H-1B Visa Software Quality Assurance Manager Jobs
H-1B visa jobs for Software Quality Assurance Managers are sponsored by employers who need degree-level expertise in software testing methodologies, QA frameworks, and engineering processes. This role typically qualifies as a specialty occupation under H-1B rules, making it a strong fit for professionals with a bachelor's degree in computer science, software engineering, or a related field.
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Get Access To All JobsLocation: Remote, Texas, United States of America
Category: Quality Assurance & Regulatory Affairs
Job ID: JR-14791
widget: Full time
Posted Date: November 5th 2026
undefined: Regular
Description
As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow—because at LivaNova, we don’t just treat conditions — we aspire to alter the course of lives.
Senior Manager, Software Quality Assurance
Pay Transparency: A reasonable estimate of the annual base salary for this position is $150,000 - $175,000 plus discretionary annual bonus. Pay ranges may vary by location.
As our Senior Manager, Software Quality Assurance, you will lead the software quality function while applying hands-on software development knowledge to ensure product software, firmware, and digital health platform services are designed, developed, verified, validated, and released in compliance with applicable quality system procedures. You will provide strategic and operational leadership to software quality engineers, drive continuous improvement in software quality processes, and ensure robust risk management throughout the software lifecycle.
You and your team will partner with key stakeholders to provide cross-functional support, contribute to design history file content, and, where applicable to your areas of expertise, lead post-market product investigations, CAPAs, and provide audit support. This is a full-time, remote position and may include up to 25% travel.
This is an opportunity to directly impact product quality and improve user experience. LivaNova is a growing, cutting-edge, medical device company specializing in neuromodulation products that enrich patients' lives.
- Team Leadership and Development: Recruit, mentor, coach, and develop software quality engineers. Lead the software and firmware quality function for product software and cloud infrastructure, including the digital health platform.
- Design Control Oversight: Ensure the completeness and sufficiency of design requirements, architecture specifications, detailed design specifications, code review evidence, verification and validation evidence, risk management files, and traceability.
- Change Control Governance: Chair or oversee software change control boards and defect management processes. Communicate V&V results to management, including summaries of outcomes and known software anomalies.
- Cross-Functional Partnership: Build strategic alignment with partner organizations, including R&D, Regulatory, Operations, Security, Marketing, and Clinical.
- Risk Management Stewardship: Maintain working knowledge of program hazard analyses, FMEAs, security risk assessments, risk management reports, and post-market lifecycle risk documentation.
- Technical Decision-Making: Approve complex investigations, technical assessments, code-related quality conclusions, and quality-critical decisions. Manage the team to ensure on-time delivery of investigations, CAPAs, and audit responses.
- Quality Management System Ownership: Maintain and improve software development, test, and change management procedures, as well as best practices for digital health platform management.
- Manufacturing Software Validation: Demonstrate a deep understanding of validation requirements and processes. Ensure team members support compliant validation of manufacturing and test system software as part of new product development programs.
- Audit and Inspection Readiness: Serve as a senior SME during internal audits and external regulatory inspections. Ensure the team delivers efficient, complete design history files with the elements necessary to demonstrate compliance.
- Stakeholder Communication: Communicate software quality status, risks, and mitigation strategies to senior leadership. Organize and support cross-functional efforts in the event of field actions.
- Continuous Improvement: Lead initiatives that strengthen software quality processes, tools, and metrics.
Your Background and Experience
The following represent the minimum qualifications:
- Engineering Degree — BS in Computer Engineering, Computer Science, Electrical Engineering, or related field. Advanced Degree Preferred — MS or higher in engineering or a software-related discipline preferred.
- 8+ years of medical device experience and 3+ years of prior team management experience.
- Medical Device Software and Quality Expertise: Deep knowledge of software development principles, ISO 13485, IEC 62304, FDA QMSR, ISO 14971, and cybersecurity requirements.
