Manager, Vault Quality Test Engineer

EyeBio; Hyderabad; Hybrid; INR 8,00,000 - 15,00,000; Full time

Job summary

A leading healthcare company in Hyderabad is seeking a skilled professional for the Vault Quality DevOps role. You will design, develop, and execute test plans to validate Veeva Vault Quality processes and ensure compliance. The ideal candidate has significant experience in software testing, especially within Quality Management Systems. This position offers the opportunity for hybrid work arrangements and supports continuous improvement efforts.

Benefits

Flexible Work Arrangements

Qualifications

• Proven experience in software testing.
• Hands-on experience testing Veeva Vault Quality or similar platforms.
• Strong knowledge of Quality processes like CAPA and Audits.

Responsibilities

• Design, develop, and execute test plans and cases.
• Execute manual and automated testing.
• Perform User Acceptance Testing (UAT) coordination.

Skills

Software testing

Quality Management Systems

Analytical skills

Communication skills

Tools

JIRA/XRAY

Automated testing tools

Job description

Overview

Vault Quality DevOps - Perform technical analysis, regression & automation testing

Role Overview

Design, develop, and execute test plans and test cases to validate Veeva Vault Quality processes. Ensure the quality, functionality, and compliance of Veeva Vault applications through rigorous testing. Collaborate with Quality, Business Analysts, Developers, and Administrators to support system enhancements, upgrades, and validations.

Key Responsibilities

• Develop comprehensive test strategies, test plans, and test cases based on business and functional requirements for Veeva Vault Quality processes (e.g., QualityDocs, Audit, Issues, Inspections, Complaints, Change Control).
• Execute manual and automated testing to validate system functionality, workflows, and integrations.
• Perform User Acceptance Testing (UAT) coordination and support end-users during testing phases.
• Identify, document, and track defects and issues using defect tracking tools; work closely with development and support teams to resolve them.
• Participate in system validation activities ensuring compliance with regulatory standards such as FDA 21 CFR Part 11 and GxP.
• Review and validate system configurations, workflows, and metadata changes in Veeva Vault.
• Collaborate with cross-functional teams to understand system changes and their impact on Quality Operations.
• Maintain detailed test documentation including test scripts, test results, and validation reports.
• Support release management activities by validating patches, upgrades, and new feature deployments.
• Assist in continuous improvement of testing processes and tools to enhance efficiency and coverage.

Required Skills and Qualifications

• Proven experience in software testing, preferably in Quality Management Systems or regulated environments.
• Hands-on experience testing Veeva Vault Quality or similar cloud-based QMS platforms.
• Strong knowledge of Quality processes such as CAPA, Change Control, Document Management, and Audits.
• Familiarity with regulatory compliance requirements (FDA 21 CFR Part 11, GxP).
• Experience using JIRA/XRAY for test case management, test execution, reporting, defect management within Agile environments.
• Ability to write clear, concise, and comprehensive test plans and test cases.
• Strong analytical and problem-solving skills.
• Excellent communication skills to coordinate with technical and business teams.
• Detail-oriented with a focus on quality and compliance.

Preferred Qualifications

• Experience with automated testing tools and scripting.
• Veeva Certifications (Vault Quality Suite/ QMS). The role holder has completed the Certified Vault Training and is up to date
• Background in pharmaceutical, biotech, or medical device industries.
• Knowledge of Agile or other software development methodologies.
• Experience in system validation and documentation in regulated environments.

Who we are

We are known as Merck & Co., Inc., Rahway, New Jersey, USA in the United States and Canada and MSD everywhere else. For more than a century, we have been inventing for life, bringing forward medicines and vaccines for many of the world\'s most challenging diseases. Today, our company continues to be at the forefront of research to deliver innovative health solutions and advance the prevention and treatment of diseases that threaten people and animals around the world.

What we look for

Imagine getting up in the morning for a job as important as helping to save and improve lives around the world. Here, you have that opportunity. You can put your empathy, creativity, digital mastery, or scientific genius to work in collaboration with a diverse group of colleagues who pursue and bring hope to countless people who are battling some of the most challenging diseases of our time. Our team is constantly evolving, so if you are among the intellectually curious, join us—and start making your impact today.

Additional Information

• Employee Status: Regular
• Relocation:
• VISA Sponsorship:
• Travel Requirements:
• Flexible Work Arrangements: Hybrid
• Shift:
• Valid Driving License:
• Hazardous Material(s):
• Job Posting End Date: 10/22/2025

A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.