CPT Product Engineering Manager Jobs
Product Engineering Manager jobs on CPT place you at the intersection of technical leadership and organizational responsibility, roles your DSO must confirm are directly tied to your enrolled program. Expect full-time authorization requirements, clear deliverable scopes in your CPT agreement, and employers who file Labor Condition Applications before your start date.
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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 JobsProduct Engineering Manager CPT: Frequently Asked Questions
Does a Product Engineering Manager role qualify for CPT authorization?
Yes, if your academic program directly covers product management, engineering leadership, or technology strategy. Your DSO will review whether the job duties, overseeing engineering teams, setting technical roadmaps, coordinating releases, constitute an integral part of your curriculum. Programs in computer science, systems engineering, MBA with a technology concentration, and similar fields typically support this authorization.
Can I work full-time as a Product Engineering Manager on CPT?
Full-time CPT is permitted, but using 12 or more months of full-time CPT eliminates your eligibility for OPT after graduation. Many F-1 students in management roles structure their CPT as part-time during the academic term and switch to full-time during breaks. Coordinate the timing carefully with your DSO before accepting an offer that requires full-time availability from day one.
How do I find employers actively hiring F-1 CPT students for engineering manager roles?
Search Migrate Mate to identify employers with verified LCA filing history for engineering manager positions. Companies that have filed LCAs for this occupation code have already navigated the DOL certification process, which means they're familiar with the legal and HR steps involved in authorizing and eventually sponsoring F-1 students, reducing friction for your CPT onboarding.
What happens to my CPT authorization if my role transitions mid-internship?
If your responsibilities shift significantly, for example, from an individual contributor track to a full people-management scope, your original CPT authorization may no longer accurately describe your duties. You'll need to return to your DSO and request an updated CPT authorization reflecting the new role. Starting expanded responsibilities before your DSO issues the updated I-20 puts your F-1 status at risk.
Does CPT experience as a Product Engineering Manager strengthen my H-1B petition later?
Yes. Documented CPT employment in a specialty occupation like product engineering management establishes a concrete work history in the role, which directly supports the specialty occupation argument in a future H-1B visa petition. Your employer can reference the CPT period when describing your qualifications, your demonstrated performance, and the company's ongoing need for someone with your specific degree and experience combination.