Apply for Sr Associate IS Analyst Veeva Vault Quality at Amgen 2026. Check eligibility, salary, skills, and application process now.
Introduction
The Sr Associate IS Analyst – Veeva Vault Quality at Amgen is an excellent opportunity for experienced IT and pharma professionals looking to work at the intersection of technology and life sciences. This role focuses on managing and enhancing Veeva Vault Quality systems, ensuring compliance in GxP environments, and delivering scalable digital solutions. If you have strong experience in Veeva Vault and pharmaceutical systems, this position can significantly boost your career.
Job Overview
| Details | Information |
|---|---|
| Job Title | Sr Associate IS Analyst – Veeva Vault Quality |
| Company Name | Amgen |
| Location | Hyderabad, India |
| Employment Type | Full-Time |
| Department | Information Systems / IT |
| Experience Required | 5–9 Years |
| Education | Bachelor’s / Master’s Degree (IT, CS, or related field) |
| Salary | As per company norms |
Company Overview
Amgen is a globally recognized biotechnology company known for developing innovative therapies to treat serious illnesses. With over four decades of scientific leadership, the company combines advanced biology and technology to improve patient outcomes. Amgen continues to lead the biotech industry through cutting-edge research, digital transformation, and patient-focused innovation.
Job Location & Employment Type
This is a full-time, on-site role based in Hyderabad, India. Candidates should be flexible to work in different shifts, including evening or night shifts, depending on project requirements.
Open Positions / Department Details
The position is part of the Information Systems (IS) team, specifically working with:
- Veeva Vault Quality systems
- Quality Management Systems (QMS)
- GxP-regulated IT environments
- Enterprise software development and support
Key Roles & Responsibilities
Core Responsibilities
- Manage and maintain Veeva Vault Quality applications and systems
- Develop and implement custom modules, reports, and integrations
- Ensure system performance, availability, and reliability
- Translate business requirements into technical solutions
Development & Technical Work
- Design scalable software solutions and architecture
- Develop applications using programming languages like Python and JavaScript
- Perform unit testing, integration testing, and validation processes
- Work with APIs and system integrations for seamless data flow
Quality & Compliance
- Ensure compliance with GxP validation processes
- Follow risk-based validation methodologies
- Manage change controls and documentation within SDLC
- Maintain detailed technical and system documentation
Collaboration & Operations
- Work with cross-functional teams including QA, product, and engineering
- Monitor system health and resolve incidents promptly
- Stay updated with Veeva Vault platform updates and best practices
- Support global teams and participate in technical discussions
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in:
- Computer Science
- Information Technology
- Engineering or related field
Experience
- 5 to 9 years of experience in IT or related domain
- Strong experience in pharmaceutical or life sciences industry
- Hands-on experience with Veeva Vault Quality systems
Skills Required
Must-Have Skills
- Expertise in Veeva Vault Quality and configuration
- Strong understanding of QMS and quality processes
- Experience in GxP regulated environments
- Knowledge of SDLC and validation processes
- Programming skills (Python, JavaScript)
- Familiarity with Agile and Scrum methodologies
- Experience with Git or version control systems
Good-to-Have Skills
- Knowledge of databases (MySQL, SQL Server, PostgreSQL)
- Experience with ETL tools like Informatica or Databricks
- API integration experience (e.g., MuleSoft)
- Proficiency in SQL queries
- Experience with reporting tools like Power BI, Tableau, Spotfire
Salary & Benefits
- Salary: As per company norms
- Benefits may include:
- Health insurance and employee benefits
- Career growth opportunities in a global biotech company
- Exposure to advanced digital and pharmaceutical systems
- Learning and certification support
Selection Process
The hiring process generally includes:
- Online application submission
- Resume shortlisting
- Technical interview (Veeva Vault & IT skills)
- HR discussion
- Final selection
How to Apply
Interested candidates should apply online through the official Amgen careers portal. Make sure your resume highlights relevant Veeva Vault experience, IT skills, and pharmaceutical domain knowledge.
Important Dates
- Application Start Date: Already Open
- Last Date to Apply: Not mentioned (Apply early for better chances)
Why Apply for This Job?
The Sr Associate IS Analyst – Veeva Vault Quality at Amgen role offers strong career growth in both IT and pharmaceutical sectors. Here’s why you should consider applying:
- Work with a leading global biotechnology company
- Gain expertise in Veeva Vault, a highly in-demand platform
- Opportunity to work on global projects and systems
- Exposure to regulatory and GxP-compliant environments
- Competitive salary and long-term career stability
This role is ideal for professionals aiming to specialize in pharma IT systems and digital transformation.
FAQs
1. What experience is required for this role?
Candidates need 5–9 years of IT experience, preferably in pharmaceutical or life sciences domains.
2. Is Veeva Vault experience mandatory?
Yes, hands-on experience with Veeva Vault Quality is required.
3. What is the job location?
The position is based in Hyderabad, India.
4. What programming skills are needed?
Knowledge of Python, JavaScript, and SQL is important.
5. How can I apply for this job?
You can apply through Amgen’s official careers website.
Conclusion
The Sr Associate IS Analyst – Veeva Vault Quality at Amgen 2026 is a high-value opportunity for experienced professionals in pharma IT. With strong exposure to Veeva systems, regulatory environments, and global projects, this role can significantly enhance your technical and industry expertise. Apply early to secure your chance in this competitive position.
Disclaimer
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