Amgen is hiring a Sr Associate IS Analyst – Veeva Vault Quality for its Hyderabad location. This on-site, full-time role in Information Systems offers excellent opportunities for experienced professionals seeking pharma jobs in Veeva Vault configuration, GxP systems, and quality management within the biotechnology sector.
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About the Company
Amgen is a global biotechnology pioneer that harnesses biology and technology to develop innovative medicines for serious diseases. For over 40 years, Amgen has been at the forefront of biotechnology, using advanced technology and human genetic data to deliver therapies that improve patients’ lives.
The company focuses on cutting-edge research, manufacturing, and commercialization while maintaining the highest standards of quality and regulatory compliance. Amgen provides dynamic pharmaceutical careers in India with global exposure and a strong emphasis on innovation and scientific excellence.
Job Details
- Company Name: Amgen
- Experience: 5–9 years (5–7 years in global pharmaceutical industry preferred)
- Qualification: Bachelor’s or Master’s degree in Computer Science, IT, or related field
- Location: Hyderabad, Telangana, India
- Work Type: Full-time, On-site
Job Description
Amgen is seeking a Sr Associate IS Analyst – Veeva Vault Quality to join the Veeva Vault team. The role involves designing, developing, and maintaining software applications for Amgen’s Veeva Vault Quality platform, ensuring high availability, performance, and compliance in a GxP-regulated environment.
This position includes leading day-to-day operations, building custom solutions, and supporting validation processes while collaborating with global cross-functional teams.
Sr Associate IS Analyst – Veeva Vault Quality
- Department: Information Systems (IS)
- Job Family: Information Systems / Veeva Platform
- Market: Biotechnology / Pharmaceutical
- Role: Sr Associate IS Analyst – Veeva Vault Quality
- Experience: 5–9 years
- Education/Qualification: Bachelor’s or Master’s degree in Computer Science / IT or related field
Skills/Qualifications
- Must-Have:
- Strong experience with Veeva Vault Quality, including configuration, custom builds, Quality Docs, QMS, and Veeva Vault Manager
- 5–7 years in global pharmaceutical industry
- Experience in GxP-regulated environments with Risk-Based Validation and SDLC
- Proficiency in Python, JavaScript, or similar programming languages
- Experience with Agile/Scrum methodologies and Git version control
- Veeva Vault Platform Administrator Certification (or equivalent) – Must-Have
- Good-to-Have:
- Knowledge of relational databases (MySQL, SQL Server, PostgreSQL)
- Experience with ETL tools (Informatica, Databricks), API integrations (MuleSoft), SQL queries
- Familiarity with reporting tools (Tableau, Spotfire, Power BI)
- SAFe for Teams certification (preferred)
- Excellent analytical, troubleshooting, communication, and presentation skills
- Ability to work effectively in global, virtual teams
Key Responsibilities
- Lead day-to-day operations and maintenance of Amgen’s Veeva Vault Quality applications
- Design, develop, and implement custom reports, SDKs, interfaces, and enhancements
- Translate functional and technical requirements into software architecture and specifications
- Develop and execute unit, integration, and other tests following IS change control and GxP validation
- Collaborate with product managers, designers, QA, and cross-functional teams
- Integrate Veeva Vault with other systems for seamless data flow
- Stay updated on Veeva Vault features, releases, and platform governance best practices
- Automate operations, monitor system health, and respond to incidents
- Maintain detailed documentation of designs, code, and processes
- Support rapid prototyping and deliver high-quality solutions on time
Benefits/Perks
- Career growth in biotechnology IT and Veeva Vault expertise
- Exposure to global GxP-regulated projects and innovative drug development
- Collaborative environment with cutting-edge technology
- Opportunities for professional development and certifications
- Contribution to therapies that improve patients’ lives worldwide
- Inclusive workplace with equal opportunity and reasonable accommodations
How to Apply
Apply directly through the official Amgen Careers portal using Job Requisition ID R-231964.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Amgen Career page.
For more pharma jobs in Hyderabad, IT roles in Quality Systems, and biotechnology opportunities across India, visit Pharma Recruiter.
Apply now to join Amgen and advance your career in Veeva Vault Quality solutions!
Why You Should Join
Amgen offers a purpose-driven culture where your work directly supports the development and delivery of life-changing medicines. With a strong focus on innovation, compliance, and collaboration, the company provides long-term career stability, global exposure, and opportunities to work on advanced Veeva Vault implementations in a highly regulated pharmaceutical environment.
FAQs
What is the experience required for the Sr Associate IS Analyst – Veeva Vault Quality role?
5–9 years of experience, with 5–7 years preferred in the global pharmaceutical industry.
Is Veeva Vault certification mandatory?
Yes, Veeva Vault Platform Administrator or equivalent certification is a must-have.
What is the work location and shift for this position?
The role is On-site in Hyderabad and may require later/evening or night shifts based on business needs.
What educational qualification is needed?
Bachelor’s or Master’s degree in Computer Science, IT, or a related field.
