Software Design Engineer Visa Sponsorship Jobs in New Jersey
Software design engineer roles in New Jersey sit at the center of a dense tech corridor spanning Jersey City, Newark, and Princeton. Major employers including Johnson & Johnson, Cognizant, and Siemens have established engineering teams across the state. International candidates will find active H-1B visa sponsorship across enterprise software, life sciences technology, and financial systems.
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Get Access To All JobsWhy Orthofix?
Guided by our organizational values – Take Ownership | Innovate Boldly | Win Together – we collaborate closely with world-class surgeons and other partners to improve people’s quality of life. At Orthofix, we want team members who build relationships and share knowledge, challenge the status quo, and deliver results every day to help us achieve our vision to be the unrivaled partner in Med Tech.
Our global team of over 1,600 employees brings to market highly innovative, cost-effective, and user-friendly medical technologies that heal musculoskeletal pathologies for patients and the healthcare professionals who treat them. Looking to change people’s lives? Look no further.
We offer an interesting opportunity to join our Quality Engineering team, based in Bussolengo (VR) as Sr. Quality Engineer, Design Assurance, reporting to the Quality Engineering Manager, on a full-time contract.
As part of the Quality Team, you will be responsible for liaising between Quality Compliance, Quality Management System, Research & Development (R&D) Area and Regulatory Affairs Area during the Design & Development phase of products and their complete lifecycle, including post-market surveillance and design changes.
You will guarantee that Design & Development activities are conducted in compliance with internal procedures and in conformity with standards, directives and laws applicable to the Organization. You will work in contact with Design & Development Area coordinating specific activities like Risk Management process, design validation, usability and final release.
What will your contribution be?
- Manage (i.e. promote, coordinate and document) the Risk Management activities during the Product Development Process, in relation to product modifications and during post-marketing surveillance.
- Manage (promote, coordinate and document), in cooperation with R&D, Marketing, Medical Science and Clinical Evidence, the usability and design validation about new products, including participation to simulated use testing activities.
- Cooperate with internal departments during the Product Development Process to regulatory release (CE Mark, FDA approval) for:
- new products (standard products, small series, custom products);
- product modifications.
- Support Quality Compliance and Clinical evidence areas in the Post-Market Surveillance activities providing contribution to complaints analysis, PSUR, PMCF report and CER in relation to risk analysis, design validation and applicable standards.
- Cooperate with Regulatory Affairs Area to prepare regulatory submissions (e.g. 510K pre-market notifications), support all the regulatory pre- and post-market activities related to technical aspects and prepare the Technical File documentation.
- Support the R&D Area to formalize:
- Product requirements definition and review;
- Project development plan;
- Produce development phase gate documentation;
- Design verification documentation.
- Implement and update internal procedures relevant to the above mentioned activities.
- Support the preparation and review of product technical & marketing sheets.
- Travel may be needed (10%-15%).
What are we looking for?
- Preferred technical degree or master’s degree.
- A previous experience of at least 3 years in a similar role is required, preferably in a regulated industry (medical device).
- Advanced knowledge of English and Italian.
- Methodical and critical thinking.
- Excellent organizational and project management skills.
- Problem solving skills and proactivity.
- Ability to work according to procedures, rules and regulations.
- Adherence to timelines and result-oriented attitude.
- Precision and attention to detail.
- Analytical approach to resolve complex issues.
- Ability to work in team and autonomously.
- Accountability for the assigned tasks.
- Knowledge of relevant regulations (European MDD, MDR, FDA Guidances, ISO 13485, ISO 14971, EN 62366, IEC 62304, IEC 6061, etc.).
- Knowledge of relevant standards and application regarding biocompatibility, sterilization, reprocessing and cleaning.
What soft skills will you improve?
- Ability to work precisely according to procedures, rules, and regulations.
- Analytical mindset, attention to detail, and ability to manage multiple priorities.
- Good interpersonal skills and ability to work in cross-functional teams.
- Adherence to timelines and result-oriented attitude.
- Orderliness and attention to detail.
- Accountability for the assigned tasks.
What will you find?
- Friendly, warm, and innovative atmosphere.
- Healthy, inspiring, and international and inclusive work environment.
- Training and development opportunities.
- Smart working model (two days per week).
- Competitive reward packages.
- Social and company events.
- Wellbeing initiatives (welfare).
- Canteen.
- Benefits (Pension Fund - Health Insurance).
- Working Hours: 8:30-17:30 Monday to Thursday and 8:30-16:30 Friday.
What we offer?
- This is a full-time job.
- The contract is a permanent contract.
- Salary package range: 40,000/43,000 euro*.
- The package will be evaluated based on the experience of the person.
Do you want to join us? Are you ready to make a difference?
We look forward to receiving your application.
Why Orthofix?
Guided by our organizational values – Take Ownership | Innovate Boldly | Win Together – we collaborate closely with world-class surgeons and other partners to improve people’s quality of life. At Orthofix, we want team members who build relationships and share knowledge, challenge the status quo, and deliver results every day to help us achieve our vision to be the unrivaled partner in Med Tech.
Our global team of over 1,600 employees brings to market highly innovative, cost-effective, and user-friendly medical technologies that heal musculoskeletal pathologies for patients and the healthcare professionals who treat them. Looking to change people’s lives? Look no further.
We offer an interesting opportunity to join our Quality Engineering team, based in Bussolengo (VR) as Sr. Quality Engineer, Design Assurance, reporting to the Quality Engineering Manager, on a full-time contract.
As part of the Quality Team, you will be responsible for liaising between Quality Compliance, Quality Management System, Research & Development (R&D) Area and Regulatory Affairs Area during the Design & Development phase of products and their complete lifecycle, including post-market surveillance and design changes.
