Product Engineer Visa Sponsorship Jobs in Connecticut
Connecticut's product engineer market spans insurance technology in Hartford, bioscience and medical device firms in the New Haven corridor, and advanced manufacturing along the Naugatuck Valley. Companies like Cigna, Sikorsky, and Synchrony Financial have established engineering teams that regularly hire international talent and offer visa sponsorship for qualified product engineers.
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INTRODUCTION
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in the Life
At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.
The Product Engineer II will serve as the Design Owner for commercially released Wound Management products within a high-volume manufacturing environment. This role focuses on maintaining design intent of our products following product transfer to manufacturing, including design support, yield improvement, root cause analysis, supplier collaboration, and customer return analysis. The position partners closely with Design Quality, Manufacturing, Plant Quality, Supplier Quality, and Operations to ensure our devices are safe, effective, and cost-efficient.
Key Responsibilities:
- Provide design support to manufacturing for wound management products, including support of testing methods, specifications, procedures, and troubleshooting manufacturing or test-related issues.
- Lead investigation and resolution of device specification issues, yield challenges, and production deviations to maintain high-quality output.
- Support minor device, component, or tooling redesigns, including drawing updates, to improve quality, performance, manufacturability, reliability, or cost.
- Conduct analysis of customer complaints and returned products, partnering with Design Quality and Manufacturing to identify root cause and implement corrective actions.
- Drive and support supplier-related engineering changes that affect product design, including component improvements, qualification activities, and ongoing supplier optimization efforts.
- Optimize device relative to cost, quality, risk, and performance constraints.
- Assume design responsibility for devices and/or internally produced or externally sourced components after formal transfer into high-volume production.
- Own design activities for assigned products, typically covering entire device design.
- Support investigations related to nonconformances, CAPAs, and risk assessments as needed.
- Assist customers and internal teams with device usage issues or customer testing of complex devices, as applicable.
- Partner cross-functionally with Design Quality Engineering, Manufacturing Engineering, Plant Quality Engineering, Operations, and Supply Chain to support uninterrupted production and continuous improvement initiatives.
Minimum Requirements:
- Bachelor’s degree in Engineering (Biomedical, Mechanical, Materials, Manufacturing, or related engineering discipline required).
- Bachelors degree in Engineering, plus 2 years relevant work experience, OR a Master’s degree in Engineering, with 0-2 years work experience.
Preferred Qualifications:
- Experience supporting medical devices, particularly wound management or disposable medical products.
- Hands-on experience with root cause analysis, design verification, and supplier collaboration.
- Familiarity with ISO 13485, FDA Quality System Regulations, and design control/change management processes.
- Experience analyzing customer complaints, product returns, or field issues.
- Strong communication skills with the ability to work effectively across technical and non-technical teams.
- Prior Medtronic experience.
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Join us in our mission to alleviate pain, restore health, and extend life—where your unique background and perspective are valued.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package. A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Salary ranges for U.S (excl. PR) locations (USD): $80,000.00 - $120,000.00
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week:
- Health, Dental and vision insurance
- Health Savings Account
- Healthcare Flexible Spending Account
- Life insurance
- Long-term disability leave
- Dependent daycare spending account
- Tuition assistance/reimbursement
- Simple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees:
- Incentive plans
- 401(k) plan plus employer contribution and match
- Short-term disability
- Paid time off
- Paid holidays
- Employee Stock Purchase Plan
- Employee Assistance Program
- Non-qualified Retirement Plan Supplement (subject to IRS earning minimums)
- Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
ABOUT MEDTRONIC
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.

INTRODUCTION
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in the Life
At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.
The Product Engineer II will serve as the Design Owner for commercially released Wound Management products within a high-volume manufacturing environment. This role focuses on maintaining design intent of our products following product transfer to manufacturing, including design support, yield improvement, root cause analysis, supplier collaboration, and customer return analysis. The position partners closely with Design Quality, Manufacturing, Plant Quality, Supplier Quality, and Operations to ensure our devices are safe, effective, and cost-efficient.
Key Responsibilities:
- Provide design support to manufacturing for wound management products, including support of testing methods, specifications, procedures, and troubleshooting manufacturing or test-related issues.
- Lead investigation and resolution of device specification issues, yield challenges, and production deviations to maintain high-quality output.
- Support minor device, component, or tooling redesigns, including drawing updates, to improve quality, performance, manufacturability, reliability, or cost.
- Conduct analysis of customer complaints and returned products, partnering with Design Quality and Manufacturing to identify root cause and implement corrective actions.
- Drive and support supplier-related engineering changes that affect product design, including component improvements, qualification activities, and ongoing supplier optimization efforts.
- Optimize device relative to cost, quality, risk, and performance constraints.
- Assume design responsibility for devices and/or internally produced or externally sourced components after formal transfer into high-volume production.
- Own design activities for assigned products, typically covering entire device design.
- Support investigations related to nonconformances, CAPAs, and risk assessments as needed.
