{"id":3146584,"url":"https://alion.io/job/selective-global-search-senior-software-verification-validation-engineer-medical-devices","title":"Senior Software Verification & Validation Engineer - Medical Devices","company":{"id":4465183,"name":"Selective Global Search","domain":"selectiveglobalsearch.com","url":"https://alion.io/company/selective-global-search","size_band":null,"is_staffing_agency":true,"employer_type":"agency","is_intermediary":false,"listed_via":null,"ats_vendor":null,"truth_index":null},"role":"Backend","role_family":"Backend","seniority":"senior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Hyderabad, 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Validation","optional":false},{"name":"GDPR","optional":true},{"name":"HIPAA","optional":true}],"status":"live","first_seen_at":"2026-10-23T10:00:38Z","employer_posted_date":null,"last_verified_at":"2026-10-23T10:00:38Z","board_verified":false,"closed_at":null,"days_open":5,"trust":{"level":"not_scored","repost_count":null,"flags":[],"days_open":5},"description":"Senior Software V&V Engineer | Medical Devices | Hyderabad\n\nExperience: 10 - 18 Years\n\nLocation: Hyderabad\n\nIndustry: Medical Devices / Healthcare Technology\n\nEmployment Type: Full-Time\n\nHiring Initiative : Diversity Hiring | Women Professionals Encouraged to Apply\n\nJob Description :\n\nWe are hiring an experienced Senior Software Verification & Validation (V&V) Engineer for a leading organization in the medical technology sector.\n\nThe ideal candidate will have strong expertise in software testing, automation framework development, and regulatory compliance within a medical device software environment.\n\nKey Responsibilities :\n\n- Lead end-to-end software verification and validation activities across web, mobile, cloud, and integrated software platforms.\n\n- Develop and implement effective test strategies, test plans, and automated testing frameworks.\n\n- Ensure compliance with medical device software standards, including IEC 62304, ISO 13485, and applicable FDA regulations.\n\n- Manage requirements traceability, verification documentation, defect analysis, and test reporting.\n\n- Perform functional, integration, system, and regression testing.\n\n- Collaborate with development, product engineering, and quality teams to ensure software reliability and regulatory compliance.\n\n- Identify opportunities to improve test automation, testing processes, and overall software quality.\n\n- Provide technical guidance and mentoring to engineering teams.\n\nRequired Skills & Qualifications :\n\n- 10+ years of experience in Software Testing, Software Verification & Validation, or Quality Engineering.\n\n- Minimum 3 years of experience in regulated medical device software development or testing.\n\n- Strong knowledge of IEC 62304, ISO 13485, and FDA 21 CFR Part 820.\n\n- Hands-on experience in automation testing using PyTest, Playwright, Jest, REST Assured, or similar frameworks.\n\n- Proficiency in Python, JavaScript, or TypeScript.\n\n- Experience in medical device software V&V, requirements traceability, risk assessment, and defect management.\n\n- Strong analytical, documentation, and stakeholder collaboration skills.\n\nPreferred Skills :\n\n- Cloud-native applications and microservices testing.\n\n- API, mobile application, and web application testing.\n\n- Hardware-software integration and connected device testing.\n\n- Knowledge of HIPAA, GDPR, and regulated software development practices.\n\nSkills\nPython, RESTful API, HIPAA, Jest Framework, Medical Devices Integration, Physical Verification, Verification, System 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