Medical Device Quality Technician

ManpowerGroup Global, Inc.; Plymouth (MN); On-site; USD 22,000 - 25,000; Full time

Benefits offered by this job

Medical and Prescription Drug Plans

Dental Plan

Vision Plan

401(k), Plus Match

Weekly Pay

Job summary

ManpowerGroup is seeking a QA Technician I in Plymouth, MN. This onsite role focuses on maintaining product quality, reviewing DHRs, and resolving production floor issues to ensure compliance with specifications.

The candidate will support GMP documentation practices and production systems like MES, SAP, and Windchill, with 1–3 years of relevant experience and a high school diploma or GED.

Qualifications

• High School Diploma or GED required.
• 1-3 years of relevant experience in manufacturing or quality assurance.
• Knowledge of GMP and good documentation practices.
• Familiarity with production systems like MES, SAP, or Windchill.
• Ability to work under direct supervision and follow GMP guidelines.

Responsibilities

• Maintain control of product quality and manufacturing processes.
• Review Device History Records (DHR), both paper and electronic.
• Assist with resolving quality issues on the production floor and product disposition.
• Ensure all manufactured products meet applicable specifications.
• Support documentation practices and production systems such as MES, SAP, and Windchill.

Skills

GMP knowledge

Good documentation practices

Education

High School Diploma or GED

Tools

MES

SAP

Windchill

Job description

Job Title:

QA Technician I

Location:

Plymouth, MN. Onsite

Pay Range:

$16/hr - $18/hr (Depends on experience)

What's the Job?

• Maintain control of product quality and manufacturing processes
• Review Device History Records (DHR), both paper and electronic
• Assist with resolving quality issues on the production floor and product disposition
• Ensure all manufactured products meet applicable specifications
• Support documentation practices and production systems such as MES, SAP, and Windchill

What's Needed?

• High School Diploma or GED required
• 1-3 years of relevant experience in manufacturing or quality assurance
• Knowledge of GMP and good documentation practices
• Familiarity with production systems like MES, SAP, or Windchill
• Ability to work under direct supervision and follow GMP guidelines

What's in it for me?

• Opportunity to develop foundational skills in quality assurance
• Work in a collaborative and supportive environment
• Gain experience in a regulated manufacturing setting
• Potential for career growth within the organization
• Supportive team environment focused on continuous improvement

Upon completion of waiting period consultants are eligible for:

• Medical and Prescription Drug Plans
• Dental Plan
• Vision Plan
• 401(k), Plus Match
• Weekly Pay

About ManpowerGroup, Parent Company of: Manpower, Experis and Talent Solutions.