Medical Device Quality Inspector & Process Support

Resonetics; Hudson (WI); On-site; USD 28,929 - 41,328; Full time

Job summary

Resonetics, a global leader in advanced engineering and micro manufacturing, is seeking a Quality Engineering Technician in Hudson, WI. The role focuses on inspection of final and incoming materials, documentation review, and supporting quality initiatives in a fast-paced environment.

Responsibilities include processing nonconformances, maintaining control plans, supporting Gage R&R, and driving continuous improvement projects while upholding ISO 13485 and FDA compliance awareness.

Qualifications

• High school diploma or equivalent.
• Minimum 1 year experience with operating manufacturing and/or test equipment.
• Demonstrated strong communication skills.

Responsibilities

• Inspecting final documentation packages.
• Conducting incoming inspection of raw material.
• Managing the flow of finished goods to shipping.
• Coordinating timely processing of Nonconformances, Process Deviations, and other quality records.
• Control and organization of the quarantine hold area.
• Support maintaining control plans/pFMEAs.
• Supporting document control activities.
• Supporting Gage R&R facilitation.
• Supporting Corrective and Preventive Actions.
• Supporting continuous improvement projects.
• Assisting with troubleshooting of production processes.
• Revising quality procedures.
• Conducting training, including onboarding of new employees.

Skills

Strong communication skills

Quality inspection

Problem solving

Education

High school diploma or equivalent

Associate degree or equivalent

Tools

Gage R&R

Process validation tools

Job description

Resonetics, a global leader in advanced engineering and micro manufacturing, is seeking a Quality Engineering Technician in Hudson, WI. The role focuses on inspection of final and incoming materials, documentation review, and supporting quality initiatives in a fast-paced environment.

Responsibilities include processing nonconformances, maintaining control plans, supporting Gage R&R, and driving continuous improvement projects while upholding ISO 13485 and FDA compliance awareness.