- Demonstrated experience developing software or firmware in the medical device industry, combined with software quality leadership experience and demonstrated proficiency with IEC 62304 requirements. Candidates must possess technical capability in software development, preferably C or C#, including the ability to assess code reviews, software defects, verification results, and CAPA conclusions.
- Strategic Quality Planning; Risk Management Leadership; Audit Expertise; Ability to lead strategy and provide technical direction for complex software investigations, CAPAs, quality decisions, and development-related risk assessments.
What We Can Offer You
At LivaNova, you'll help change the trajectory of lives for a new day while working alongside passionate teams dedicated to delivering impactful innovation for patients worldwide.
We offer:
- A role in an innovative medical technology environment that supports professional growth and development.
- Opportunities to collaborate with international partners and cross-functional teams to bring life-changing solutions to patients.
- A culture grounded in Empowered Accountability, Curious Mindset, Constructive Collaboration, and Thoughtful Humility.
- Competitive compensation and an inspiring place to work.
If you're inspired by purpose-driven work, meaningful innovation, and the opportunity to bring New Life in Action every day, we encourage you to apply. We look forward to hearing from you.
Valuing different backgrounds:
LivaNova values equality and diversity. We are committed to ensuring that our recruitment process is fair, transparent and free from unlawful discrimination. Our selection process is driven by the key demands/requirements for the role rather than bias or discrimination on the basis of a candidate’s sex, gender identity, age, marital status, veteran status, non-job-related disability/handicap or medical condition, family status, sexual orientation, religion, color, ethnicity, race or any other legally protected classification.
Notice to third party agencies:
Please note that we do not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Recruitment Services Agreement, we will not consider, or agree to, payment of any referral compensation or recruiter fee. In the event that a recruiter or agency submits a resume or candidate without a previously signed agreement, we explicitly reserve the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency.
Beware of Job Scams:
Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons posing as LivaNova recruiters or employees. The scammers may attempt to solicit confidential, personal information, such as a social security number, or your financial information. LivaNova will never ask for fees prior/during/after the application process, nor will we ask for banking details or personal financial information in return for the assurance of employment. If you are concerned that an offer of employment might be a scam or that the recruiter is not legitimate, please verify by searching for “See Open Jobs” on https://www.livanova.com/en-us/careers, and check that all recruitment emails come from an @livanova.com email address.
Location: Remote, Texas, United States of America
Category: Quality Assurance & Regulatory Affairs
Job ID: JR-14791
widget: Full time
Posted Date: November 5th 2026
undefined: Regular
Description
As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow—because at LivaNova, we don’t just treat conditions — we aspire to alter the course of lives.
Senior Manager, Software Quality Assurance
Pay Transparency: A reasonable estimate of the annual base salary for this position is $150,000 - $175,000 plus discretionary annual bonus. Pay ranges may vary by location.
As our Senior Manager, Software Quality Assurance, you will lead the software quality function while applying hands-on software development knowledge to ensure product software, firmware, and digital health platform services are designed, developed, verified, validated, and released in compliance with applicable quality system procedures. You will provide strategic and operational leadership to software quality engineers, drive continuous improvement in software quality processes, and ensure robust risk management throughout the software lifecycle.
You and your team will partner with key stakeholders to provide cross-functional support, contribute to design history file content, and, where applicable to your areas of expertise, lead post-market product investigations, CAPAs, and provide audit support. This is a full-time, remote position and may include up to 25% travel.
This is an opportunity to directly impact product quality and improve user experience. LivaNova is a growing, cutting-edge, medical device company specializing in neuromodulation products that enrich patients' lives.
- Team Leadership and Development: Recruit, mentor, coach, and develop software quality engineers. Lead the software and firmware quality function for product software and cloud infrastructure, including the digital health platform.
- Design Control Oversight: Ensure the completeness and sufficiency of design requirements, architecture specifications, detailed design specifications, code review evidence, verification and validation evidence, risk management files, and traceability.
- Change Control Governance: Chair or oversee software change control boards and defect management processes. Communicate V&V results to management, including summaries of outcomes and known software anomalies.
