Sr. Consultant

OPENTEXT - THE INFORMATION COMPANY

OpenText is a global leader in information management, where innovation, creativity, and collaboration are the key components of our corporate culture. As a member of our team, you will have the opportunity to partner with the most highly regarded companies in the world, tackle complex issues, and contribute to projects that shape the future of digital transformation.

AI-First. Future-Driven. Human-Centered.

At OpenText, AI is at the heart of everything we do—powering innovation, transforming work, and empowering digital knowledge workers. We're hiring talent that AI can't replace to help us shape the future of information management. Join us.

Impact

As a QA Expert, you will play a critical role in ensuring that E-Signature solutions delivered to Pharma and Life Sciences customers are high-quality, reliable, secure, and compliant with applicable regulatory requirements.

You will own and drive QA activities across customer projects, working closely with Consulting, Development, Product, SaaS, SQA, and customer teams. Your expertise will help ensure that solutions are thoroughly tested and validated before deployment, while proactively identifying risks and preventing production issues.

You will also contribute to improving QA processes, test automation, reusable test assets, and quality practices across the E-Signature consulting organization.

WHAT THE ROLE OFFERS

• Own and lead QA activities for E-Signature Pharma and Life Sciences customer projects.

• Define and execute test strategies, test plans, test scenarios, test cases, and test execution based on customer requirements.

• Perform functional, integration, regression, system, exploratory, and end-to-end testing of E-Signature solutions.

• Validate electronic signature workflows, approvals, audit trails, authentication, user access, and business rules.

• Ensure end-to-end traceability between requirements, test cases, defects, and test evidence.

• Support validation activities for regulated applications, including 21 CFR Part 11, EU Annex 11, GxP, CSV/CSA, and