Veeva Clinical Software Engineer II

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 * Leads operational activities such as maintenance and break-fix releases, security assessments, regulatory risk assessments, incident response, etc. * Manages the build, run of technology assets, and ensures timely delivery of releases (Veeva Vault General Releases, Operational Releases, and Project Releases) * Collaborates closely with the Veeva Drug Development & Quality , Regulatory , Clinical and Platform Cloud team to obtain a working knowledge of the Veeva Vault platform and the various domain-specific Vaults * Partners with IT Business Partners and Business Subject Matter Experts to define, plan for, prioritize, deliver, and support the systems and ensure maximum value is achieved * Ability to understand, prioritize, and communicate IT needs to our business colleagues and stakeholders * Designs technical solutions to satisfy business requirements * Fulfills all approved, technology asset-specific business needs * Obtain/maintain a Veeva Associate Administrator Level certification Qualifications & Experience * Requires thorough knowledge of the principles and concepts of a discipline and developed knowledge of other related disciplines, typically gained through a university degree and 5-7 years of experience. Responsible for leading a small team (results/outcomes, goal setting, input into performance management and coaching). Actively...