Systems Engineer Visa Sponsorship Jobs in New Hampshire
Systems engineer visa sponsorship jobs in New Hampshire are concentrated around the Manchester-Nashua corridor and the seacoast region, with employers like BAE Systems, Raytheon, and Liberty Mutual hiring in defense, aerospace, and technology. The state's proximity to Boston expands the opportunity pool without the cost of living penalty.
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Get Access To All JobsINTRODUCTION
DEKA is hiring a Senior Quality Systems Engineer to own the system-level work that keeps our QMS audit-ready. As a Senior Quality Systems Engineer, you'll be working closely with the QA & Compliance Manager and partnering across Engineering, Operations, Regulatory, and Manufacturing to strengthen and mature the DEKA QMS.
ROLE AND RESPONSIBILITIES
As a Senior Quality Systems Engineer, you will contribute in the following areas:
- Develop and apply a deep working knowledge of DEKA's QMS to identify, propose, and implement system improvements to ensure ongoing compliance with FDA 21 CFR Part 820, FDA QMSR, and ISO 13485.
- Apply risk-based decision-making to:
- Ensure the quality system is fit for purpose, and drive QMS improvements and changes through to implementation.
- Partner with project teams to implement QMS requirements at the project level, providing practical solutions and alternative compliance paths that meet regulatory expectations without stalling project execution.
- Lead cross-functional CAPA review meetings, guiding teams through systemic issue identification and alignment on remediation strategies. In some cases, this role will also own CAPAs and drive root cause investigations.
- Monitor CAPA trends and performance metrics to identify recurring issues and drive continuous improvement across the QMS.
- Develop and revise system-level SOPs and associated change controls to align with regulatory requirements and maintain QMS compliance.
- Develop training, and mentor junior team members.
- Review quality plans, documents, and records, ensuring accuracy, completeness, and adherence to applicable requirements.
- Plan and conduct audits (e.g., Internal, FDA, ISO, customer audits).
- Prepare inputs and supporting analysis for Management Review.
BASIC QUALIFICATIONS
As a senior contributor to our team, you will demonstrate the following skills:
- Strong technical writing skills: you produce precise, audit-ready documentation and translate complex concepts clearly for diverse audiences.
- A natural curiosity and ability to quickly grasp technical systems, workflows, and requirements.
- Clear, confident communication: you know how to explain problems and solutions across a range of technical backgrounds and hold a position with engineering, operations, and leadership.
- Strong project ownership and follow-through and keep things moving without close oversight.
- A proactive problem-solver mindset: you ask the right questions, challenge assumptions, and help teams find workable solutions.
- Collaborative energy: you contribute, share ideas, and maintain a constructive, can-do attitude.
- Precision and attention to detail: your work is thorough, consistent, and traceable.
- Reliability: you take ownership, meet deadlines, and follow through.
REQUIRED TRAINING / KNOWLEDGE
- BS in Engineering, Life Sciences, or related field
- 5+ years in a quality systems role in a regulated industry, medical devices preferred
- Demonstrated experience authoring and/or updating system-level QMS procedures
- Prior experience leading internal audits and supporting external audits (FDA, notified body, customer)
- Prior experience owning, implementing, and verifying complex CAPAs
- Proficiency in FDA QMSR (21 CFR Part 820) regulations, and ISO 13485 and ISO 14971 standards
- Experience with eQMS platforms
- Proficiency with Microsoft Office and Visio
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 & 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 is hiring a Senior Quality Systems Engineer to own the system-level work that keeps our QMS audit-ready. As a Senior Quality Systems Engineer, you'll be working closely with the QA & Compliance Manager and partnering across Engineering, Operations, Regulatory, and Manufacturing to strengthen and mature the DEKA QMS.
ROLE AND RESPONSIBILITIES
As a Senior Quality Systems Engineer, you will contribute in the following areas:
- Develop and apply a deep working knowledge of DEKA's QMS to identify, propose, and implement system improvements to ensure ongoing compliance with FDA 21 CFR Part 820, FDA QMSR, and ISO 13485.
- Apply risk-based decision-making to:
- Ensure the quality system is fit for purpose, and drive QMS improvements and changes through to implementation.
- Partner with project teams to implement QMS requirements at the project level, providing practical solutions and alternative compliance paths that meet regulatory expectations without stalling project execution.
