New · posted Nov 7
LivaNova · Medical Devices
Senior Manager, Software Quality Assurance
- Remote, Texas, US
- Remote
- Full-time
- Manager
The role
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.
What you need
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 you'll do
- 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.
Pay and benefits
$150,000 – $175,000 a year
Employer providedAs 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.
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 you 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 the improve user experience. LivaNova is a growing, cutting-edge, medical device company specializing in neuromodulation product the enrich patients lives.
Discretionary annual bonus
Competitive compensation
Professional growth and development
Equal opportunity, accessibility and legal noticesLivaNova's statements, word for word
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.
Job intelligence
The context around this role
Live data · November 7, 2026
Salary intelligence
How the pay compares
This roleEmployer provided
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $150,000 | — | $175,000 |
This role: LivaNova's own published range.
Career trajectory
Where this role sits in Software Quality & CSV
The general path across 55 open Software Quality & CSV roles on Regulatory Jobs, with the titles they carry most. Not LivaNova's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 25 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership14
- Data and digital systems10
- Quality systems and risk7
- GMP and compliance3
- Investigations and CAPA3
- Lab testing and methods2
- Documentation and SOPs2
- Validation and qualification2
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Software Quality & CSV work in medical devices, led by the four this posting names, each linked to the agency or standards body that publishes it.
- IECIEC 62304(official source, opens in a new tab)Software life cycle processes for medical device softwareNamed in the posting
- FDA21 CFR Part 820 (QMSR)(official source, opens in a new tab)FDA quality management system regulation for medical devices, aligned with ISO 13485Named in the posting
- ISOISO 13485(official source, opens in a new tab)Quality management systems for medical devicesNamed in the posting
- ISOISO 14971(official source, opens in a new tab)Application of risk management to medical devicesNamed in the posting
- FDAFDA Computer Software Assurance(official source, opens in a new tab)Risk-based assurance for production and quality system software
- FDA21 CFR Part 11(official source, opens in a new tab)FDA rules for electronic records and electronic signatures
- FDAFDA cybersecurity in medical devices(official source, opens in a new tab)Quality system considerations and premarket content for device cybersecurity
- FDAFDA Investigations Operations Manual(official source, opens in a new tab)How FDA investigators plan and conduct inspections
- ISOISO 19011(official source, opens in a new tab)Guidelines for auditing management systems
- FDA21 CFR Part 7(official source, opens in a new tab)FDA enforcement policy, including product recalls
- FDA21 CFR Part 56(official source, opens in a new tab)Institutional review boards for FDA-regulated clinical investigations
- ISPEISPE GAMP 5(official source, opens in a new tab)A risk-based approach to compliant GxP computerized systems
- IMDRFIMDRF(official source, opens in a new tab)International Medical Device Regulators Forum guidance, including software as a medical device
- IECIEC 62366-1(official source, opens in a new tab)Application of usability engineering to medical devices
- EUEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation: CE marking, technical documentation, vigilance
- HHSHIPAA Privacy Rule(official source, opens in a new tab)Federal protections for individually identifiable health information
Company hiring pulse
LivaNova on Regulatory Jobs
- 6
- Open roles
- 6
- Distinct roles
- 2
- Locations
By discipline
- Quality4 67%
- Regulatory1 17%
- Clinical1 17%
By level
- Manager3 50%
- Associate & Specialist2 33%
- Senior & Principal1 17%
More roles at LivaNova
- View role
Senior Manager, Clinical Operations Programs
Remote, Texas, USManagerMedical Devices$160K–$190K
- View role
Quality Engineering Intern
Arvada, COAssociate & SpecialistMedical Devices$52K
- View role
Quality Engineer
Arvada, COAssociate & SpecialistMedical Devices$75K
- View role
Senior Quality Engineer
Arvada, COSenior & PrincipalMedical DevicesSalary not listed
Senior Manager, Software Quality Assurance at LivaNova
Open until filled. $150K–$175K a year, employer provided.