Software Quality Assurance Senior Manager

Nova Biomedical Corporation • Waltham, MA

2d • Onsite

About The Position

The Software Quality Assurance Senior Manager leads the software quality organization responsible for ensuring the safety, reliability, and regulatory compliance of software used in medical device systems. This role oversees verification and validation activities across embedded firmware and cloud-based applications, ensuring compliance with IEC 62304 and related regulatory standards. The position bridges engineering, regulatory, and business teams to deliver audit-ready software solutions used in clinical environments. The Senior Manager drives continuous improvement through automation, modern tooling, and AI-enabled quality practices. If youre passionate about SQA and want to be part of a team that is shaping the future of life sciences, wed love to hear from you, apply today!

Requirements

• Minimum of 10 years of experience in Software Quality Assurance, including at least 7 years in a leadership or management role within the medical device, healthcare, or similarly regulated industry.
• Deep expertise in IEC 62304, ISO 13485, FDA 21 CFR Part 11, and IVDR regulatory requirements.
• Demonstrated experience testing embedded systems, cloud-based applications, and hybrid edge-to-cloud architectures.
• Proven ability to design, implement, and maintain automated test frameworks for embedded firmware and web-based APIs.
• Experience operating within regulated CI/CD environments such as Jenkins, GitLab, or Azure DevOps.
• Strong analytical, problem-solving, and communication skills, with the ability to translate technical and regulatory risks into business-relevant terms.
• Solid understanding of cybersecurity principles and cybersecurity testing practices.
• Bachelors degree in Computer Science, Biomedical Engineering, or a related technical field required.
• Ability to work for prolonged periods at a laptop or desktop computer.
• Ability to lift and carry up to 15 pounds.
• Ability to wear required personal protective equipment (PPE) as necessary.

Nice To Haves

• Masters degree preferred or an equivalent combination of education and professional experience.

Responsibilities

• Lead the development and execution of software verification and validation (V&V) strategies to ensure
• Lead the development and execution of software verification and validation (V&V) strategies to ensure compliance with IEC 62304, ISO 13485, FDA 21 CFR Part 11, and IVDR requirements.
• Oversee software testing activities across embedded diagnostic hardware, firmware, and cloud-hosted applications that process and store patient data.
• Ensure end-to-end traceability between software requirements, risks, test cases, and defects using ALM and issue-tracking tools such as Jama Connect and Jira.
• Drive modernization of software quality practices by transitioning from manual-heavy testing approaches to automation-first strategies.
• Pilot and implement AI-assisted tools to support test plan development, edge-case generation, and predictive defect analysis.
• Manage, mentor, and develop Software Development Engineers in Test (SDETs) and QA Engineers, fostering a proactive and accountable quality culture.
• Communicate software quality risks, test results, and regulatory readiness to engineering leadership and cross-functional stakeholders.
• Perform other duties as assigned.

Benefits

• Flexible Medical, Dental, & Vision Coverage
• Competitive 401k company match
• Bonus Program, Generous PTO and paid holidays
• Generous Tuition reimbursement
• Hybrid and flexible work arrangements
• Professional development, engagement and events
• Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices
• Company subsidized cafeteria in our Waltham, MA office

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level