Product Engineer Visa Sponsorship Jobs in New Hampshire
Product engineer roles in New Hampshire are concentrated around the Manchester and Nashua corridors, where companies like BAE Systems, Benchmark Electronics, and Segra International maintain engineering operations. The state's proximity to Boston attracts mid-size tech and defense firms that regularly hire internationally, making it a realistic market for candidates seeking visa sponsorship.
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Get Access To All JobsINTRODUCTION
DEKA R&D, on behalf of Millyard Advanced Medical Products, is looking for a Product Complaints Engineer to work in a dynamic Medical Device Research and Development environment. The position reports to the Product Complaints Manager. This is a high visibility role with a significant direct impact in the Quality Management System.
HOW YOU WILL MAKE AN IMPACT:
- Responsible for reviewing complaints related to potential medical device issues.
- Perform product complaint evaluations with minimal direction, utilizing experience and product knowledge.
- Ensure that complaint documentation follows Good Documentation Practices; meets QMS requirements; and complies with U.S. Food and Drug Administration (FDA) regulations / other regulatory requirements.
- Identify and make sound decisions regarding medical device reporting to regulatory agencies.
- Interface with Third Party Manufacturers, health care professionals, internal customers, and regulatory agencies.
- Participate in audits and CAPA investigations as they relate to complaint handling.
- Work with the forensic investigation team to align product investigations related to complaints.
- Generate reports to identify areas of process improvement.
- Develop product training aids.
- Contribute independently while also collaborating with other team members and departments needing product complaint information.
- Maintain positive and cooperative communication with co-workers, customers, contractors, and vendors.
- Serve as a subject matter expert on complaint handling.
- Perform other related duties as assigned under management supervision.
BASIC QUALIFICATIONS
- Bachelor's degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Quality Engineering, or a related technical discipline required.
- Minimum of 3-5 years of experience in a regulated medical device, pharmaceutical, or life sciences environment, with direct responsibility for complaint investigations, product quality investigations, product analysis, and complaint closure activities.
- Demonstrated experience conducting complaint investigations, determining root cause, documenting investigation results, and independently driving records to closure in compliance with established timelines.
- Working knowledge of FDA Quality System Regulations, Medical Device Reporting requirements, and applicable standards, including 21 CFR Parts 803 and 820; experience with ISO 13485 is preferred.
- Experience evaluating product complaints for reportability and supporting regulatory submissions is preferred.
- Experience using electronic quality management systems (eQMS), complaint handling systems, and platforms such as Salesforce is preferred.
- Strong technical troubleshooting, analytical, and problem-solving skills with the ability to assess complex product performance issues and identify potential failure modes.
- Exceptional time management skills with the ability to manage a high-volume complaint workload while meeting regulatory and internal closure targets.
- Excellent technical writing skills with demonstrated ability to prepare clear, concise, and compliant investigation reports.
- Strong written and verbal communication skills with the ability to effectively interact with Quality, Regulatory, Engineering, Manufacturing, Clinical, and Customer Support teams.
- Highly organized, detail-oriented, and self-motivated with the ability to work independently and make sound decisions based on available evidence.
- Ability to thrive in a fast-paced, changing environment while maintaining compliance with regulations, procedures, and quality system requirements.
ABOUT MILLYARD ADVANCED MEDICAL PRODUCTS
Located in the heart of the Regen Valley in Manchester, NH, our company aims to positively influence the healthcare landscape.
ESTABLISHED 2019
SELECTED PARTNERS
- Contract Designer: DEKA Research & Development
- Contract Manufacturer: Merrimack Manufacturing
ABOUT DEKA
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
INTRODUCTION
DEKA R&D, on behalf of Millyard Advanced Medical Products, is looking for a Product Complaints Engineer to work in a dynamic Medical Device Research and Development environment. The position reports to the Product Complaints Manager. This is a high visibility role with a significant direct impact in the Quality Management System.
HOW YOU WILL MAKE AN IMPACT:
- Responsible for reviewing complaints related to potential medical device issues.
- Perform product complaint evaluations with minimal direction, utilizing experience and product knowledge.
- Ensure that complaint documentation follows Good Documentation Practices; meets QMS requirements; and complies with U.S. Food and Drug Administration (FDA) regulations / other regulatory requirements.
- Identify and make sound decisions regarding medical device reporting to regulatory agencies.
- Interface with Third Party Manufacturers, health care professionals, internal customers, and regulatory agencies.
- Participate in audits and CAPA investigations as they relate to complaint handling.
- Work with the forensic investigation team to align product investigations related to complaints.
- Generate reports to identify areas of process improvement.