- Assist customers and internal teams with device usage issues or customer testing of complex devices, as applicable.
- Partner cross-functionally with Design Quality Engineering, Manufacturing Engineering, Plant Quality Engineering, Operations, and Supply Chain to support uninterrupted production and continuous improvement initiatives.
Minimum Requirements:
- Bachelor’s degree in Engineering (Biomedical, Mechanical, Materials, Manufacturing, or related engineering discipline required).
- Bachelors degree in Engineering, plus 2 years relevant work experience, OR a Master’s degree in Engineering, with 0-2 years work experience.
Preferred Qualifications:
- Experience supporting medical devices, particularly wound management or disposable medical products.
- Hands-on experience with root cause analysis, design verification, and supplier collaboration.
- Familiarity with ISO 13485, FDA Quality System Regulations, and design control/change management processes.
- Experience analyzing customer complaints, product returns, or field issues.
- Strong communication skills with the ability to work effectively across technical and non-technical teams.
- Prior Medtronic experience.
For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.
U.S. Work Authorization & Sponsorship
At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment.
Join us in our mission to alleviate pain, restore health, and extend life—where your unique background and perspective are valued.
Benefits & Compensation
Medtronic offers a competitive Salary and flexible Benefits Package. A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
Salary ranges for U.S (excl. PR) locations (USD): $80,000.00 - $120,000.00
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
The base salary range is applicable across the United States, excluding Puerto Rico and specific locations in California. The offered rate complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and location. Compensation and benefits information pertains solely to candidates hired within the United States (local market compensation and benefits will apply for others).
The following benefits and additional compensation are available to those regular employees who work 20+ hours per week:
- Health, Dental and vision insurance
- Health Savings Account
- Healthcare Flexible Spending Account
- Life insurance
- Long-term disability leave
- Dependent daycare spending account
- Tuition assistance/reimbursement
- Simple Steps (global well-being program).
The following benefits and additional compensation are available to all regular employees:
- Incentive plans
- 401(k) plan plus employer contribution and match
- Short-term disability
- Paid time off
- Paid holidays
- Employee Stock Purchase Plan
- Employee Assistance Program
- Non-qualified Retirement Plan Supplement (subject to IRS earning minimums)
- Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums).
Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico.
Further details are available at the link below:
Medtronic benefits and compensation plans
ABOUT MEDTRONIC
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.
We are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
Product Engineer Job Roles in Connecticut
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Search Product Engineer Jobs in ConnecticutProduct Engineer Jobs in Connecticut: Frequently Asked Questions
Which companies sponsor visas for product engineers in Connecticut?
Several large employers in Connecticut have documented histories of sponsoring work visas for product engineers. These include Cigna and Aetna in Hartford's insurance technology sector, United Technologies and Sikorsky in aerospace and advanced manufacturing, and Synchrony Financial in the financial technology space. Biotech and medical device firms in the New Haven area, including Arvinas and several Yale-affiliated spinouts, also sponsor international product engineers with some regularity.
Which visa types are most common for product engineer roles in Connecticut?
The H-1B is the most common visa category for product engineers in Connecticut, as the role typically qualifies as a specialty occupation requiring a bachelor's degree or higher in engineering, computer science, or a related field. Australians may qualify for the E-3, and Canadian and Mexican nationals may pursue TN status under the USMCA. Candidates with extraordinary ability may explore the O-1A, though that requires substantial documentation of professional distinction.
How to find product engineer visa sponsorship jobs in Connecticut?
Migrate Mate filters job listings specifically by visa sponsorship willingness, making it a practical starting point for product engineers targeting Connecticut. You can narrow results by role and state to surface openings at Hartford-area insurtech firms, New Haven biotech companies, and manufacturers along the Naugatuck Valley. Because sponsorship policies differ by employer and even by hiring manager, focusing on companies with verified sponsorship histories in Connecticut saves significant time.
Which cities in Connecticut have the most product engineer sponsorship jobs?
Hartford leads Connecticut for product engineer sponsorship opportunities, driven by its concentration of large insurance and financial services employers with established international hiring programs. New Haven is a close second, anchored by Yale University's research ecosystem and a growing cluster of biotech and medical device companies. Stamford, with its proximity to New York and presence of financial services firms and tech offices, also generates product engineer openings that include visa sponsorship.
Are there state-specific considerations for product engineers seeking visa sponsorship in Connecticut?
Connecticut's prevailing wage requirements under H-1B rules are determined by the Department of Labor's Standard Occupational Classification for product engineers in each metro area. Hartford and Stamford fall into different wage tiers, so the required minimum wage an employer must offer varies by city. Connecticut's strong university pipeline, particularly from Yale, UConn, and Fairfield University, means employers here are accustomed to international candidates and some have internal immigration support teams already in place.
What is the prevailing wage for sponsored product engineer jobs in Connecticut?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.
See which product engineer employers are hiring and sponsoring visas in Connecticut right now.
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