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Lilly MD IDS – Veeva RIM Developer (GRA) in Bengaluru, India

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 35,000 employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 39,000 employees work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the globe.

Medicines Development (MD) Information and Digital Solutions (IDS) serves as a strategic function within the Lilly Medicines Development Unit. There are tremendous opportunities in MD IDS as continued investments are made in the transformation associated with the next generation of drug development and the goals of a Digital MD. Global Regulatory Affairs is part of the MD IDS organization that supports the submissions and publishing process.

To help meet the increasing demand for Global Regulatory Affairs (GRA) capabilities within Lilly, we are looking to hire talented software full-stack developers in Lilly Capability Center in India. These developers will work on various projects in close partnership with the GRA capability team supporting the Medicines Development function.

Key Responsibilities:

  • Participates in the estimation of activities, owns technical implementation of the SaaS application, and responsible for the design, build, unit and integration testing for new and modified features of the RIM application. The RIM Developer has a keen focus to detail through ensuring RIM application is developed using the framework of the Veeva Vault configuration standards and best practices.

  • Works closely with business to understand the business requirements. Thinks critically to help them design the solution they need; not just the solution they think they need.

  • Participates in the requirements workshops, design, prototype, configure and document RIM solutions.

  • Implements Veeva RIM suite of application to meet the business, functional, security and integration requirements either via RIM configuration or custom development using Veeva Vault SDK

  • Participates in the testing and validation activities by helping in the creation and review of test scenarios, test executions and validation documents.

  • Works with the RIM support team to provide technical solutions to production issues.

Basic Qualifications :

  • Bachelor’s Degree (or equivalent work experience)

  • 5+ years of experience developing IT solutions in a SaaS environment of which 3+ years in Veeva RIM application configuration/development

  • Strong teamwork, self-management, problem-solving abilities

  • Excellent oral and written communication skills

  • Trained and Certified in Veeva Vault

Experience:

  • Experience working with or for Life Sciences companies; including, Pharmaceutical, Biotechnology, Healthcare, or Medical Device organizations with knowledge of drug development processes and regulatory submissions

  • System implementation experience either as a consultant, business, or IT representative for Veeva RIM application.

  • Experience working with Veeva Vault SDK to deliver custom solutions by extending the RIM application capabilities.

  • Deep understanding of Veeva RIM data model, data loader and migration tools and technologies

  • Understanding of health care regulations, international regulations, and privacy controls

Lilly is a global health care leader that unites caring with discovery to make life better for people around the world. For more than a century, we have stayed true to a core set of values—excellence, integrity, and respect for people—that guide us in all we do: discovering medicines that meet real needs, improving the understanding and management of disease, and giving back to communities. We also are committed to investing in our employees and supporting a culture of well-being —through competitive pay, comprehensive employee benefit programs, and training and development resources.

Lilly is an EEO/Affirmative Action Employer and does not discriminate based on age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability, or any other legally protected status.

Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( LillyRecruitingCompliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. Any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

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