Quality Assurance Engineer Visa Sponsorship Jobs in New Hampshire
Quality assurance engineer visa sponsorship jobs in New Hampshire are concentrated around the Manchester and Nashua corridors, where defense contractors like BAE Systems and medical device manufacturers maintain significant engineering operations. The state's proximity to Boston's tech ecosystem also draws software-focused QA roles, particularly in automated testing and embedded systems.
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Get Access To All JobsDate: Jul 27, 2026
Location:
Merrimack, NH, US
Company: Atrium Medical Corporation
Remote Work: 1-2 days at home (site based)
Salary Range: $90K to 110K with 8% STIP
With a passion for life
Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers.
Are you looking for an inspiring career? You just found it.
Job Overview
Provide Quality Assurance level support and oversight to Corrective and Preventive Action (CAPA) activities to ensure effective and timely CAPAs. Support other activities within the Quality Compliance department. Drive continuous improvement activities.
Job Responsibilities and Essential Duties
CAPA
As a CAPA Coordinator, lead CAPA Request and CAPA teams throughout the CAPA process for successful completion of CAPA activities.
- Provide project management support to ensure CAPA activities and timelines are agreed upon, communicated, managed, and met.
- Review CAPA Request and CAPA documentation to ensure CAPA activities are performed and documented per procedures and regulations.
- Drive problem definition and scoping of CAPAs to assure CAPAs will appropriately address underlying issues.
- Facilitate and lead failure investigations and root cause analyses.
- Develop effectiveness check criteria.
- Perform CAPA verification of implementation and verification of effectiveness activities.
- Process CAPA documentation within the electronic systems.
- Communicate reminders of actions needed to personnel at all levels within the organization.
- Provide training on the CAPA process as needed.
- Schedule review of CAPA documentation with the CAPA Review Board.
- Serve as facilitator of the CAPA Review Board meetings and take meeting minutes.
- Prepare documentation for trending & metrics using Microsoft Office (Excel, PowerPoint).
Quality Compliance
Execute tasks and projects that impact the Quality Management System (QMS) as required.
- Perform analysis on a new or revised standard and execute deliverables to support continuous compliance to applicable current standards and regulations.
- Perform Verification of Implementation (VOI) and Effectivity (VOE) of corrective actions.
- Improve and maintain the QMS in line with ISO 13485, Medical Device Regulation (EU-MDR), MDSAP International Regulations (Australia, Brazil, Canada, Japan, USA) and regulatory requirements applicable to the Quality Management System Regulation (QMSR).
Other
Assist in meeting departmental goals and special projects as assigned.
- Support external audits in various roles as assigned: scribe, backroom technical support and file preparation.
- Prepare documentation needed to fulfill requests from customers (internal and external).
- Perform other duties, as assigned.
Minimum Requirements
Bachelor’s degree in engineering discipline or scientific discipline (e.g. Chemistry, Biology, Physics) or equivalent experience.
- 2+ years’ quality experience or equivalent, working in medical device industry or other highly regulated industry.
- Experience performing root cause investigations.
Required Knowledge, Skills and Abilities
- High level of attention to detail and accuracy.
- Strong problem-solving skills and experience using root cause analysis techniques.
- Strong oral and written communication skills. Ability to prepare well written reports.
- Ability to interact and communicate with all levels of personnel from various functions.
- Ability to manage projects involving cross-functional membership.
- Ability to prioritize and manage key deliverables and work on multiple tasks/projects.
- Knowledge of Quality Systems, ISO 13485 and FDA requirements.
- Knowledge of CAPA, NCR, supplier controls, process controls, design controls, verification and validation, and risk management systems.
- Strong computer skills, including MS Office applications (Word/Excel/Power Point/Outlook/Teams).
- Knowledge of statistics. Ability to perform data mining, analyze data and interpret results.
Supervision/Management Of Others:
Not Applicable
Internal and External Contacts/Relationships
- Interaction with all levels of personnel from various functions
- Interaction with cross-functional teams/departments
- Interaction with representatives from regulatory agencies and bodies
Environmental/Safety/Physical Work Conditions
- Ensures environmental consciousness and safe practices are exhibited in decisions.
