Medical Device Quality Engineer Co-op

Resonetics; New Chicago (OH); On-site; USD 32,000 - 39,000; Full time

Job summary

Resonetics is seeking a Quality Engineering Co-op in the United States to support quality systems, data analysis, and continuous improvement in regulated medical-device manufacturing. Gain hands-on experience with investigations, process validation, and documentation while collaborating with cross-functional teams.

You will assist with nonconforming material investigations, data trending, and internal audit prep, and work with Engineering and Operations to drive root-cause analysis and

Qualifications

• Current enrollment in a bachelor’s degree program in Quality, Mechanical, Manufacturing, Biomedical, Industrial, or a related Engineering discipline.
• Strong analytical skills and exceptional attention to detail.
• Interest in regulated manufacturing and medical-device quality systems.
• Working knowledge of Microsoft Excel and the ability to clearly document technical information.

Responsibilities

• Assist with investigations related to nonconforming material, customer feedback, corrective actions, and process deviations.
• Support quality data collection, trending, and reporting to identify improvement opportunities.
• Help maintain quality records, inspection documentation, and controlled procedures.
• Participate in process-validation and qualification activities, including collection and review of supporting data.
• Work with Engineering and Operations to support root-cause analysis and implementation of corrective actions.
• Assist with internal audit preparation and other quality-system activities as needed.
• Other duties as assigned.

Skills

Analytical skills

Attention to detail

Regulated manufacturing

Excel

Documentation

Education

Bachelor's degree in Quality, Mechanical, Manufacturing, Biomedical, Industrial or related Engineering

Job description

Resonetics is seeking a Quality Engineering Co-op in the United States to support quality systems, data analysis, and continuous improvement in regulated medical-device manufacturing. Gain hands-on experience with investigations, process validation, and documentation while collaborating with cross-functional teams.

You will assist with nonconforming material investigations, data trending, and internal audit prep, and work with Engineering and Operations to drive root-cause analysis and