Veeva Clinical Software Engineer II

Bristol Myers Squibb EU Policy; Hyderabad; On-site; INR 1,500,000 - 2,500,000; Full time

Job summary

Bristol Myers Squibb in India is seeking a Software Engineer II focused on Veeva Quality/Regulatory/Clinical/Platform to drive delivery of the portfolio and ensure compliant, scalable solutions across Clinical and Platform domains.

You will mentor Veeva developers, collaborate with cross‑functional teams, and maintain validated systems and Vault components in a GMP‑aligned environment, contributing to patient‑focused outcomes.

Qualifications

• 5+ years' experience with validated systems (CSV).
• 3+ years Vault experience in Quality, Regulatory, Clinical and Platform domains.
• Experience with GMP and regulatory documentation processes.

Responsibilities

• Owns end-to-end accountability for technology assets in the Veeva domain.
• Mentor Veeva developers in Quality, Regulatory, Clinical and Platform in India center.

Skills

Leadership

Excellent communication

Cross-functional collaboration

Veeva White Belt

CSV (Computer System Validation)

Veeva Platform knowledge

Tools

Veeva Platform

Veeva Vault

Quality Management Systems

Job description

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. Software Engineer II Veeva Quality/ Regulatory/Clinical/ Platform Position Summary: The primary focus of this role is the delivery of the Veeva Clinical and Platform portfolio. This position is responsible for the planning and execution of assigned projects supporting Clinical and Platform, reporting to the Veeva Platform community lead in India center. This role will oversee/work in matrix setup with approximately 6+ FTE’s (Veeva developers and testers) and will have accountability to drive both implementation and operations of Veeva Clinical and Platform Capabilities working with internal teams, contractors and Veeva product team. Desired Candidate Characteristics:

• Have a strong commitment to a career in technology with a passion for healthcare
• Ability to understand the needs of the business and commitment to deliver the best user experience and adoption
• Able to collaborate across multiple teams
• Demonstrated leadership experience
• Excellent communication skills
• Innovative and inquisitive nature to ask questions, offer bold ideas and challenge the status quo
• Agility to learn new tools and processes
• Veeva White Belt certification
• 5+ years' experience with validated system Computer System Validation (CSV)
• 3+ years Quality, Regulatory, Clinical and Platform Vault experience
• Experience with GMP, Quality, Regulatory , Clinical Management System and Quality, Regulatory, Clinical and Platform Docs

Key Responsibilities:

• Owns end-to-end accountability for managing technology assets, ensuring they are reliable, accessible, and secure
• Mentor group of Veeva Developers in Quality, Regulatory , Clinical and Platform domain in India center