- Cross-Functional Partnership: Build strategic alignment with partner organizations, including R&D, Regulatory, Operations, Security, Marketing, and Clinical.
- Risk Management Stewardship: Maintain working knowledge of program hazard analyses, FMEAs, security risk assessments, risk management reports, and post-market lifecycle risk documentation.
- Technical Decision-Making: Approve complex investigations, technical assessments, code-related quality conclusions, and quality-critical decisions. Manage the team to ensure on-time delivery of investigations, CAPAs, and audit responses.
- Quality Management System Ownership: Maintain and improve software development, test, and change management procedures, as well as best practices for digital health platform management.
- Manufacturing Software Validation: Demonstrate a deep understanding of validation requirements and processes. Ensure team members support compliant validation of manufacturing and test system software as part of new product development programs.
- Audit and Inspection Readiness: Serve as a senior SME during internal audits and external regulatory inspections. Ensure the team delivers efficient, complete design history files with the elements necessary to demonstrate compliance.
- Stakeholder Communication: Communicate software quality status, risks, and mitigation strategies to senior leadership. Organize and support cross-functional efforts in the event of field actions.
- Continuous Improvement: Lead initiatives that strengthen software quality processes, tools, and metrics.
Your Background and Experience
The following represent the minimum qualifications:
- Engineering Degree — BS in Computer Engineering, Computer Science, Electrical Engineering, or related field. Advanced Degree Preferred — MS or higher in engineering or a software-related discipline preferred.
- 8+ years of medical device experience and 3+ years of prior team management experience.
- Medical Device Software and Quality Expertise: Deep knowledge of software development principles, ISO 13485, IEC 62304, FDA QMSR, ISO 14971, and cybersecurity requirements.
- Demonstrated experience developing software or firmware in the medical device industry, combined with software quality leadership experience and demonstrated proficiency with IEC 62304 requirements. Candidates must possess technical capability in software development, preferably C or C#, including the ability to assess code reviews, software defects, verification results, and CAPA conclusions.
- Strategic Quality Planning; Risk Management Leadership; Audit Expertise; Ability to lead strategy and provide technical direction for complex software investigations, CAPAs, quality decisions, and development-related risk assessments.
What We Can Offer You
At LivaNova, you'll help change the trajectory of lives for a new day while working alongside passionate teams dedicated to delivering impactful innovation for patients worldwide.
We offer:
- A role in an innovative medical technology environment that supports professional growth and development.
- Opportunities to collaborate with international partners and cross-functional teams to bring life-changing solutions to patients.
- A culture grounded in Empowered Accountability, Curious Mindset, Constructive Collaboration, and Thoughtful Humility.
- Competitive compensation and an inspiring place to work.
If you're inspired by purpose-driven work, meaningful innovation, and the opportunity to bring New Life in Action every day, we encourage you to apply. We look forward to hearing from you.
Valuing different backgrounds:
LivaNova values equality and diversity. We are committed to ensuring that our recruitment process is fair, transparent and free from unlawful discrimination. Our selection process is driven by the key demands/requirements for the role rather than bias or discrimination on the basis of a candidate’s sex, gender identity, age, marital status, veteran status, non-job-related disability/handicap or medical condition, family status, sexual orientation, religion, color, ethnicity, race or any other legally protected classification.
Notice to third party agencies:
Please note that we do not accept unsolicited resumes from recruiters or employment agencies. In the absence of a signed Recruitment Services Agreement, we will not consider, or agree to, payment of any referral compensation or recruiter fee. In the event that a recruiter or agency submits a resume or candidate without a previously signed agreement, we explicitly reserve the right to pursue and hire those candidate(s) without any financial obligation to the recruiter or agency.