- Use of computer and telephone equipment and other related office accessories/devices to complete assignments.
- Hybrid office environment
- May work extended hours during peak business cycles.
- Occasional work in controlled environment
Annual Salary of $90K to 110K with 8% STIP
LI-YA2 #LI-Hybrid
About us
With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.
Benefits at Getinge:
At Getinge, we offer a comprehensive benefits package, which includes:
- Health, Dental, and Vision insurance benefits
- 401k plan with company match
- Paid Time Off
- Wellness initiative & Health Assistance Resources
- Life Insurance
- Short and Long Term Disability Benefits
- Health and Dependent Care Flexible Spending Accounts
- Commuter Benefits
- Parental and Caregiver Leave
- Tuition Reimbursement
Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.
Date: Jul 27, 2026
Location:
Merrimack, NH, US
Company: Atrium Medical Corporation
Remote Work: 1-2 days at home (site based)
Salary Range: $90K to 110K with 8% STIP
With a passion for life
Join our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers – and to save more lives, we need team players, forward thinkers, and game changers.
Are you looking for an inspiring career? You just found it.
Job Overview
Provide Quality Assurance level support and oversight to Corrective and Preventive Action (CAPA) activities to ensure effective and timely CAPAs. Support other activities within the Quality Compliance department. Drive continuous improvement activities.
Job Responsibilities and Essential Duties
CAPA
As a CAPA Coordinator, lead CAPA Request and CAPA teams throughout the CAPA process for successful completion of CAPA activities.
- Provide project management support to ensure CAPA activities and timelines are agreed upon, communicated, managed, and met.
- Review CAPA Request and CAPA documentation to ensure CAPA activities are performed and documented per procedures and regulations.
- Drive problem definition and scoping of CAPAs to assure CAPAs will appropriately address underlying issues.
- Facilitate and lead failure investigations and root cause analyses.
- Develop effectiveness check criteria.
- Perform CAPA verification of implementation and verification of effectiveness activities.
- Process CAPA documentation within the electronic systems.
- Communicate reminders of actions needed to personnel at all levels within the organization.
- Provide training on the CAPA process as needed.
- Schedule review of CAPA documentation with the CAPA Review Board.
- Serve as facilitator of the CAPA Review Board meetings and take meeting minutes.
- Prepare documentation for trending & metrics using Microsoft Office (Excel, PowerPoint).
Quality Compliance
Execute tasks and projects that impact the Quality Management System (QMS) as required.
- Perform analysis on a new or revised standard and execute deliverables to support continuous compliance to applicable current standards and regulations.
- Perform Verification of Implementation (VOI) and Effectivity (VOE) of corrective actions.
- Improve and maintain the QMS in line with ISO 13485, Medical Device Regulation (EU-MDR), MDSAP International Regulations (Australia, Brazil, Canada, Japan, USA) and regulatory requirements applicable to the Quality Management System Regulation (QMSR).
Other
Assist in meeting departmental goals and special projects as assigned.
- Support external audits in various roles as assigned: scribe, backroom technical support and file preparation.
- Prepare documentation needed to fulfill requests from customers (internal and external).
- Perform other duties, as assigned.
Minimum Requirements
Bachelor’s degree in engineering discipline or scientific discipline (e.g. Chemistry, Biology, Physics) or equivalent experience.
- 2+ years’ quality experience or equivalent, working in medical device industry or other highly regulated industry.
- Experience performing root cause investigations.
Required Knowledge, Skills and Abilities
- High level of attention to detail and accuracy.
- Strong problem-solving skills and experience using root cause analysis techniques.
- Strong oral and written communication skills. Ability to prepare well written reports.
- Ability to interact and communicate with all levels of personnel from various functions.
- Ability to manage projects involving cross-functional membership.
- Ability to prioritize and manage key deliverables and work on multiple tasks/projects.
- Knowledge of Quality Systems, ISO 13485 and FDA requirements.