- Develop product training aids.
- Contribute independently while also collaborating with other team members and departments needing product complaint information.
- Maintain positive and cooperative communication with co-workers, customers, contractors, and vendors.
- Serve as a subject matter expert on complaint handling.
- Perform other related duties as assigned under management supervision.
BASIC QUALIFICATIONS
- Bachelor's degree in Biomedical Engineering, Mechanical Engineering, Electrical Engineering, Quality Engineering, or a related technical discipline required.
- Minimum of 3-5 years of experience in a regulated medical device, pharmaceutical, or life sciences environment, with direct responsibility for complaint investigations, product quality investigations, product analysis, and complaint closure activities.
- Demonstrated experience conducting complaint investigations, determining root cause, documenting investigation results, and independently driving records to closure in compliance with established timelines.
- Working knowledge of FDA Quality System Regulations, Medical Device Reporting requirements, and applicable standards, including 21 CFR Parts 803 and 820; experience with ISO 13485 is preferred.
- Experience evaluating product complaints for reportability and supporting regulatory submissions is preferred.
- Experience using electronic quality management systems (eQMS), complaint handling systems, and platforms such as Salesforce is preferred.
- Strong technical troubleshooting, analytical, and problem-solving skills with the ability to assess complex product performance issues and identify potential failure modes.
- Exceptional time management skills with the ability to manage a high-volume complaint workload while meeting regulatory and internal closure targets.
- Excellent technical writing skills with demonstrated ability to prepare clear, concise, and compliant investigation reports.
- Strong written and verbal communication skills with the ability to effectively interact with Quality, Regulatory, Engineering, Manufacturing, Clinical, and Customer Support teams.
- Highly organized, detail-oriented, and self-motivated with the ability to work independently and make sound decisions based on available evidence.
- Ability to thrive in a fast-paced, changing environment while maintaining compliance with regulations, procedures, and quality system requirements.
ABOUT MILLYARD ADVANCED MEDICAL PRODUCTS
Located in the heart of the Regen Valley in Manchester, NH, our company aims to positively influence the healthcare landscape.
ESTABLISHED 2019
SELECTED PARTNERS
- Contract Designer: DEKA Research & Development
- Contract Manufacturer: Merrimack Manufacturing
ABOUT DEKA
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research and Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
Product Engineer Job Roles in New Hampshire
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Search Product Engineer Jobs in New HampshireProduct Engineer Jobs in New Hampshire: Frequently Asked Questions
Which companies sponsor visas for product engineers in New Hampshire?
BAE Systems, Benchmark Electronics, and Amphenol are among the larger employers in New Hampshire with documented H-1B visa sponsorship histories for engineering roles. Defense contractors and advanced manufacturing firms in the Manchester-Nashua corridor tend to sponsor more consistently than smaller companies, given their federal contracting relationships and established HR infrastructure for international hiring.
Which visa types are most common for product engineer roles in New Hampshire?
The H-1B is the most common visa category for product engineers in New Hampshire, as the role typically qualifies as a specialty occupation requiring at least a bachelor's degree in engineering or a related field. Candidates from Canada or Mexico may also pursue TN visa status under the USMCA, and those with extraordinary ability may consider the O-1A, though that category has a significantly higher evidentiary bar.
Which cities in New Hampshire have the most product engineer sponsorship jobs?
Manchester and Nashua account for the largest share of product engineer sponsorship activity in New Hampshire. Nashua in particular hosts a cluster of electronics and defense manufacturers along the Massachusetts border. Portsmouth sees some activity driven by naval and maritime industries, while Concord, as the state capital, has smaller but steady engineering demand across government-adjacent contractors.
How to find product engineer visa sponsorship jobs in New Hampshire?
Migrate Mate filters product engineer roles specifically by visa sponsorship availability, so you can browse New Hampshire opportunities without sifting through listings where sponsorship isn't offered. The platform is built for international candidates, which means job listings are already screened for employer willingness to sponsor. Searching by state and role on Migrate Mate is the most direct way to find current openings in New Hampshire.
Are there any state-specific considerations for product engineers seeking sponsorship in New Hampshire?
New Hampshire has no state income tax, which affects prevailing wage comparisons employers must document for H-1B Labor Condition Applications. The Department of Labor requires employers to pay at least the prevailing wage for the specific role and location, and New Hampshire wage benchmarks reflect regional market rates rather than Boston-level figures. The state's defense and advanced manufacturing sectors also mean some roles carry security clearance requirements, which can complicate sponsorship for non-citizens.
What is the prevailing wage for sponsored product engineer jobs in New Hampshire?
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.