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New · posted Oct 20

Eptam West · Medical Devices

Quality Engineer

  • Lakeville, MN
  • On-site
  • Full-time
  • Senior & Principal
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Deadline

Open until filled

The role

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.

What you need

  • 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: 4+ 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.

ADP1573

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

What you'll do

OTHER RESPONSIBILITIES

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

Pay and benefits

Eptam West didn't publish pay for this role

See what similar roles pay on Regulatory Jobs, or try the salary calculator.

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)

Where you'll work

Lakeville, MNOn-siteOpen in Maps (opens in a new tab)

More jobs in Lakeville, MN

Schedule and working conditions

Days

Hours

Shift5 days a week8.5-hour shifts42.5 hours on site a week

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.
  • 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.
Equal opportunity, accessibility and legal noticesEptam West's statements, word for word

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

Job intelligence

The context around this role

Live data · October 20, 2026

Salary intelligence

How the pay compares

Senior & Principal roles in Minnesota19 roles publishing pay

Middle half $92,000 to $111,750, median $99,000

Senior & Principal roles in the US302 roles publishing pay

Middle half $102,625 to $137,500, median $120,250
Annual base pay
Annual base payLowMedianHigh
Minnesota$92,000$99,000$111,750
All US$102,625$120,250$137,500

Comparisons: the base pay employers published on open Quality Assurance roles at the same level on Regulatory Jobs, October 20, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Quality Assurance

The general path across 895 open Quality Assurance roles on Regulatory Jobs, with the titles they carry most. Not Eptam West's own promotion track.

  1. One step back

    Associate & Specialist

    Often: Quality Engineer · Quality Technician

    $81K median243 open
  2. This role

    Senior & Principal

    Often: Quality Engineer · Senior Quality Engineer

    $120K median381 open
  3. Next step

    Manager

    Often: Manager, Quality Assurance · Quality Manager

    $155K median138 open
  4. Later

    Director

    Often: Director, Quality · Associate Director, Quality Assurance

    $209K median118 open
  5. Later

    VP & Executive

    Often: AVP · Executive Director Quality, Cell & Gene Therapy

    $302K median15 open

Skills DNA

What this role leans on

How many of the posting's 17 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 2 linesQuality systems and risk: 3 linesData and digital systems: 1 lineCollaboration and leadership: 6 linesGMPQuality systemsData systemsTeamwork
  • Collaboration and leadership6
  • Quality systems and risk3
  • GMP and compliance2
  • Data and digital systems1

Company hiring pulse

Eptam West on Regulatory Jobs

3
Open roles
3
Distinct roles
3
Locations

By discipline

  • Quality3 100%

By level

  • Associate & Specialist2 67%
  • Senior & Principal1 33%
See all 3 Eptam West roles

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Quality Engineer at Eptam West

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