Description

Execute software verification activities for a medical device system in Westford, MA.

You will own requirements analysis, test design, execution, and defect resolution for FDA-regulated projects.

Responsibilities

• Lead testing projects including estimation, planning, and daily task coordination.
• Write and execute test cases compliant with FDA regulatory and ISO standards.
• Participate in requirements, hazard analysis, and design reviews for new features.
• Evaluate and recommend software test tools to ensure quality.

Required Skills

• 5+ years of professional software test engineering experience.
• Bachelor's degree in Computer Science or equivalent.
• Proficiency in test designs and defect reviews.
• Strong understanding of software development lifecycles and workflows.
• Experience with software development lifecycle management tools.
• Proven project management and leadership skills.
• Excellent documentation skills for management decision-making.

Key Skills

Education

Bachelor's Degree