Senior Software V&V Engineer

Selective Global Search Pvt. Ltd.; Hyderabad; On-site; INR 4,000,000 - 7,000,000; Full time

Job summary

Selective Global Search Pvt. Ltd. in Hyderabad is seeking a Senior Software V&V / Test Automation Specialist to lead verification across complex applications, and to develop automation frameworks for web, mobile, and API testing.

The role emphasizes compliance with medical device software standards and requires strong experience in V&V activities. You will collaborate with engineering teams to improve software quality, manage test planning and regulatory documentation, and drive testing

Qualifications

• 10+ years in Software Testing / V&V.
• 3+ years in regulated medical device software.
• Knowledge of IEC 62304, ISO 13485, and FDA 21 CFR Part 820.
• Experience with regulatory documentation.

Responsibilities

• Lead software verification and validation activities across complex applications.
• Develop and enhance automation frameworks for web, mobile, and API testing.
• Manage test planning, requirements traceability, defect analysis, and validation documentation.
• Ensure compliance with applicable medical device software standards.
• Collaborate with engineering teams to improve software quality and testing efficiency.

Skills

Software Testing

Quality Engineering

V&V

Tools

PyTest

Playwright

Jest

REST Assured

Job description

We're Hiring | Senior Software V&V / Test Automation Specialist

Committed to Diversity & Inclusive Hiring

We are supporting a leading organization in identifying experienced professionals with strong expertise in Software Verification & Validation, Test Automation, and Medical Device Software Compliance.

Key Responsibilities:

• Lead software verification and validation activities across complex applications.
• Develop and enhance automation frameworks for web, mobile, and API testing.
• Manage test planning, requirements traceability, defect analysis, and validation documentation.
• Ensure compliance with applicable medical device software standards.
• Collaborate with engineering teams to improve software quality and testing efficiency.

Required Expertise:

• 10+ years in Software Testing / Quality Engineering / V&V.
• 3+ years of experience in regulated medical device software.
• Knowledge of IEC 62304, ISO 13485, and FDA 21 CFR Part 820.
• Experience with PyTest, Playwright, Jest, REST Assured, or similar automation tools.
• Strong understanding of software validation, risk management, and regulatory documentation.

Preferred:

• Experience in cloud platforms, microservices, connected devices, or hardware-software integration testing.

Committed to Diversity & Inclusive Hiring

#DiversityHiring #WomenInTech #WomenInEngineering #SoftwareValidation #MedicalDevices #TestAutomation #SDET #HyderabadJobs #Hiring