Medical Device Quality Technician

ManpowerGroup; 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 for an onsite role supporting production and quality control teams. The position requires a High School Diploma or GED and 1-3 years of manufacturing or QA experience, with GMP familiarity.

Responsibilities include reviewing DHRs and ensuring specifications are met. The role offers an opportunity to develop foundational QA skills in a regulated manufacturing environment, with a collaborative team and potential for growth.

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 MES, SAP, or Windchill.

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

Attention to detail

Communication skills

Proactive attitude

Education

High School Diploma or GED

Tools

MES

SAP

Windchill

Job description

Our client, a leading organization in the manufacturing industry, is seeking a QA Technician I to join their team. As a QA Technician I, you will be part of the Quality Assurance department supporting production and quality control teams. The ideal candidate will demonstrate attention to detail, strong communication skills, and a proactive attitude, which will align successfully in the organization.

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.

ManpowerGroup is committed to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup and all of its subsidiaries to recruit, train, promote, transfer, pay and take all employment actions without regard to an employee's race, color, national origin, ancestry, sex, sexual orientation, gender identity, genetic information, religion, age, disability, protected veteran status, or any other basis protected by applicable law.