Career Opportunities: Developer (108028)
Job Summary
Veeva
Overview of the Role
As a Veeva Testing Specialist, you will play a pivotal role in ensuring the quality and compliance of Veeva-based solutions for clients in the pharmaceutical and life sciences sector. Your expertise will directly support the delivery of reliable, high-performing, and regulatory-compliant systems, aligning with HCLTech’s commitment to client success and innovation. This role is integral to streamlining business processes and improving outcomes for global life sciences organizations.
Detailed Responsibilities
· Design, develop, and execute comprehensive test plans, test cases, and test scripts for Veeva applications, with a focus on pharmaceutical industry requirements.
- Perform functional, regression, integration, and user acceptance testing (UAT) for Veeva Vault and related modules.
- Collaborate closely with business analysts, developers, and project managers to understand solution requirements and translate them into effective testing strategies.
- Identify, document, and track defects, working with development teams to ensure timely resolution.
- Ensure all testing activities are compliant with GxP, 21 CFR Part 11, and other applicable regulatory standards.
- Participate in test automation initiatives and leverage testing tools to improve efficiency and coverage.
- Prepare and maintain high-quality test documentation and reports for internal stakeholders and client audits.
- Support release management and deployment activities by validating changes and enhancements in the Veeva environment.
Skill Requirements
· Bachelor’s degree in Computer Science, Information Technology, Life Sciences, or a related field.
- Minimum 3 years of hands-on experience in testing Veeva Vault applications, preferably within the pharmaceutical or life sciences domain.
- Strong understanding of software testing methodologies, tools, and best practices.
- Experience with GxP, 21 CFR Part 11, and other regulatory frameworks relevant to life sciences.
- Familiarity with test management and defect tracking tools (e.g., HP ALM, JIRA, Zephyr).
- Excellent analytical, problem-solving, and communication skills.
- Ability to work independently and collaboratively in a fast-paced, global team environment
Key Responsibilities
2. To maintain the existing project by resolving/troubleshooting/debugging issues occurring in the existing project/application.
3. To understand client requirements and accordingly develop code to create required features.
4. Documentation of work.
Skill Requirements
Other Requirements
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Job Summary
Veeva
Overview of the Role
As a Veeva Testing Specialist, you will play a pivotal role in ensuring the quality and compliance of Veeva-based solutions for clients in the pharmaceutical and life sciences sector. Your expertise will directly support the delivery of reliable, high-performing, and regulatory-compliant systems, aligning with HCLTech’s commitment to client success and innovation. This role is integral to streamlining business processes and improving outcomes for global life sciences organizations.
Detailed Responsibilities
· Design, develop, and execute comprehensive test plans, test cases, and test scripts for Veeva applications, with a focus on pharmaceutical industry requirements.
- Perform functional, regression, integration, and user acceptance testing (UAT) for Veeva Vault and related modules.
- Collaborate closely with business analysts, developers, and project managers to understand solution requirements and translate them into effective testing strategies.
- Identify, document, and track defects, working with development teams to ensure timely resolution.
- Ensure all testing activities are compliant with GxP, 21 CFR Part 11, and other applicable regulatory standards.
- Participate in test automation initiatives and leverage testing tools to improve efficiency and coverage.
- Prepare and maintain high-quality test documentation and reports for internal stakeholders and client audits.
- Support release management and deployment activities by validating changes and enhancements in the Veeva environment.
Skill Requirements
· Bachelor’s degree in Computer Science, Information Technology, Life Sciences, or a related field.
- Minimum 3 years of hands-on experience in testing Veeva Vault applications, preferably within the pharmaceutical or life sciences domain.
- Strong understanding of software testing methodologies, tools, and best practices.
- Experience with GxP, 21 CFR Part 11, and other regulatory frameworks relevant to life sciences.
- Familiarity with test management and defect tracking tools (e.g., HP ALM, JIRA, Zephyr).
- Excellent analytical, problem-solving, and communication skills.
- Ability to work independently and collaboratively in a fast-paced, global team environment
Key Responsibilities
2. To maintain the existing project by resolving/troubleshooting/debugging issues occurring in the existing project/application.
3. To understand client requirements and accordingly develop code to create required features.
4. Documentation of work.