Software Verification Engineer

EPITEC; Little Canada (MN); On-site; USD 49,593 - 52,348; Full time

Benefits offered by this job

Medical insurance

Vision insurance

401(k)

Disability insurance

Job summary

A leading medical device company in Little Canada, Minnesota seeks a Software Verification Engineer I to join their fast-paced verification team. The ideal candidate will have a Bachelor's degree in Engineering or Computer Science and experience in software testing. Responsibilities include planning and executing test cases, defect resolution, and collaborating with regulatory standards. This contract position offers comprehensive benefits including medical, vision, and 401(k) plans.

Qualifications

• Bachelor's degree in Computer Science, Computer, Electrical or Biomedical Engineering required.
• Knowledge of software testing and development lifecycle tools is essential.
• Excellent documentation and communication skills are mandatory.

Responsibilities

• Plan, write, and execute test cases according to regulatory standards.
• Design test suites for new features and functionalities.
• Record and address defects found during verification activities.

Skills

Knowledge of software testing

Excellent communication skills

Organized and detail-oriented

Analytical skills

Education

Bachelor's degree in Computer Science or Engineering

Tools

Software development lifecycle management tools

Job description

This range is provided by EPITEC. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$36.00/hr - $38.00/hr

JOB TITLE: Software Verification Engineer I

JOB TYPE: W2 Contract

LOCATION: Little Canada, Minnesota

INDUSTRY: Medical Device & Healthcare

Summary

• The Software Verification Engineer will bring testing expertise to the innovative, and fast-paced verification team.
• This high caliber, motivated and passionate individual will be responsible for requirements analysis, test design, test execution, defect issue resolution.

Responsibilities

• Work independently and as a team member to plan, write, and execute test cases according to Client's practices, FDA regulatory, and ISO standard procedures.
• Design new test suites for new features and functionality.
• Perform dry runs and formal Verification activities as required.
• Setup and configure Test Equipment.
• Record and close defects found during V&V activities.
• Perform requirements, design and tests reviews.

Experience and Education Required

• Bachelors degree in Computer Science, Computer, Electrical or Biomedical Engineering.
• Knowledge of software testing.
• Knowledge of software development lifecycle management tools.
• Organized, on-time, quick learner and detailed oriented.
• Excellent documentation skills in delivering information that adds value to managements decision-making process.
• Experienced in quantitative, analytical, organizational, and follow-up skills.
• Polished communicator - written documentation and oral presentations/ discussions/ meetings.
• Excellent reputation for building relationships across various levels of an organization.
• Energized attitude, proactive thinker and self-starter.

Seniority level

• Associate

Employment type

• Contract

Job function

• Information Technology and Engineering
• Biotechnology Research, Hospitals and Health Care, and Medical Equipment Manufacturing

Benefits

• Medical insurance
• Vision insurance
• 401(k)
• Disability insurance