Senior Software Test Engineer

PSG Global Solutions

North Haven (CT)

On-site

Full time

14 days+

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Job summary

A leading medical device firm in Connecticut is seeking a Senior Software Test Engineer to work within the R&D team developing robotic surgical systems. The ideal candidate will have over 5 years of experience in FDA regulated environments, proficiency in C++, and the ability to create automated test infrastructure. Responsibilities include developing test protocols, collaborating with engineers, and ensuring software compliance with safety standards. This position is contract-based with potential for extension.

Qualifications

  • 5+ years of experience in a regulated environment.
  • Experience with FDA medical product verification.
  • Thorough understanding of creating test protocols.

Responsibilities

  • Develop and support software validation for robotic surgical systems.
  • Automate software testing for safety-critical products.
  • Collaborate with engineering teams to ensure clarity in requirements.

Skills

C++
Test automation
Verification protocols
Cross-functional collaboration

Education

BS/BA in Computer Science, Computer Engineering, or Information Technology

Tools

GMock
Vectorcast

Job description

JOB TITLE: Test Engineer III / Senior level Software Test Engineer

CLIENT: A prominent Medical Devices Company.

CONTRACT: 12 months contract (04/24/2017 to 04/23/2018) with a possibility of extension - possibility to be an employee based.

LOCATION: North Haven CT USA 06473

Pay Rate: To be discussed over the phone

1st Shift.

SUMMARY OF POSITION

This Senior Software Test Engineer will work within the R&D engineering team to develop and support the next generation robotic assisted surgical system.

This Software Test Engineer should have experience working in a fast-paced environment developing test procedures and C++ software using GMock and/or Vectorcast to automate the verification of software requirements for safety critical products.

In addition, s/he will work with cross-functional engineering teams to insure requirements are clear and testable, and be capable of reviewing test protocols and test software developed by the test engineering team.

MINIMUM REQUIREMENTS
Education required/ preferred
  • A minimum of a BS/BA in a technical discipline, preferably software related: Computer Science, Computer Engineering, Information Technology
Work Experience
  • 5 years or more experience in a regulated environment. FDA experience preferred.
  • Experience with Medical Product verification and FDA guidance.
  • Thorough understanding of creating test protocols for verifying software requirements.
  • Ability to create test automation infrastructure, and plan for automated regression testing.
  • Experience testing complex electro-mechanical devices controlled by software.
  • Experience with embedded RTOS and knowledge of C and C++.
  • Ability to manage, track and upgrade multiple hardware and software configurations.
  • Ability to work with Systems, Mechanical, Electrical and Software engineers when discovering, documenting, and resolving integration issues.
  • Understanding of IEC 62304 a strong plus.
  • Need to work well with diverse software teams, and work well in large groups.
Preferred Experience
  • Experience delivering software testing results for FDA submissions
  • Experience with GMock and/or Vectorcast
Other Skills
  • Fluency in English required
Additional Information

All your information will be kept confidential according to EEO guidelines.

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