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Medical Device Software Qa Manager Jobs (NOW HIRING)

This role is instrumental in ensuring software solutions are secure, maintainable, testable, and compliant with applicable federal and organizational standards. Responsibilities: Lead quality ...

Quality Assurance Manager

Nashville, TN ยท On-site

$75K - $90K/yr

Our client is seeking a Quality Assurance Manager responsible for developing and implementing ... Minimum 5 years proven experience in the medical device industry. Minimum 2 years of experience in ...

... medical device companies and 9 of the top 10 pharmaceutical companies.Reporting to the General ... The QA Manager maintains responsibility for all aspects connected with compliance, including the ...

Understand medical device risk management concepts and their application to the product firmware ... Software Quality Assurance - Non-product software * Ensure non-product software systems are ...

... care medical device solutions used in the detection of infectious disease such as COVID-19 ... Experience with QMS software and documentation systems is a plus. Certifications: * ASQ ...

Proactively engage in the end-to-end software testing cycle as it pertains to the project. * Work closely with and follow direction from QA Manager * Contribute to the establishment of and meet ...

Short-Term Consulting Engagement We're looking for an experienced Software QA Consultant to help us ... Experience with QA management or technical leadership. * Experience with enterprise SaaS ...

Short-Term Consulting Engagement We're looking for an experienced Software QA Consultant to help us ... Experience with QA management or technical leadership. * Experience with enterprise SaaS ...

Analyze testing results, identify trends and risks, and communicate project status and QA findings to the Software Quality Assurance Manager. * Clearly document software defects, issues, and ...

New

Maintain and ensure our Quality Management System (QMS) for compliance with AS 9100 and CMMI ... medical conditions), sexual orientation, gender identity, gender expression, age, status as a ...

Maintain and ensure our Quality Management System (QMS) for compliance with AS 9100 and CMMI ... medical conditions), sexual orientation, gender identity, gender expression, age, status as a ...

$123K - $196K/yr

... medical device software. * Direct, hands-on experience implementing and maintaining quality ... Experience working with electronic Quality Management Systems (eQMS), such as Greenlight Guru ...

Director Quality Assurance

Cleveland, OH ยท On-site

$123K - $196K/yr

... medical device software. * Direct, hands-on experience implementing and maintaining quality ... Experience working with electronic Quality Management Systems (eQMS), such as Greenlight Guru ...

Minimum Qualifications: * 7+ years of experience in software quality assurance, with at least 2 ... medical condition, genetic information, protected veteran status, sexual orientation, gender ...

... and medical benefit administration on a single, secure platform. By delivering true price ... software development lifecycle. The QA Manager works closely with product, engineering, and ...

Showing results 21-40

Medical Device Software Qa Manager information

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$12K

$118.6K

$166.5K

How much do medical device software qa manager jobs pay per year?

As of Sep 9, 2026, the average yearly pay for medical device software qa manager in the United States is $118,644.00, according to ZipRecruiter salary data. Most workers in this role earn between $110,000.00 and $139,500.00 per year, depending on experience, location, and employer.

What are popular job titles related to Medical Device Software Qa Manager jobs?

For Medical Device Software Qa Manager jobs, the most frequently searched job titles are:

Infographic showing various Medical Device Software Qa Manager job openings in the United States as of July 2026, with employment types broken down into 77% Full Time, 14% Part Time, and 9% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $118,644 per year, or $57 per hour.

Cybersecurity and Data Protection Software Quality Engineer

Boston, MA โ€ข On-site

Foundation Medicine
Biotechnology Research and Developmentย โ€ขย 1 - 5K employees

$93K - $116K/yr

Other

Re-posted 29 days ago


Job description

About the Job

At Foundation Medicine, we value our cybersecurity team as the first โ€” and last โ€” line of defense in protecting our sensitive data from cyberattack. The Software Quality Engineer is an experienced and vigilant Software Quality Professional responsible for ensuring that FMI softwareโ€‘enabled medical devices, and software supporting the FMI quality system are compliant with the cybersecurity expectations of our patients, physicians, partners and regulators, prevents breaches of all sizes, understands when they occur, and takes immediate steps to remediate them. In this role, the Software Quality Engineer is the bridge between FMI Product Owners, Software Owners, Software Engineering, Information Technology, Data Privacy and Regulatory Affairs, ensuring "security by design" and data protection are embedded into the FMI Quality Management System (QMS).

