tracking and closure of Quality issue-related documentation and Change Control related to RMA, NC, CAPA, and MRB System.
- Support process owners and department managers/value stream leaders in methods of process improvement and process control related to RMA, NC, CAPA, and other Quality Management issues or concerns.
- Monitor customer requests and ensure successful execution of customer-driven acceptance activities.
- Develop, vet, and maintain inspection plans.
- Draft IQ, OQ, and PQ protocols, execute validations within work cell(s), and write validation reports (IQ/OQ/PQ) for equipment and processes.
- Measure components utilizing advanced measuring equipment (i.e., CMM, vision systems, etc.) and various hand gages such as calipers and micrometers.
- Employees must be able to relate to other people beyond receiving instructions. Can get along with co-workers or peers and respond appropriately to feedback from a supervisor in a professional manner.

**OTHER RESPONSIBILITIES:**

- Represent the company, as required, during customer, internal and ISO audits, as well as FDA inspections.
- Support communication that ensures management and employee understanding of current Good Manufacturing Practices (cGMP).
- Leverage industry practices and apply to internal systems and processes.
- Ensure quality requirement flow down of customer purchase orders for products to be manufactured.
- Identify quality system needs and convey same to Quality Manager for strategic planning and budgeting purposes.
- Implement statistical process analysis on new and existing products as needed.
- Identify, suggest, and lead changes to benefit the organization within the Quality System or Production.
- Understand the sensitivity of the data handled by systems under your control and take appropriate measures to protect it.

**EDUCATION AND EXPERIENCE:**

- **EDUCATION:** High School diploma or general education degree (GED). Bachelor’s degree with a major in a relevant technical field (STEM) preferred, but not required.
- **EXPERIENCE**: 1+ year(s) relevant quality assurance experience or training, equivalent combinations or education and experience accepted OR demonstrated ability to execute the Essential Functions for this position. Internships and PT experience acceptable. Experience within a manufacturing, medical device company or other similarly regulated manufacturing environment preferred.
- **LICENSES, CERTIFICATIONS AND/ REGISTRATIONS**: Industry recognized Quality certification(s) preferred, but not required.

ADP1550

1st Shift  
Monday through Friday 6:00am to 2:30pm
## Skills

- Quality Management System (Qms)
- Inspection
- Value Stream Mapping
- FindLaw Code of Federal Regulations CFR
- Good Manufacturing Practices
- Risk Management
- Quality Engineering
- Material Review Board
- Process Analysis
- Supplier Quality Management
- Purchase Order Management
- Medical Devices
- ISO 13485
- Process Improvement
- Quality Management
- Micrometers
- Strategic Planning
- Document Control
- Change Control
- Quality Assurance Procedures
- Corrective And Preventive Action (Capa)
- Master Quality Manager
- Data Validation
- Quality System Regulation (Fda Qsr)
- Technical Documentation
- ISO Audit
- Quality Assurance
- Precision Measuring Instruments
- Communication
- Process Control
- Equities
- Budgeting
- Calipers
## Benefits

- Professional Development
- Mental Health
- 401(k) Plans

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