Senior Verification Engineer

Posted 6 Days Ago
Be an Early Applicant
Boston, MA, USA
In-Office
90K-165K Annually
Senior level
Artificial Intelligence • Healthtech • Software • Cybersecurity
The Role
Plans, develops, executes, and documents verification tests for software, hardware, applications, GUIs, and embedded medical devices. Develops test plans, protocols, cases, and reports; performs risk analysis and FMEA reviews; ensures compliance with FDA design controls, ISO 13485, and IEC 62304. The role also supports test automation, issue tracking, client relationships, project milestones, and continuous improvement of verification practices.
Summary Generated by Built In

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. 
The final salary offer is determined by factors such as experience, location, skills, education, and market conditions. **

Skills Required

  • 5-10 years of experience as a verification engineer
  • Experience with verification and validation planning
  • Experience developing test cases, test protocols, test plans, and test reports
  • Understanding of FDA design controls and software verification and validation for medical devices
  • Understanding of IEC 62304 and applicable medical device standards
  • Experience with software, hardware, application, GUI, or back-end testing
  • Experience with requirements review and allocation
  • Experience with issue tracking and bug tracking tools
  • Experience reviewing risk analysis and FMEA related to test failures
  • Understanding of software development lifecycle and Agile development
  • Experience with test tools and test automation
  • Experience developing test cases and protocols for medical device applications
  • Experience writing formal test reports compliant with Good Documentation and Good Laboratory Practices
  • Experience writing automated test scripts
  • Experience with products reviewed or certified by test houses or notified bodies
  • Experience using LabVIEW or a similar environment for system verification
  • Experience with performance testing of medical device systems
  • Statistics experience, including sample size determination
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The Company
HQ: Southborough, Massachusetts
69 Employees
Year Founded: 1982

What We Do

Full Spectrum offers complete product development and testing services for Medical Device, Life Sciences, Evolving Healthcare , and Regulated Robotics. We have successfully completed over 1,000 development programs in our 40+ year history, including class III medical devices, highly efficient robotics, complex algorithm based systems and more.. ⦁ ISO 13485 certified since 2009 ⦁ Successfully in business since 1982

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