Lilly MD IDS - Application Support Lead - 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.
Medicines Development Information and Digital Solutions (MD IDS) serves as a strategic function within Lilly Research Laboratories (LRL) partnering with the Medicines Development Unit (MDU). The MDU focuses on taking potential marketable products from Research through product registration and approval.
MD IDSMD IDS focuses on the MDU business needs of the future, enabling improvements through information and technology solutions. The teams define and influence information and business strategies, design and develop solutions to achieve the strategic outcomes, and ensure reliable deployment and support of these solutions.
The role of the MD IDS Application Support Lead acts as the primary, knowledgeable individual for a portfolio of IT applications and/or services in the Global Regulatory Affairs. This role works with a variety of resources to tactically maintain their applications within service levels, is well versed in the business processes, technologies including software-as-a-service, cloud data integration, data migration and assists in the management of vendor/user relationships tied to the applications and services. They engage with business partners, vendors, external service providers, and IDS partners to enhance and maintain the value and stability of the MD IDS application portfolio.
Key Objectives and Deliverables:
Business Analysis and Technical Integration
Works with internal partners and external suppliers in ensuring that Global Regulatory Affairs deliver maximum business value, remain technically advanced, quality complaint, sustainable and cost effective.
Develops in-depth business knowledge and strong relationships with business and IDS partners
Focuses on business processes and technical aspects to evaluate and translate functional requirements into technical requirements
Produces and maintains project documentation as required, including that of Computer Systems Quality
Understands the application (new and legacy) data models and coordinates migration of data from legacy to new applications using various data migration tools and platforms.Modifies existing systems or integrates packaged systems with existing infrastructure to meet business requirements
Ensures Lilly information assets are protected from malicious content and access to information is restricted to authorized personnel only
Designs, implements and manages the Service Level Management process to deliver the end-to-end IT service at a level that supports the business need and requirements
Leads and manages system enhancement projects including understanding and determining business impact, quantifying resource needs, and evaluating technical options
Collects and analyzes relevant information to resolve incidents, problem tickets, and change requests (CRs) within committed service levels, and in accordance with local procedures
Engages in continuous improvement through annual reviews of the Service Level Management process
Assists support vendor and Lilly management with the management of support vendor resources and daily operational activities
Incorporates ITIL methodology and best practices into support and service activities and deliverables
Partners on various other support activities including audits, Periodic Reviews, and other CAPA tasks
Required Technical Skills: Working knowledge of Veeva Vault, Oracle Database, PL/SQL and Java.
- Bachelor’s Degree
2+ years knowledge of the software development life cycle, spanning the entire lifecycle from project initiation to deployment, support, and retirement
Experience with supporting enterprise wide Cloud applications such as Salesforce or Veeva
Familiarity with ITIL Foundations framework
Familiarity with Software Quality Assurance methods and techniques
Experience with Global Regulatory Affairs business processes
Excellent oral and written communication skills
Excellent self-management skills
Demonstrated initiative to build relationships, learn new business processes, technologies and identify opportunities
Ability to achieve results through self and others
Ability to influence peers
Broad and deep technology learning agility
Lilly is an EEO/Affirmative Action Employer and 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.
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.
At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people. We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!