Insulet Corporation

Sr Manager, Software Test Engineering

Insulet Corporation$169K — $253K *
Healthcare
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's or master's degree in computer science, engineering, or a related field.
  • 8-12+ years of experience in software testing, including 4+ years in a leadership role.
  • Strong expertise in test automation frameworks and performance testing.
  • Proven experience managing large, cross-functional testing teams.
  • Excellent communication and decision-making skills.

Responsibilities

  • Lead the software testing team, ensuring compliance with FDA standards for software verification.
  • Oversee multiple teams of Manual and SDET test engineers.
  • Manage Design Control and Software Test initiatives for FDA Class II and III medical devices.
  • Collaborate with project management to optimize schedules and testing processes.
  • Create and ensure compliance of documentation with regulatory requirements and standards.

Benefits

  • Medical, dental, and vision insurance.
  • 401(k) with company match.
  • Paid time off (PTO).
  • Employee wellness programs.
Full Job Description
Job Summary
Position Overview

The Senior Software Test Manager leads the overall quality strategy and execution for software releases. This role manages multiple testing teams, drives test planning and automation initiatives, and ensures high quality, on time delivery of complex software products. The manager partners closely with engineering, product, and cross functional teams to align on release goals, mitigate risks, and maintain strong quality standards. Responsibilities include team leadership, process improvement, resource planning, and oversight of all testing activities across manual, automated, integration, and performance testing. Strong communication, technical depth, and strategic planning are essential.

Responsibilities
• Manage the software testing team and ensure Software verification is conducted in accordance with the FDA standards to deliver high quality software.
• Manage multiple teams of Manual/SDET test engineers.
• Mange Design Control and Software Test initiatives to develop appropriate Design History File documents for FDA Class II and Class III medical devices.
• Responsible for the generation, review and approval of design control documentation with primary focus on software test deliverables.
• Collaborate with Project Management to support and optimize the schedules.
• Support software development teams on the validation of software tools.
• Work with software, hardware, user experience, marketing, manufacturing, and quality assurance on generation, documentation, verification and validation of requirements.
• Lead the creation of necessary documentation to comply with regulatory requirements and industry best practices.
• Establish and maintain software test programs, processes, procedures and controls to ensure compliance with FDA regulations and established standards such as IEC 62304.
• Ensures compliance to IEC 62304, and FDA Guidance on Software Contained in a 510(k) Submission.
• Provide guidance and participate in software development activities including design and code reviews, requirements analysis and tracing, defect tracking and configuration management, review requirements, specifications, product design documents, validation protocols, test plans, test cases, and other documentation as required and provide timely feedback.
• Applies a good working knowledge of Software Development Life Cycle (IEC 62304), Design Controls (ISO 13485) and other regulatory requirements and agencies as it relates to software test activities in software development.
• Work closely with the software development team to identify improvements.
• Influence the requirements definition and software design to maximize testability.
• Oversee and influence development of test objects to meet needs of protocol.
• Develop and extend protocols and plans as device features evolve.
• Participate in product design reviews.
• Represent software test in the core team meetings.
• Creating and executing test plans, test designs and test cases and generating test reports.
• Creating and updating Trace matrices between requirements and Tests.
• Work with the scrum Master and product owners to prioritize or deprioritize the backlog.
• Keep track of the Testing board and tools inventory for the team.
• Performs other duties as required.
Required Leadership/Interpersonal Skills & Behaviors
• Self-motivated
• Proactive
• Quick learner
• Mentor
• Ability to represent the team cross functionally.
• Generate metrics for the team as required.

Required Skills and Competencies
• Bachelor's or master's degree in computer science, Engineering, or related field.
• 8-12+ years of experience in software testing, including 4+ years in a leadership or management role.
• Strong expertise in test automation frameworks, performance testing, and modern QA methodologies.
• Proven experience managing large, distributed, or cross functional testing teams.
• Excellent communication, stakeholder management, and decision making skills.
• Deep understanding of SDLC, Agile methodologies, and CI/CD pipelines.
• Experience with AI assisted testing tools is a strong plus.

Education and Experience
• BS in Software Engineering, Computer Science or similar field; 12+ years hands on experience in software testing in regulated industry and/or equivalent combination of education and experience.
• Experience of 2+ years being the Software Test Manager.
• Thorough understanding of software test 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 software test tools.
• Proven record developing and executing software test protocols for complex medical devices.
• Familiarity with IEC 62304, ISO 14971, FDA regulations and international standards applicable to medical device software development, verification and validation a plus.
• Experience working with products from the prototype through 510(k)/ISO clearance and commercialization is preferred.
Additional Information
• The position is hybrid.
• Travel is estimated at 0% but will flex depending on business need.

Additional Information:
Compensation & Benefits:For U.S.-based positions only, the annual base salary range for this role is $169,100.00 - $253,625.00This position may also be eligible for incentive compensation.We offer a comprehensive benefits package, including:• Medical, dental, and vision insurance• 401(k) with company match• Paid time off (PTO)• And additional employee wellness programsApplication Details:This job posting will remain open until the position is filled.To apply, please visit the Insulet Careers site and submit your application online.Actual pay depends on skills, experience, and education.

About Insulet Corporation

Insulet Corporation is a medical device company that develops, manufactures, and sells insulin delivery systems for people with insulin-dependent diabetes. The company's flagship product, the Omnipod Insulin Management System, is a tubeless insulin pump that is worn on the body and controlled wirelessly by a handheld device. Insulet Corporation is headquartered in Acton, Massachusetts.
Learn more about Insulet Corporation
Size
2,300 employees
Market Cap
$20.6 billion
Industry
Net Income
$6.8 million
5 Year Trend
+24.5%
Revenue
$904.4 million
NASDAQ

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