CPT Quality Assurance Analyst Jobs
Quality Assurance Analyst CPT jobs let F-1 students apply software testing, defect tracking, and process validation skills in a paid role that counts toward your degree. Your DSO must authorize CPT before your start date, and the work must connect directly to your program of study.
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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 JobsQuality Assurance Analyst CPT: Frequently Asked Questions
Does a Quality Assurance Analyst role qualify for CPT authorization?
Yes, if the work directly relates to your field of study. QA Analyst duties like test planning, defect analysis, and process documentation connect clearly to degrees in computer science, information systems, or software engineering. Your DSO makes the final determination, so bring a detailed job description that maps specific duties to courses in your program.
Can I do CPT as a Quality Assurance Analyst while attending school full time?
Part-time CPT, defined as 20 hours or fewer per week, doesn't affect your full-time enrollment requirement. Full-time CPT, more than 20 hours per week, is permitted but eliminates one semester of OPT eligibility for every 12 months used. Most F-1 students in QA roles choose part-time CPT during the academic year to protect their OPT.
How do I find Quality Assurance Analyst employers who hire CPT students?
Migrate Mate lets you filter QA Analyst openings by employers with a track record of hiring F-1 students and filing Labor Condition Applications for technical roles. Focusing on companies with existing LCA filings in software quality or systems testing reduces the time spent explaining your work authorization status to HR teams unfamiliar with CPT.
What documents do I need to start a CPT Quality Assurance Analyst job?
You need an updated I-20 with CPT authorization endorsed by your DSO, issued before your start date. You'll also need the employer's offer letter specifying your role title, start and end dates, weekly hours, and work location. Remote or hybrid QA roles must list the employer's physical address, not your home address, as the work site on your I-20.
Does CPT experience as a QA Analyst count toward H-1B specialty occupation requirements?
CPT work experience in a QA Analyst role is counted the same as any other professional work experience by USCIS. If your employer later files an H-1B visa petition for you, they'll reference your QA duties to demonstrate the role meets specialty occupation standards, typically a position requiring at least a bachelor's degree in a directly related technical field.