QA Engineering Co-op: Product Surveillance

Arthrex GmbH; Naples (FL); On-site; USD 25,000 - 30,000; Full time

Benefits offered by this job

Medical Insurance (if 25+ hrs)

Employee Assistance Program (EAP)

Free Onsite Medical Clinics

Free Onsite Lunch

Wellness Center access

Job summary

Arthrex, Inc. in Naples, FL is seeking an Engineering Co-op to support the Product Surveillance team in complaint handling, investigation, and data analysis.

The role offers hands-on experience in data gathering and trending within a regulated medical device environment, with collaboration across design, manufacturing and quality engineering functions. A 2027 January–June schedule requires 40 hours per week.

Qualifications

• Enrolled as a full-time student pursuing a bachelor's degree in engineering or engineering technology.
• Junior or above; recent graduates within six months of graduation.
• Mechanical or Biomedical Engineering preferred.

Responsibilities

• Receive and analyze previous complaint data and leverage for future investigations.
• Assist with data gathering and analytics for monthly complaint trending activities.
• Perform root cause analysis for returned complaint devices or identified trends.
• Support global complaint triage, intake, evaluation, reporting, investigation, closure and trending activities.
• Partner with design, manufacturing and quality engineers as well as product management teams to drive continuous process and product improvement.
• Review of Supplier Quality Agreements and incorporation of information into electronic complaint system.
• Other duties as assigned.

Skills

Communication

Regulatory knowledge

CAPA & NCR knowledge

Orthopedic devices knowledge

Education

Engineering degree (BEng/BE or BSE)

Tools

Microsoft Office

Job description

Arthrex, Inc. in Naples, FL is seeking an Engineering Co-op to support the Product Surveillance team in complaint handling, investigation, and data analysis.

The role offers hands-on experience in data gathering and trending within a regulated medical device environment, with collaboration across design, manufacturing and quality engineering functions. A 2027 January–June schedule requires 40 hours per week.