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ManpowerGroup is seeking a Quality Engineer III for a 12-month, on-site assignment in Saint Paul, MN. The role focuses on supporting medical device quality activities and ensuring compliance with FDA/ISO 13485 and 14971 requirements.
You will perform acceptance testing, develop and review validation master plans, conduct hazard analyses, and assist with SOPs, training, and test protocol execution as needed.
Title: Quality Engineer III
Location: Saint Paul, MN
Duration: 12 Months
100% Onsite
Pay: $45/hr W2
Qualifications:
3-5 years experience
Medical Device Quality experience (Ops or Manufacturing)
Strong working knowledge of FDA/ISO regulations (13485, 14971, etc.)
Ability to ramp up quickly
Responsibilities:
Support Quality integration activities including:
Acceptance Activities and Inspection Plans
Data Integrity Risk Assessments (DIRA)
Validation Master Plans (VMPs)
Hazard Analysis activities
Assist with SOPs, Work Instructions, and occasional training
Occasionally write/execute test protocols and report.
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.