- Lead cross-functional CAPA review meetings, guiding teams through systemic issue identification and alignment on remediation strategies. In some cases, this role will also own CAPAs and drive root cause investigations.
- Monitor CAPA trends and performance metrics to identify recurring issues and drive continuous improvement across the QMS.
- Develop and revise system-level SOPs and associated change controls to align with regulatory requirements and maintain QMS compliance.
- Develop training, and mentor junior team members.
- Review quality plans, documents, and records, ensuring accuracy, completeness, and adherence to applicable requirements.
- Plan and conduct audits (e.g., Internal, FDA, ISO, customer audits).
- Prepare inputs and supporting analysis for Management Review.
BASIC QUALIFICATIONS
As a senior contributor to our team, you will demonstrate the following skills:
- Strong technical writing skills: you produce precise, audit-ready documentation and translate complex concepts clearly for diverse audiences.
- A natural curiosity and ability to quickly grasp technical systems, workflows, and requirements.
- Clear, confident communication: you know how to explain problems and solutions across a range of technical backgrounds and hold a position with engineering, operations, and leadership.
- Strong project ownership and follow-through and keep things moving without close oversight.
- A proactive problem-solver mindset: you ask the right questions, challenge assumptions, and help teams find workable solutions.
- Collaborative energy: you contribute, share ideas, and maintain a constructive, can-do attitude.
- Precision and attention to detail: your work is thorough, consistent, and traceable.
- Reliability: you take ownership, meet deadlines, and follow through.
REQUIRED TRAINING / KNOWLEDGE
- BS in Engineering, Life Sciences, or related field
- 5+ years in a quality systems role in a regulated industry, medical devices preferred
- Demonstrated experience authoring and/or updating system-level QMS procedures
- Prior experience leading internal audits and supporting external audits (FDA, notified body, customer)
- Prior experience owning, implementing, and verifying complex CAPAs
- Proficiency in FDA QMSR (21 CFR Part 820) regulations, and ISO 13485 and ISO 14971 standards
- Experience with eQMS platforms
- Proficiency with Microsoft Office and Visio
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 & 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.
Systems Engineer Job Roles in New Hampshire
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Search Systems Engineer Jobs in New HampshireSystems Engineer Jobs in New Hampshire: Frequently Asked Questions
Which companies sponsor visas for systems engineers in New Hampshire?
BAE Systems and Raytheon are among the most active sponsors for systems engineers in New Hampshire, particularly for defense and aerospace roles in Nashua and Manchester. Liberty Mutual's technology operations in Dover and smaller defense contractors throughout the state also file H-1B visa petitions for systems engineering positions. Sponsorship activity tends to follow Department of Defense contract cycles in this state.
Which visa types are most common for systems engineer roles in New Hampshire?
The H-1B is the most common visa category for systems engineers in New Hampshire, as the role consistently qualifies as a specialty occupation requiring at least a bachelor's degree in systems engineering, computer science, or a related field. Candidates with Canadian or Mexican citizenship may qualify for TN visa status under the engineer category. Applicants with extraordinary ability credentials may also explore the O-1A.
Which cities in New Hampshire have the most systems engineer sponsorship jobs?
Nashua and Manchester account for the largest share of systems engineer sponsorship activity in New Hampshire. Nashua's concentration of defense contractors, including BAE Systems and several aerospace suppliers, makes it the primary hub. Manchester follows as the state's largest city with a broader technology employer base. The seacoast area around Portsmouth also sees hiring activity tied to defense and government contracting work.
How to find systems engineer visa sponsorship jobs in New Hampshire?
Migrate Mate filters job listings specifically for roles that include visa sponsorship, making it straightforward to search for systems engineer positions in New Hampshire without sifting through employers who won't sponsor. You can narrow results by location and role to focus on Nashua, Manchester, or Portsmouth. Migrate Mate also surfaces employers with a track record of H-1B filings in the state, which is useful context when evaluating opportunities.
Are there any state-specific considerations for systems engineers seeking sponsorship in New Hampshire?
New Hampshire's systems engineering market is heavily influenced by Department of Defense contracts, which means many roles require or eventually require security clearances. Non-U.S. citizens on work visas are generally not eligible for security clearances, which can limit access to certain positions even at companies that otherwise sponsor visas. Candidates should confirm whether a posted role has a clearance requirement before pursuing it. University of New Hampshire and Southern New Hampshire University contribute some local talent, but most employers also recruit nationally.
What is the prevailing wage for sponsored systems 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.