Lead QA Engineer overseeing test planning and execution for Salesforce applications in a fast - paced environment. Collaborating with multiple teams to guarantee quality and adherence to standards.
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)
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