Beware of Job Scams:
Please beware of potentially fraudulent job postings or suspicious recruiting activity by persons posing as LivaNova recruiters or employees. The scammers may attempt to solicit confidential, personal information, such as a social security number, or your financial information. LivaNova will never ask for fees prior/during/after the application process, nor will we ask for banking details or personal financial information in return for the assurance of employment. If you are concerned that an offer of employment might be a scam or that the recruiter is not legitimate, please verify by searching for “See Open Jobs” on https://www.livanova.com/en-us/careers, and check that all recruitment emails come from an @livanova.com email address.
See all 96+ H-1B Visa Software Quality Assurance Manager Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new H-1B Visa Software Quality Assurance Manager Jobs.
Get Access To All JobsTips for Finding H-1B Visa Sponsorship as a Software Quality Assurance Manager
Map your degree to QA frameworks
USCIS evaluates whether your degree directly relates to software quality assurance duties. Document how your computer science, software engineering, or IT degree applies to test planning, defect lifecycle management, and QA methodology, not just general technology work.
Verify prevailing wage before negotiating
Your employer's LCA must certify a wage at or above the DOL prevailing wage for your specific metro area and job level. Use OFLC Wage Search to look up the Level II or III rate for SOC 15-1253 before you enter salary discussions.
Target employers with multi-site QA teams
If your role involves work across multiple client or company locations, each worksite needs its own certified LCA. Prioritize employers whose QA operations are centralized or who have prior experience managing multi-location H-1B visa compliance for engineering managers.
Find sponsors through Migrate Mate by role
Search Migrate Mate to identify employers with verified H-1B LCA filing history for software quality assurance and engineering management roles. This lets you target companies that have sponsored similar positions rather than cold-applying to employers with no sponsorship track record.
Use O*NET to anchor specialty occupation evidence
The O*NET profile for Software Quality Assurance Analysts and Testers lists the degree-level knowledge domains your employer should reference when drafting the specialty occupation justification in your I-129 petition. Reviewing it helps you anticipate what USCIS will scrutinize.
Time your extension before the six-year cap
H-1B status runs up to three years and can be extended to a six-year maximum. If your employer files a PERM labor certification before you hit the five-year mark, you may qualify for extensions beyond six years, so discuss green card timelines early in the offer process.
H-1B Visa Software Quality Assurance Manager: Frequently Asked Questions
Does a Software Quality Assurance Manager role qualify as an H-1B specialty occupation?
Yes, the role typically qualifies. USCIS looks for positions requiring at least a bachelor's degree in a directly related field, such as computer science, software engineering, or information systems. A QA Manager overseeing test architecture, risk-based testing strategy, and engineering team deliverables meets that standard. Employers strengthen the petition by tying every listed duty to degree-level knowledge rather than general supervision.
Which employers sponsor H-1B visas for Software Quality Assurance Managers?
Technology companies, healthcare IT firms, financial services organizations, and enterprise software vendors are among the most active H-1B sponsors for QA management roles. The best way to identify verified sponsors is to browse Migrate Mate, which shows employers with confirmed LCA filing history for software quality assurance and related engineering management positions.
What LCA requirements apply when a QA Manager works across multiple client sites?
Each distinct worksite location requires its own certified Labor Condition Application filed with DOL before work begins at that location. A single LCA tied to your employer's headquarters does not cover unplanned client sites or project assignments at other facilities. Confirm with your employer that the LCA scope matches your actual work locations before accepting an offer.
How long does H-1B status last for a Software Quality Assurance Manager?
USCIS grants H-1B status for up to three years on the initial petition, with one extension available for a total of six years. If your employer files a PERM application or an I-140 immigrant petition before your fifth year, you may qualify for one-year or three-year extensions beyond the six-year cap while your green card case is pending.
What documents should a QA Manager prepare before an employer files the H-1B petition?
Gather your academic credentials, including transcripts and degree certificates, and have a credential evaluation completed if your degree is from outside the United States. Prepare a detailed resume that connects each QA management responsibility to degree-level competencies in software engineering or computer science. USCIS may issue a Request for Evidence if the specialty occupation tie is not clearly established from the outset.