The role will lead efforts to implement a Secure Product Development Framework (SPDF) and prepare documentation to support premarket submissions (De Novo, PMA, 510(k)). This individual has an understanding of cybersecurity standards and certifications in regulated healthcare, extensive knowledge of how cybercriminals work, and determination to never allow them access.

Key Responsibilities
  • Regulatory Alignment & QMS Management: Provide guidance on QMS procedures to align with identified cybersecurity protection requirements, specifically integrating SPDF, threat modeling, and SBOM management into existing FMI Design Controls.
  • Premarket Submission Support: Review and approve comprehensive cybersecurity documentation for regulatory compliance, including Security Risk Management Reports, Threat Models, and Security Architecture views.
  • Software Bill of Materials (SBOM) Management: Ensure the development and maintenance of compliant, machineโ€‘readable SBOM (e.g., SPDX or CycloneDX) for all software components, tracking vulnerabilities (CVEs) and managing supplier risks.
  • Risk Assessment & Verification/Validation Oversight: Collaborate with Product Owners, System Owners, Information Security and Data Privacy to conduct cybersecurity risk assessments. Review and approve Cybersecurity and Data Protection requirements and verification results (vulnerability analysis, penetration testing) to ensure compliance with preโ€‘determined acceptance criteria.
  • Postโ€‘market Surveillance & Patching: Support the development and implementation of a comprehensive postโ€‘market, software system cybersecurity vulnerability monitoring plan. Review and approve SOPs for timely patching and updating of fielded devices.
  • Crossโ€‘Functional Collaboration: Act as the subject matter expert (SME) advising FMI stakeholders on cybersecurity and data protection on medical device regulations, guidanceโ€™s, conformity and reference standards, and best practices during the entire Software Development Lifecycle (SDLC).
  • Audit Preparation: Support internal and external audits (FDA, Notified Bodies) regarding software validation and cybersecurity compliance.
  • Supplier Management: Collaborate with Product Owners, System Owners, Information Security and Data Privacy in the identification, selection and onboarding and management of suppliers to ensure that suppliers are capable of meeting the cybersecurity and data protection requirements of FMI.
  • Quality Management System: Maintain documentation of security guidelines, procedures, standards, and controls.
Qualifications

Basic Qualifications:

  • Bachelorโ€™s degree (or equivalent) in information systems, information technology, or related field.
  • 2+ years of experience in software quality assurance or cybersecurity at a midsize or large company in the healthcare or other regulated space.
  • Deep knowledge of IT, including hardware, software, and networks.
  • Direct experience with regulatory or notified body cybersecurity submissions.
  • Experience with ISO 13485, IEC 62304 (Medical Device Software Lifecycle), and ISO 14971 (Risk Management).

Preferred Qualifications:

  • Meticulous eye for detail and an ability to multitask in a fastโ€‘paced environment.
  • Strong abilities in critical thinking, problemโ€‘solving, logic, and forensics.
  • Excellent verbal and written communication skills.
  • Ability to work successfully in both individual and team settings.
  • Ability to think like a hacker in order to stay ahead of threats.
  • Understanding of HIPAA and importance of patient safety and data privacy regulations and guidelines.
  • Commitment to reflect FMIโ€™s values: Integrity, Courage, and Passion.

The expected salary range for this position based on the primary location of Boston, MA is $93,500 โ€“ $116,500 per year. The salary range is commensurate with Foundation Medicineโ€™s compensation practice and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for Foundation Medicineโ€™s benefits.

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