CPT QA Engineer Jobs
QA Engineer roles qualify for CPT when the work is directly tied to your degree program in computer science, software engineering, or a related field. Your DSO must authorize each position before you start. Roles involving test automation, defect tracking, and software validation align closely with technical degree curricula and typically meet CPT's integral-part requirement.
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Get Access To All JobsRequisition ID:
67404
Title:
Engineering Co-op - Quality Assurance - Product Surveillance
Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a student pursuing an engineering degree to support the Product Surveillance team in Naples, FL. The Product Surveillance team is responsible for the intake, documentation, investigation, reporting, and trending of product quality complaints to support product safety, quality, and regulatory compliance. With the support of fellow team members, the successful candidate will assist with the intake, documentation, evaluation, investigation, and trending of product quality complaints. Responsibilities include performing complaint investigations, conducting data analysis and trending activities, preparing technical reports, and supporting engineering projects related to product performance and quality. The ideal candidate will demonstrate strong attention to detail, organizational skills, and the ability to accurately document findings while working within established procedures and regulatory requirements. The individual will be expected to manage assigned tasks effectively, communicate findings and issues in a timely manner, and contribute to the continuous improvement of complaint handling and product surveillance processes. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.
This co-op will run from January 2027 – June 2027. The ideal candidate will have the availability to work 40 hours per week at our Naples, FL facility.
Main Objective:
To support the Product Surveillance team with medical device complaint handling, investigation, and data analysis.
Essential Duties and 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 as appropriate.
- 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.
Education and Experience:
Enrolled as a full-time student pursuing a bachelor's degree in engineering or engineering technology, or a recent engineering or engineering technology graduate, required. Junior or above, studying Mechanical or Biomedical Engineering preferred.
(Recent graduates must be within six months of their graduation date to qualify.)
Knowledge and Skill Requirements/Specialized Courses and/or Training:
- Ability to effectively communicate, oral and written, and possess the ability to work through technical issues.
- Knowledge of Regulatory and ISO guidelines pertaining to medical devices preferred.
- Basic knowledge of product risk management, CAPA, and Nonconformance Reporting (NCR) preferred.
- Knowledge of orthopedic medical devices (implant, instruments, biologics, etc) preferred.
Machine, Tools, and/or Equipment Skills:
PC; Familiarity with Microsoft Office Suite preferred.
Arthrex Benefits are:
- Medical Insurance (if 25 or more hours per week), including access to telehealth services
- Employee Assistance Program (EAP)
- Free Onsite Medical Clinics
- Free Onsite Lunch
- Volunteer PTO (8 hours)
- Access to the Wellness Center (For South West Florida positions only)
All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law.
Requisition ID:
67404
Title:
Engineering Co-op - Quality Assurance - Product Surveillance
Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a student pursuing an engineering degree to support the Product Surveillance team in Naples, FL. The Product Surveillance team is responsible for the intake, documentation, investigation, reporting, and trending of product quality complaints to support product safety, quality, and regulatory compliance. With the support of fellow team members, the successful candidate will assist with the intake, documentation, evaluation, investigation, and trending of product quality complaints. Responsibilities include performing complaint investigations, conducting data analysis and trending activities, preparing technical reports, and supporting engineering projects related to product performance and quality. The ideal candidate will demonstrate strong attention to detail, organizational skills, and the ability to accurately document findings while working within established procedures and regulatory requirements. The individual will be expected to manage assigned tasks effectively, communicate findings and issues in a timely manner, and contribute to the continuous improvement of complaint handling and product surveillance processes. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.
This co-op will run from January 2027 – June 2027. The ideal candidate will have the availability to work 40 hours per week at our Naples, FL facility.
Main Objective:
To support the Product Surveillance team with medical device complaint handling, investigation, and data analysis.
Essential Duties and 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 as appropriate.
- 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.
Education and Experience:
Enrolled as a full-time student pursuing a bachelor's degree in engineering or engineering technology, or a recent engineering or engineering technology graduate, required. Junior or above, studying Mechanical or Biomedical Engineering preferred.
(Recent graduates must be within six months of their graduation date to qualify.)
Knowledge and Skill Requirements/Specialized Courses and/or Training:
- Ability to effectively communicate, oral and written, and possess the ability to work through technical issues.
- Knowledge of Regulatory and ISO guidelines pertaining to medical devices preferred.
- Basic knowledge of product risk management, CAPA, and Nonconformance Reporting (NCR) preferred.
- Knowledge of orthopedic medical devices (implant, instruments, biologics, etc) preferred.
Machine, Tools, and/or Equipment Skills:
PC; Familiarity with Microsoft Office Suite preferred.
Arthrex Benefits are:
- Medical Insurance (if 25 or more hours per week), including access to telehealth services
- Employee Assistance Program (EAP)
- Free Onsite Medical Clinics
- Free Onsite Lunch
- Volunteer PTO (8 hours)
- Access to the Wellness Center (For South West Florida positions only)
All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other status protected by law.
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Get Access To All JobsQA Engineer CPT: Frequently Asked Questions
Does a QA Engineer role qualify for CPT?
Yes, if the work is an integral part of your degree program and your school offers a course or practicum tied to it. Roles involving software testing, test automation, defect management, or quality assurance processes align well with computer science, software engineering, and information systems curricula. Your DSO makes the final determination based on your specific program requirements and the employer's job description.
Can I work as a QA Engineer on CPT before completing my first year of F-1 study?
No. F-1 students must complete one full academic year before becoming eligible for CPT. This is a USCIS requirement, not a school policy, so no DSO can waive it. If you receive a QA Engineer offer before your first year ends, the earliest your CPT authorization can begin is the first day after your one-year mark.
What documents does a QA Engineer CPT employer need from me?
Your employer needs your updated I-20 showing the CPT authorization on page two, with the correct employer name, start date, and end date listed. They also need your passport, F-1 visa stamp, and I-94 arrival record for I-9 verification. Some employers with E-Verify accounts will run your documents through the system on day one, which is standard practice and not a problem for F-1 CPT workers.
How do I find QA Engineer employers that understand F-1 CPT?
Search for employers with existing DOL Labor Condition Application filings for software quality or testing roles on Migrate Mate. Companies that have already navigated work authorization paperwork are significantly less likely to rescind offers when you present your CPT I-20. Avoid applying to employers advertising that they cannot provide any immigration support, as even CPT requires basic I-9 familiarity from the hiring team.
Does QA Engineer CPT count toward STEM OPT eligibility?
CPT itself doesn't directly qualify you for STEM OPT, but your degree does. If you graduate with a STEM-designated degree and your QA Engineer role falls under an eligible SOC code, such as Software Quality Assurance Analysts and Testers, you can apply for the 24-month STEM OPT extension after your initial 12-month OPT period. Confirm your program's STEM designation with your DSO before graduation.