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Medical Device Software Testing Jobs in Merrimack, NH

Abbott

Software Design Quality Engineer

Westford, MA · On-site

Ability to work in a lab, and hands-on experience with medical device development * Ability to ... Experience in software testing and verification/validation, including lead experience, desired ...

Abbott

Software Design Quality Engineer

Westford, MA · On-site

Ability to work in a lab, and hands-on experience with medical device development * Ability to ... Experience in software testing and verification/validation, including lead experience, desired ...

Abbott

Software Design Quality Engineer

Westford, MA · On-site

Ability to work in a lab, and hands-on experience with medical device development * Ability to ... Experience in software testing and verification/validation, including lead experience, desired ...

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Showing results 1-20

All JobsMedical Device Software Testing JobsMedical Device Software Testing Jobs in Merrimack, NH

Medical Device Software Testing information

See Merrimack, NH salary details

$19

$44

$71

How much do medical device software testing jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for medical device software testing in Merrimack, NH is $44.54, according to ZipRecruiter salary data. Most workers in this role earn between $34.23 and $53.65 per hour, depending on experience, location, and employer.

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 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, and why are they important?

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 job categories do people searching Medical Device Software Testing jobs in Merrimack, NH look for? The top searched job categories for Medical Device Software Testing jobs in Merrimack, NH are:
Medical Device Software Testing jobs near you

Software Architect

Suntra MedTech Solutions

Bedford, NH • On-site

Other

Posted 3 days ago

Job description

Description

Position Overview: Responsible for the high-level architecture and design of medical device software, ensuring alignment with system and software requirements. This "hands-on" role requires you to be in our Bedford, NH office (on a scheduled basis) to collaborate with project managers and software teams on multiple projects. The role includes reviewing detailed designs, the testing structure, and code, while also focusing on risk management and cybersecurity to ensure device safety for users and clinicians. It also offers the chance to lead technical initiatives, guide engineering teams, and make a significant impact on the development of medical devices.


Key Responsibilities:

  • Architecture & Design: Develop scalable, secure, and compliant software architecture based on system and software requirements.
  • Collaboration & Leadership: Work closely with project managers and software teams, providing architectural guidance and mentoring engineers.
  • Code Quality & Reviews: Conduct code reviews, enforce coding standards, and ensure high-quality, maintainable code.
  • Regulatory Compliance: Ensure adherence to regulatory standards (e.g., IEC 62304) for medical device software.
  • Risk Management & Cybersecurity: Integrate safety measures and conduct risk assessments to ensure device safety.
  • Continuous Improvement: Advocate for best practices, evaluate new technologies, and enhance development processes.

Requirements

Qualifications:

  • Required: Bachelor's degree in software engineering, Computer Science, Electrical Engineering, or a related field; 10+ years of industry experience; proficiency in programming languages (e.g., C, C#, C++, JavaScript); experience with embedded systems, and medical device development; familiarity with Agile/Scrum processes.
  • Beneficial: Master's degree; experience in Class B and C medical devices; Linux OS configuration; familiarity with test-driven development (TDD), CI/CD, and regulatory standards like IEC 62304.
  • Preferred: Experience using generative AI to aid in software development, developing machine learning-based products, knowledge of embedded Linux, real-time operating systems (RTOS), and cybersecurity hardening, as well as familiarity with Atlassian tools and software development best practices.

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