Principal I, Research & Development Quality Assurance (T)

Summary of Position: We are seeking a Quality Assurance Engineer to provide QA oversight for Digital Health software tools and customer‑facing supporting software systems and infrastructure within a regulated environment.  In this role, you will work closely with IT, software development, and business teams to ensure systems are developed, tested, changed, migrated, and maintained in compliance with 21 CFR Part 11, GAMP, Computerized System Validation (CSV) / Computer Software Assurance (CSA), ISO 13485, and applicable GxP expectations, using an Agile delivery model.  This role focuses on quality oversight, review, assessment, and approval of testing and validation activities, rather than execution of hands‑on testing.  This role supports global teams across the USA (Central and Pacific time zones) and India (IST) and requires flexibility to collaborate across time zones.  Key Responsibilities:  Provide QA oversight for Digital Health software tools and customer‑facing supporting software systems and infrastructure  Apply CSV and CSA risk‑based approaches to review and assess validation and testing strategies  Perform GxP and impact assessments to help determine validation scope and testing needs  Assess and support change control activities, including validation and risk impact assessments  Ensure systems remain in a validated state throughout their lifecycle through oversight and governance  Integrate QA and validation oversight activities into Agile sprints and releases  Review requirements and user stories for quality, testability, and traceability  Review and approve testing evidence, defect assessments, and retesting outcomes as appropriate  Collaborate with IT and development teams to support compliant system delivery  Support audit and inspection readiness activities as needed  Provides strategic guidance for post-market support activities  Operates independently on complex tasks and contributes to critical QA technical decisions.   Key Requirements/Minimum Qualifications: Bachelor’s degree in engineering, computer science, life sciences, or a related field  5+ years relevant experience. Experience in software QA or validation within a regulated environment  Working knowledge of CSV, CSA, and 21 CFR Part 11  Experience performing change control and impact assessments  Experience supporting GxP systems  Experience working in an ISO 13485 medical device environment  Familiarity with Agile development environments  Ability to work effectively with global, cross functional teams  Preferred Qualifications/Skills/Experience  Experience supporting systems used in IT development or cloud operations  Familiarity with Agile tools such as Jira or ServiceNow  Experience supporting audits or regulatory inspections  Strong communication and collaboration skills  Work hours: 1 PM to 10 PM IST Relocation assistance: Yes