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Hiring companyAmgen

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Sr Associate IS Analyst – Veeva Vault Quality

Hyderabad, India Full-time On-site

About the role

Amgen is seeking a Sr Associate IS Analyst – Veeva Vault Quality to join its Hyderabad team. The role focuses on designing, developing, and maintaining software applications for Amgen’s Veeva Vault Quality platform. Responsibilities include rapid prototyping, day‑to‑day operations, system integration, and ensuring performance and availability of critical systems. The analyst will translate functional and technical requirements into architecture, develop unit and integration tests, and follow GxP validation and risk‑based validation methodology. Collaboration with product managers, designers, QA, and cross‑functional teams is essential. The position requires strong knowledge of Veeva Vault Quality, Veeva configuration, Quality Docs, QMS, and Veeva Vault Manager, as well as experience in global pharmaceutical environments, GxP regulated projects, SDLC, Agile/Scrum, Python, JavaScript, Git, and SQL. The role also involves building custom solutions on Veeva Vault Platform, managing change controls, and maintaining documentation. Candidates must hold a Master’s, Bachelor’s, or Diploma in Computer Science, IT or related field with 1‑3, 3‑5, or 7‑9 years of experience respectively. Preferred certifications include Veeva Vault Platform Administrator and SAFe for Teams. Shift work may include evening or night shifts.

What you’ll do

  • Possesses strong rapid prototyping skills and can quickly translate concepts into working code.
  • Lead day to day operations and maintenance of Amgen’s Veeva Vault Quality and hosted applications.
  • Stay updated with the latest trends, advancements and standard processes for Veeva Vault Platform ecosystem.
  • Design, develop, and implement applications and modules, including custom reports, SDKs, interfaces, and enhancements.
  • Analyze and understand the functional & technical requirements of applications, solutions and systems, translate them into software architecture and design specifications.
  • Develop and execute unit tests, integration tests, and other testing strategies to ensure the quality of the software following IS change control and GxP Validation process while exhibiting expertise in Risk Based Validation methodology.
  • Work closely with cross-functional teams, including product management, design, and QA, to deliver high-quality software on time.
  • Maintain detailed documentation of software designs, code, and development processes.
  • Work on integrating with other systems and platforms to ensure seamless data flow and functionality.
  • Stay up to date on Veeva Vault Features, new releases and best practices around Veeva Platform Governance.

What you’ll bring

  • Master’s degree and 1 to 3 years of Computer Science, IT or related field experience OR
  • Bachelor’s degree and 3 to 5 years of Computer Science, IT or related field experience OR
  • Diploma and 7 to 9 years of Computer Science, IT or related field experience

Nice to have

SAFe for Teams (Preferred)

Skills

Experience with Veeva Vault Quality, including Veeva configuration settings and custom builds.Strong knowledge of Quality Docs, QMS and Veeva Vault Manager applications and its related business processes.6-8 years of experience working in global pharmaceutical IndustrExperience in building configured and custom solutions on Veeva Vault Platform.Experience in managing systems, implementing and validating projects in GxP regulated environments.Extensive expertise in SDLC, including requirements, design, testing, data analysis, creating and managing change controls.Proficiency in programming languages such as Python, JavaScript etc.Strong understanding of software development methodologies, including Agile and Scrum.Experience with version control systems such as Git.