Job Summary

SysTechCare Support is seeking a highly detail-oriented and analytical Software Validation Specialist to join our In-House Quality Assurance Team. This role involves validating software systems for functionality, accuracy, and compliance with internal standards and industry regulations. You will collaborate with developers, business analysts, and QA engineers to ensure our applications meet the highest standards of quality before release.

Key Responsibilities

• Conduct software validation and verification activities throughout the software development lifecycle.

• Design, document, and execute test cases based on functional requirements and specifications.

• Identify, document, and report software defects using issue-tracking tools (e.g., JIRA, Bugzilla).

• Collaborate with cross-functional teams including developers, testers, and project managers to resolve validation issues.

• Ensure software compliance with regulatory guidelines (e.g., FDA 21 CFR Part 11, ISO standards if applicable).

• Maintain validation documentation and ensure traceability from requirements to testing.

• Participate in risk assessments and root cause analysis for validation-related concerns.

• Assist in internal and external audits by providing relevant validation documentation and insights.

Required Skills and Qualifications

• Bachelors degree in Computer Science, Information Technology, Engineering, or a related field.

• Strong knowledge of software validation methodologies, testing principles, and regulatory compliance standards.

• Familiarity with validation tools and test management systems.

• Excellent documentation and communication skills.

• Analytical mindset with a keen eye for detail.

• Proficiency in test scripting or automation is a plus.

Experience

• Minimum 3 to 5 years of experience in software validation, QA testing, or a similar role within regulated environments.

• Prior experience working in agile development teams or regulated industries such as healthcare, pharmaceuticals, or finance is preferred.

Working Hours

• Full-time | Monday to Friday

• 9:00 AM – 6:00 PM IST (with flexibility based on project needs)

Knowledge, Skills, and Abilities

• Deep understanding of software development life cycle (SDLC) and validation lifecycle (VLC).

• Strong organizational and problem-solving abilities.

• Ability to work independently and manage multiple validation tasks in parallel.

• Understanding of compliance frameworks like GxP, ISO 9001, or IEC 62304 is advantageous.

• Proficient in Microsoft Office Suite, especially Excel and Word for validation documentation.

Benefits

• Competitive salary and performance bonuses

• Comprehensive health insurance (self + dependents)

• In-house training and certification programs

• Paid time off, including sick leave and holidays

• Collaborative and inclusive work culture

• Access to the latest QA tools and software infrastructure

• Employee wellness programs and engagement activities

Why Join SysTechCare Support?

At SysTechCare Support, we do not just build software — we build trust. As a Software Validation Specialist, you will play a critical role in safeguarding product quality and user confidence. Be part of an innovative QA team where your contributions directly impact real-world applications and client satisfaction. We value growth, integrity, and excellence — and we are looking for people who do too.

How to Apply

If you are passionate about software quality and want to contribute to mission-critical projects, we invite you to apply. Please send your updated resume and a brief cover letter detailing your experience to:
📧 careers@systechcaresupport.com
or apply directly via our careers page: www.systechcaresupport.com/careers