Senior Verification Engineer

Socket.dev; Boston (MA); On-site; USD 90,000 - 165,000; Full time

Job summary

Full Spectrum is seeking a Sr. Verification Engineer to lead testing for medical device software and hardware. This role focuses on V&V planning, creating test methods, protocols, and execution within quality standards.

Responsibilities include developing manual test cases, writing verification documentation, coordinating with environments, and ensuring adherence to ISO 13485, IEC 62304, and FDA design controls while collaborating with clients to deliver robust solutions.

Qualifications

• 5–10 years of experience as a verification engineer.
• Experience with FDA-regulated medical devices and design controls.
• Knowledge of ISO 13485 and IEC 62304 compliance.
• Experience with test planning and protocol development.
• Ability to review risk analyses and FMEA related to testing.

Responsibilities

• Estimate, plan, develop, execute, and maintain manual test cases and test protocols.
• Write documentation including testing plans and verification protocols.
• Work with different test environments to execute test cases.
• Perform software, hardware, GUI and back-end testing.
• Design functional tests based on system specifications.
• Coordinate with project management to meet milestones.

Skills

Test case development

V&V planning

Test automation

Software testing

Agile development

IEC62304

Tools

LabVIEW

Bug tracking

Job description

Technology has never been more present in our lives than today. Everything from connected medical devices to robotics to mobile apps are becoming more a part of daily life. A career at Full Spectrum will allow you to be at the cutting edge of engineering driven innovation. If it excites you to develop new products and learn new technologies on a regular basis from a diverse set of customers, then this is the place for you.

We have a passionate team of experienced professionals who have first-hand experience developing products. Our clients are dependent on us to develop their next innovative product to bring to market. Come help us build the future, come join Full Spectrum!

Sr. Verification Engineer:

A Verification Engineer is a technical position responsible for testing and verification of software as a medical device, medical device systems and software embedded medical devices. Verification Engineers are responsible for V&V planning, mapping of test types, associating design requirements into test groups, developing test method and test cases to verify requirements, creating protocols and execution/documentation of verification tests within schedule constraints, meeting quality standards and goals.

ROLE RESPONSIBILITIES:

• Estimate, plan, develop, execute, and maintain manual test cases and test protocols for products under development.
• Writing skills to develop documentation including testing plans, detailed test cases, and verification protocols.
• Work with different Test Environments to execute the test cases.
• Perform Software, Hardware, Application, GUI and/or Back-End testing.
• Design and develop functional tests based on system specifications.
• Work with project management to meet the testing milestones and deliver high quality solutions on time.
• Ensure that FDA-regulated medical products are tested in adherence to the applicable standards, regulations (ISO 13485, IEC 62304) and best practices.
• Manage relationships with clients
• Contributing to the continuous improvement of verification engineering practices
• Identify opportunities to drive further value in client engagements
• Reviewing risk analysis and experience working on FMEA's as it relates to test failures
• Understanding of FDA design controls and Software V&V for medical devices
• Understanding of standards impacting verification of medical devices such as IEC62304
• Understanding of issue tracking, issue tracking process and management of issues list in a bug tracking tool
• 5-10 years experience as a verification engineer

PREFERRED EXPERIENCE:

• Test case and protocol development for medical device applications. Experience writing formal test reports that meet Good Documentation and Lab practices.
• Experience writing test scripts with creating Automated Test cases a plus.
• Experience with software or medical devices that have been reviewed or certified by test houses or notified bodies.
• Use of LabVIEW or similar environment to aid in verification of systems. Author automated Test Scripts a plus.

Knowledge, Skills and Abilities:

• Writing test cases, protocols
• Test case development for GUI and GUI workflows
• Negative and positive testing for functional test cases
• Test planning, protocol writing
• Test report writing.
• Requirements review an allocation
• V&V planning experience
• Test tools and test automation experience
• Understanding of software Development lifecycle and Agile development
• IEC62304
• Performance testing medical device systems
• Statistics experience, sample size determination

The base salary for this position is $90,000 to $165,000 annually, and the role is bonus eligible.