Quality Engineer III

Experis Technology Group; Saint Paul (MN); On-site; USD 52,000 - 72,000; Full time

Job summary

Experis Technology Group in Saint Paul, MN seeks a Quality Engineer III for a 12-month, 100% onsite assignment. The role focuses on integrating quality processes for medical devices, with pay of $45/hour on W2.

You will support regulatory compliance (FDA/ISO 13485, 14971), risk management, and documentation such as VMPs, DIRA, and inspection plans, while helping write SOPs and training.

Qualifications

• 3–5 years experience in quality or related field.
• 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.

Skills

3–5 years experience

Medical Device Quality experience

FDA/ISO regulations knowledge

Ability to ramp up quickly

Job description

Title: Quality Engineer III

Location: Saint Paul, MN

Duration: 12Months

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.