Hybrid Senior SW Tools Test Engineer

at Diabetes Youth Families

• Job title: Senior SW Tools Test Engineer
• Job type: Full Time
• Experience level: Senior
• Salary: $94,725 - $142,087 per year
• Degree requirement: Bachelor's Degree
• Tech skills: SDLC
• Location requirements: Hybrid, Acton, United States

About the role

• Senior Software QA Engineer validating non-product custom tools at Insulet Corporation. Collaborating with cross-functional teams and ensuring compliance with regulatory standards in medical device development.

Responsibilities

• Lead the validation efforts for non-product custom tools used within the Pod Software Group.
• Develop and execute comprehensive test plans, test cases, and test scripts.
• Collaborate with cross-functional teams, including software development, DevOps, Automation, and product management, to ensure tool quality and functionality.
• Identify, document, and track defects, and work with development teams to resolve issues.
• Ensure compliance with regulatory standards and company policies.
• Provide mentorship and guidance to junior SQA team members.
• Continuously improve testing processes and methodologies.

Requirements

• BS in Software Engineering, Computer Science or similar field
• 5+ years’ hands on experience in software quality assurance associated with real-time embedded software systems in regulated industry and/or equivalent combination of education and experience.
• Strong understanding of the Software Development Life Cycle (SDLC) and quality assurance methodologies.
• Proficiency in manual testing tools and approaches.
• Excellent problem-solving skills and attention to detail.
• Strong communication and collaboration skills.
• Thorough understanding of software quality assurance principles, practices, and metrics, as well as software development and testing best practices that foster high-quality software.
• Hands-on experience using modern software development and quality assurance tools.
• Proven record of developing and executing software test protocols for complex medical devices.
• Automation experience (preferred).
• Experience with DevOps practices and tools (preferred).
• Knowledge of regulatory standards in the medical device industry (preferred).
• Experience working with products from prototype through 510(k)/ISO clearance and commercialization (preferred).

Benefits

• Hybrid working arrangements (requires on-site work from our Acton, MA office; may work remotely other days)