You will guarantee that Design & Development activities are conducted in compliance with internal procedures and in conformity with standards, directives and laws applicable to the Organization. You will work in contact with Design & Development Area coordinating specific activities like Risk Management process, design validation, usability and final release.
What will your contribution be?
- Manage (i.e. promote, coordinate and document) the Risk Management activities during the Product Development Process, in relation to product modifications and during post-marketing surveillance.
- Manage (promote, coordinate and document), in cooperation with R&D, Marketing, Medical Science and Clinical Evidence, the usability and design validation about new products, including participation to simulated use testing activities.
- Cooperate with internal departments during the Product Development Process to regulatory release (CE Mark, FDA approval) for:
- new products (standard products, small series, custom products);
- product modifications.
- Support Quality Compliance and Clinical evidence areas in the Post-Market Surveillance activities providing contribution to complaints analysis, PSUR, PMCF report and CER in relation to risk analysis, design validation and applicable standards.
- Cooperate with Regulatory Affairs Area to prepare regulatory submissions (e.g. 510K pre-market notifications), support all the regulatory pre- and post-market activities related to technical aspects and prepare the Technical File documentation.
- Support the R&D Area to formalize:
- Product requirements definition and review;
- Project development plan;
- Produce development phase gate documentation;
- Design verification documentation.
- Implement and update internal procedures relevant to the above mentioned activities.
- Support the preparation and review of product technical & marketing sheets.
- Travel may be needed (10%-15%).
What are we looking for?
- Preferred technical degree or master’s degree.
- A previous experience of at least 3 years in a similar role is required, preferably in a regulated industry (medical device).
- Advanced knowledge of English and Italian.
- Methodical and critical thinking.
- Excellent organizational and project management skills.
- Problem solving skills and proactivity.
- Ability to work according to procedures, rules and regulations.
- Adherence to timelines and result-oriented attitude.
- Precision and attention to detail.
- Analytical approach to resolve complex issues.
- Ability to work in team and autonomously.
- Accountability for the assigned tasks.
- Knowledge of relevant regulations (European MDD, MDR, FDA Guidances, ISO 13485, ISO 14971, EN 62366, IEC 62304, IEC 6061, etc.).
- Knowledge of relevant standards and application regarding biocompatibility, sterilization, reprocessing and cleaning.
What soft skills will you improve?
- Ability to work precisely according to procedures, rules, and regulations.
- Analytical mindset, attention to detail, and ability to manage multiple priorities.
- Good interpersonal skills and ability to work in cross-functional teams.
- Adherence to timelines and result-oriented attitude.
- Orderliness and attention to detail.
- Accountability for the assigned tasks.
What will you find?
- Friendly, warm, and innovative atmosphere.
- Healthy, inspiring, and international and inclusive work environment.
- Training and development opportunities.
- Smart working model (two days per week).
- Competitive reward packages.
- Social and company events.
- Wellbeing initiatives (welfare).
- Canteen.
- Benefits (Pension Fund - Health Insurance).
- Working Hours: 8:30-17:30 Monday to Thursday and 8:30-16:30 Friday.
What we offer?
- This is a full-time job.
- The contract is a permanent contract.
- Salary package range: 40,000/43,000 euro*.
- The package will be evaluated based on the experience of the person.
Do you want to join us? Are you ready to make a difference?
We look forward to receiving your application.
Software Design Engineer Job Roles in New Jersey
See all 303+ Software Design Engineer Jobs in New Jersey
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Search Software Design Engineer Jobs in New JerseySoftware Design Engineer Jobs in New Jersey: Frequently Asked Questions
Which companies in New Jersey sponsor visas for software design engineers?
Large employers with established sponsorship track records in New Jersey include Cognizant, Johnson & Johnson, Siemens, Conduent, and Synchronoss Technologies. Financial services firms along the Hudson waterfront, including several major banks with Jersey City technology offices, also file H-1B petitions regularly for software design engineering roles. Consulting firms with New Jersey delivery centers are another consistent source of sponsorship.
Which visa types are most common for software design engineer roles in New Jersey?
The H-1B is the most common visa for software design engineers in New Jersey, given the role's classification as a specialty occupation requiring a relevant bachelor's degree or higher. Candidates already holding L-1B intracompany transferee status through multinational employers with New Jersey offices represent another pathway. Canadians and Mexicans may also qualify under the TN visa category for computer engineering roles.
Which cities in New Jersey have the most software design engineer sponsorship jobs?
Jersey City and Newark generate the highest concentration of software design engineer sponsorship activity, largely due to proximity to New York City and the presence of financial technology and consulting firm offices. Princeton attracts engineering talent through pharmaceutical and research-adjacent technology roles. Parsippany and Bridgewater also have active employer bases in enterprise software and life sciences technology.
How to find software design engineer visa sponsorship jobs in New Jersey?
Migrate Mate filters job listings specifically by visa sponsorship availability, so you can browse software design engineer roles in New Jersey without manually screening hundreds of postings. The platform surfaces employers actively filing H-1B and other work visa petitions for engineering positions across Jersey City, Newark, Princeton, and surrounding areas, which significantly narrows the search for international candidates.
Are there state-specific factors that affect software design engineer sponsorship hiring in New Jersey?
New Jersey's concentration of pharmaceutical, financial services, and enterprise technology employers creates strong demand for software design engineers with domain-specific experience. The state also benefits from a university pipeline through Rutgers University and the New Jersey Institute of Technology, both producing a high volume of engineering graduates. Employers in regulated industries like life sciences tend to have established immigration counsel and more structured sponsorship processes.
What is the prevailing wage for sponsored software design engineer jobs in New Jersey?
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.