- Knowledge of CAPA, NCR, supplier controls, process controls, design controls, verification and validation, and risk management systems.
- Strong computer skills, including MS Office applications (Word/Excel/Power Point/Outlook/Teams).
- Knowledge of statistics. Ability to perform data mining, analyze data and interpret results.
Supervision/Management Of Others:
Not Applicable
Internal and External Contacts/Relationships
- Interaction with all levels of personnel from various functions
- Interaction with cross-functional teams/departments
- Interaction with representatives from regulatory agencies and bodies
Environmental/Safety/Physical Work Conditions
- Ensures environmental consciousness and safe practices are exhibited in decisions.
- Use of computer and telephone equipment and other related office accessories/devices to complete assignments.
- Hybrid office environment
- May work extended hours during peak business cycles.
- Occasional work in controlled environment
Annual Salary of $90K to 110K with 8% STIP
LI-YA2 #LI-Hybrid
About us
With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.
Benefits at Getinge:
At Getinge, we offer a comprehensive benefits package, which includes:
- Health, Dental, and Vision insurance benefits
- 401k plan with company match
- Paid Time Off
- Wellness initiative & Health Assistance Resources
- Life Insurance
- Short and Long Term Disability Benefits
- Health and Dependent Care Flexible Spending Accounts
- Commuter Benefits
- Parental and Caregiver Leave
- Tuition Reimbursement
Getinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. Reasonable accommodations are available upon request for candidates taking part in all aspects of the selection process.
Quality Assurance Engineer Job Roles in New Hampshire
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Search Quality Assurance Engineer Jobs in New HampshireQuality Assurance Engineer Jobs in New Hampshire: Frequently Asked Questions
Which companies sponsor visas for quality assurance engineers in New Hampshire?
Defense and aerospace contractors are among the most active sponsors for quality assurance engineers in New Hampshire. BAE Systems in Nashua has a history of H-1B visa filings for engineering roles, as do medical device and semiconductor firms operating in the Manchester area. Smaller software companies along the Route 3 corridor also sponsor QA engineers, particularly for roles requiring expertise in automated testing frameworks.
Which visa types are most common for quality assurance engineer roles in New Hampshire?
The H-1B is the most common visa category for quality assurance engineers in New Hampshire, as QA engineer roles typically qualify as specialty occupations requiring a bachelor's degree in computer science, engineering, or a related field. Candidates from Canada or Mexico may be eligible for TN visa status under the USMCA, which covers engineers without requiring a petition or lottery. Australians with relevant qualifications may consider the E-3 visa.
Which cities in New Hampshire have the most quality assurance engineer sponsorship jobs?
Nashua and Manchester account for the majority of quality assurance engineer sponsorship activity in New Hampshire. Nashua's concentration of defense and electronics firms, including BAE Systems and several semiconductor companies, drives consistent demand for QA engineers. Manchester, as the state's largest city, hosts a broader mix of software and healthcare technology employers. Bedford and Merrimack also see QA hiring from employers with campuses in southern New Hampshire.
How to find quality assurance engineer visa sponsorship jobs in New Hampshire?
Migrate Mate is built specifically for international job seekers and filters quality assurance engineer roles in New Hampshire by visa sponsorship availability, so you're not sorting through listings from employers who won't sponsor. The platform covers H-1B, E-3 visa, TN, and other work visa categories. Focusing your search on southern New Hampshire cities like Nashua and Manchester will surface the highest concentration of QA engineering opportunities with sponsorship.
Are there state-specific factors that affect visa sponsorship for QA engineers in New Hampshire?
New Hampshire has no state income tax, which can make it an attractive location for employers competing for engineering talent, though this does not directly affect sponsorship eligibility. A notable consideration for QA roles in defense-adjacent companies is security clearance requirements: some positions require U.S. citizenship or permanent residency, which excludes candidates on nonimmigrant visas. Confirming clearance requirements before applying is important for roles at firms like BAE Systems or Raytheon.
What is the prevailing wage for sponsored quality assurance 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.