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Medical Device Software Testing Jobs in Massachusetts

... in testing processes, efficiency, and integration within Agile workflows. Qualifications: * 10 years experience executing Verification & Validation (V&V) strategy for Software as a Medical Device ...

... medical device regulations. * Maintain accurate and traceable software test records in accordance ... Apply risk-based testing strategies to prioritize high-impact product functionality and patient or ...

Senior Software Engineer

Andover, MA · On-site

$129 - $184/hr

Integration of testing, static analysis, and security frameworks, a plus. * Medical device software development experience with compliance to IEC-62304 and FDA guidelines. * Must be team-oriented ...

Showing results 21-40

Medical Device Software Testing information

What is medical device software testing?

Medical device software testing is the process of verifying and validating the software used in medical devices to ensure it is safe, reliable, and compliant with regulatory standards. This involves various testing methods, such as functional, performance, and usability testing, to identify and fix potential issues before the device is released to the market. Proper software testing helps prevent device failures that could harm patients and ensures that the device operates as intended under all expected conditions.

What are the key skills and qualifications needed to thrive as a medical device software tester?

To excel as a Medical Device Software Tester, you need a strong background in software testing methodologies, knowledge of regulatory standards like IEC 62304, and a degree in computer science or engineering. Familiarity with testing tools such as Selenium, Jira, and automated test frameworks, as well as experience with validation and verification documentation, is typically required. Attention to detail, analytical thinking, and effective communication are crucial soft skills that help testers identify issues and collaborate with cross-functional teams. These skills and qualifications are vital to ensure the safety, reliability, and compliance of medical device software in a highly regulated industry.

What are some common challenges faced by professionals in medical device software testing, and how can they be addressed?

Professionals in medical device software testing often encounter challenges such as ensuring compliance with strict regulatory standards (like FDA or ISO 13485), managing complex documentation requirements, and keeping up with frequent software updates. Addressing these challenges requires a strong focus on detail, thorough understanding of relevant regulations, and effective communication with development and quality assurance teams. Collaborating closely with cross-functional teams and maintaining up-to-date knowledge of regulatory changes are key to successfully navigating these demands.

What is the difference between Medical Device Software Testing vs Medical Device Quality Assurance?

AspectMedical Device Software TestingMedical Device Quality Assurance
CertificationsISTQB, CSTE, or similar testing certificationsISO 13485, CAPA, or quality management certifications
Work EnvironmentTesting labs, development teams, regulated environmentsQuality management systems, compliance departments
Employer & Industry UsageMedical device companies, software developersManufacturers, regulatory agencies, compliance firms
Search & Comparison IntentUnderstanding testing roles, skills, and responsibilitiesUnderstanding quality assurance processes, compliance standards

Medical Device Software Testing focuses on verifying and validating software functionalities to ensure safety and compliance. Medical Device Quality Assurance encompasses broader quality management practices, including process audits and compliance to standards. Both roles are essential in the medical device industry but serve different purposes in ensuring product safety and regulatory adherence.

What cities in Massachusetts are hiring for Medical Device Software Testing jobs?

Cities in Massachusetts with the most Medical Device Software Testing job openings:

Infographic showing various Medical Device Software Testing job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 12% Part Time, and 6% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution.

Principal Software Test Lead

Haemonetics Software Solutions

Boston, MA • On-site

$103.60 - $176.40/hr

Other

Retirement

Posted 3 days ago

New


Job description

We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further—Haemonetics is your employer of choice.

Senior technical leader responsible for defining and executing Verification & Validation (V&V) strategy for Software as a Medical Device (SaMD) and SaaS platforms. Drives regulatory compliance, quality metrics, traceability, and scalable test automation in a regulated Agile environment. Provides technical leadership for software quality, ensuring alignment with FDA expectations and Haemonetics quality standards.

Responsibilities
  • Lead and define software V&V strategy for both non‑medical and medical device software.
  • Drive compliance with FDA design controls, IEC62304, ISO14971, and quality management systems.
  • Provide technical leadership, mentorship, and review of V&V deliverables to ensure rigor, quality, and consistency across programs.
  • Develop and implement robust test plans and test cases tailored to product and project needs.
  • Oversee test design, execution, and V&V across API, UI, backend, and integrated systems.
  • Develop and implement automated testing strategies, promote a culture of automation.
  • Establish, track, and report software quality metrics to drive data‑informed decisions.
  • Diagnose, document, and troubleshoot systems to resolve problems identified through testing and see them through to a successful resolution.
  • Recommend adjustments to resolve software issues and improve the functionality of existing software.
  • Create and maintain traceability matrices linking requirements, risks, and verification and validation activities.
  • Provide technical leadership and mentorship to engineers on V&V, compliance, and best practices.
  • Collaborate cross‑functionally with Development/Architecture teams, QA, Product Owners, and Business stakeholders to ensure comprehensive test coverage, conduct risk assessments, and drive defect resolution.
  • Support audits, submissions, and inspections with complete, accurate, and traceable documentation.
  • Drive continuous improvement in testing processes, efficiency, and integration within Agile workflows.
Qualifications
  • 10+ years of experience executing V&V strategy for Software as a Medical Device (SaMD) and SaaS platforms.
  • Bachelor’s or Master’s degree in Engineering, Computer Science, or related field.
  • Strong expertise in test automation, quality metrics, and Agile methodologies.
  • Hands‑on experience with traceability matrices and compliance frameworks.
  • Experience with SaaS/cloud‑based systems.
  • Proven leadership in mentoring and guiding engineering teams.
  • Strong analytical, problem‑solving, and communication skills.
Pay Transparency

The base pay actually offered to the successful candidate will take into account, without limitation, the candidate’s location, education, job‑knowledge, skills, and experience in prior relevant roles. Incentives may also be provided as part of Haemonetics’ employee compensation. For non‑sales roles, employees will be eligible for a discretionary annual bonus, the target amount of which varies based on the applicable role, to be governed by the applicable plan terms. Employees may also be eligible to participate in the Company’s long‑term incentive plan, with eligibility and target amount dependent on the role. The base salary range for this role is: $103,600.00–$176,400.00 per annum.

Benefits
  • 401(k) with up to a 6% employer match
  • Employee stock purchase plan
  • Flexible time off for salaried employees; accrual of three to five weeks of vacation annually (based on tenure) for hourly employees
  • Accrual of up to 64 hours of paid sick time annually
  • Paid and/or floating holidays
  • Parental leave
  • Short‑ and long‑term disability insurance
  • Tuition reimbursement
  • Health and welfare benefits
EEO Policy Statement

Equal Employment Opportunity is a core value at Haemonetics. We are committed to a workplace that reflects fairness and respect for all employees and aspiring applicants. All decisions regarding employment are based on merit and qualifications without regard to race, color, religion, sex, national origin, age, disability, protected veteran status, or any other characteristic protected by law.

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